InteractiveFly: GeneBrief

no receptor potential A : Biological Overview | Evolutionary Homologs | Regulation | Developmental Biology | Effects of Mutation | References


Gene name - no receptor potential A

Synonyms - phospholipase C

Cytological map position - 4B6

Function - 1-phosphatidylinositol-4,5-biphosphate phosphodiesterase

Keywords - Visual signal transduction, odor signal
transduction, testis

Symbol - norpA

FlyBase ID: FBgn0004625

Genetic map position - 1-6.5

Classification - phosphatidylinositol-specific phospholipase C

Cellular location - cytoplasmic



NCBI links: Precomputed BLAST | Entrez Gene

Recent literature
Yadav, S., Garner, K., Georgiev, P., Li, M., Gomez-Espinosa, E., Panda, A., Mathre, S., Okkenhaug, H., Cockcroft, S. and Raghu, P. (2015). RDGBα, a PI-PA transfer protein regulates G-protein coupled PtdIns(4,5)P2 signalling during Drosophila phototransduction. J Cell Sci. PubMed ID: 26203165
Summary:
Many membrane receptors activate phospholipase C (PLC) during signalling, triggering changes in the levels of several plasma membrane (PM) lipids including PtdIns, PtdOH and PtdIns4,5P2. It is widely believed that exchange of lipids between the PM and endoplasmic reticulum (ER) is required to restore lipid homeostasis during PLC signalling, yet the mechanism remains unresolved. RDGB is a multi-domain protein with a PITP domain (RDGB-PITPd). In vitro, RDGB-PITPd binds and transfers both PtdOH and PtdIns. In Drosophila photoreceptors that experience high rates of PLC activity, RDGB function is essential for phototransduction. Binding of PtdIns to RDGB-PITPd is essential for normal phototransduction; yet this property is insufficient to explain in vivo function since another Drosophila PITP (vib) that also binds PtdIns cannot rescue the phenotypes of RDGB deletion. In RDGB mutants, PtdIns4,5P2 resynthesis at the PM following PLC activation is delayed and PtdOH levels elevate. Thus RDGB couples the turnover of both PtdIns and PtdOH, key lipid intermediates during G-protein coupled PtdIns(4,5)P2 turnover.

Saint-Charles, A., Michard-Vanhée, C., Alejevski, F., Chélot, E., Boivin, A. and Rouyer, F. (2016). Four of the six Drosophila rhodopsin-expressing photoreceptors can mediate circadian entrainment in low light. J Comp Neurol [Epub ahead of print]. PubMed ID: 26972685
Summary:
Light is the major stimulus for the synchronization of circadian clocks with day-night cycles. The light-driven entrainment of the clock that controls rest-activity rhythms in Drosophila relies on different photoreceptive molecules. Cryptochrome (CRY) is expressed in most brain clock neurons whereas six different rhodopsins (RH) are present in the light-sensing organs. The compound eye includes outer photoreceptors that express RH1 and inner photoreceptors that each express one of the four RH3-6. In low light, the synchronization of behavioral rhythms relies on either CRY or the canonical rhodopsin phototransduction pathway, which requires the phospholipase C-β encoded by norpA (no receptor potential A). This study used norpAP24 cry02 double mutants that are circadianly blind in low light and restored NORPA function in each of the six types of photoreceptors, defined as expressing a particular rhodopsin. The NORPA pathway was less efficient than CRY for synchronizing rest-activity rhythms with delayed light-dark cycles but is important for proper phasing, whereas the two light-sensing pathways can mediate efficient adjustments to phase advances. Four of the six rhodopsin-expressing photoreceptors can mediate circadian entrainment and all are more efficient for advancing than for delaying the behavioral clock. These results thus reveal different contributions of rhodopsin-expressing photoreceptors and suggest the existence of several circuits for rhodopsin-dependent circadian entrainment.


BIOLOGICAL OVERVIEW

Visual excitation of vertebrate retinal photoreceptors begins with the absorption of light by the visual pigment (opsin), which is followed by activation of a G-protein, transducin. This results in activation of a photoreceptor-specific cGMP phosphodiesterase (PDE). Increased cGMP hydrolysis lowers the cytoplasmic cGMP concentration, which is believed to cause closure of the cGMP-gated ion (cyclic nucleotide gated or CNG) channel in the plasma membrane and the generation of an electrical response. In Drosophila, rhodopsin, acting through G proteins, targets the protein NorpA encoded by a phosphoinositide-specific phospholipase C (PLC). NorpA in turn catalyzes the breakdown of phospholipids and generates inositol trisphosphate (IP3) and diacylglycerol. Diacylglycerol is a potential precursor for several polyunsaturated fatty acids, such as arachidonic acid and linolenic acid. Both TRP (transient receptor potential) and TRPL (TRP-like) are cation channels that are activated in the visual transduction process. These two proteins share homology with alpha-subunits of voltage-gated calcium and sodium channels in vertebrates. Polyunsaturated fatty acids activate the Drosophila light-sensitive channels TRP and TRPL. Since arachidonic acid may not be found in Drosophila, it is suggested that another polyunsaturated fatty acid, such as linolenic acid, may be a messenger of excitation in Drosophila photoreceptors (Chyb, 1999).

Of special interest is evidence for functioning of the visual cascade in Drosophila testis. DGq is the alpha subunit of the heterotrimeric GTPase (G alpha), which couples rhodopsin to phospholipase C in Drosophila vision. Three duplicated exons were identified in dgq by scanning the GenBank data base for unrecognized coding sequences. These alternative exons encode sites involved in GTPase activity and G beta-binding, NorpA-binding, and rhodopsin-binding. In vivo splicing of dgq was examined in adult flies: in all regions, other than the male gonads, only two isoforms are expressed. One isoform, dgqA, is the original visual isoform and is expressed in eyes, ocelli, brain, and male gonads. The other, dgqB, has the three novel exons and is widely expressed. Remarkably, all three nonvisual B exons are highly similar (82% identity at the amino acid level) to domains of the Gq alpha family consensus, from Caenorhabditis elegans to human, but all three visual A exons are divergent (61% identity). Intriguingly, a third isoform, dgqC, is found that is specifically and abundantly expressed in male gonads, and shares the divergent rhodopsin-binding exon of dgqA. It is suggested that DGqC is a candidate for the light-signal transducer of a testes-autonomous photosensory clock. This proposal is supported by the finding that norpA is expressed in male gonads, as well as the photoreceptor-cell-specific genes rhodopsin 2 and arrestin 1 (Alvarez, 1996).

These observations suggest that the visual DGqA is generated by the duplication of three DGqB exons. This allows the photoreceptor-specific DGqA to be optimized for phototransduction at the Gbeta-interacting/GTPase site, the NorpA-binding site and the Rh binding site. That this specialization occurs is suggested by the existence of eye-specific forms of Gbeta, NorpA, and Rh in Drosophila. NorpA, for example, has two cloned isoforms that vary at one alternatively spliced exon: one (I) is expressed at high levels and appears to be eye-specific, and the other (II) is expressed at low levels throughout development and in various tissues -- head, thorax, abdomen, and legs (Kim, 1995). The visual norpA.I is not expressed in testes, but norpA.II is. Vertebrate sensory systems also show organ specific isoform adaptation: these systems have specialized Galphas (of non-q class) for rod-vision (Gt1alpha), cone-vision (Gt2alpha), olfaction (Golfalpha), and taste (Ggustalpha). However, squid, the only other invertebrate with a known Rh-linked (Gqalpha), uses a Galpha more similar to DGqB than to the visual DGqA. This suggests that before the divergence of squid and fly, there was a single DGqB-like Gqalpha that mediated vision and at least one other, even more ancient, signaling pathway (Alvarez, 1996).

A central problem in sensory system biology is the identification of the signal transduction pathways used in different sensory modalities. Odorant response in the maxillary palps olfactory organ of Drosophila (see Odorant Receptors), but not the response of the antennal olfactory cells, depends on the norpA phospholipase C gene, providing evidence for use of the inositol 1,4,5-trisphosphate (IP3) signal transduction pathway. Consistent with the demonstration of a role for norpA in the maxillary palp, but not the antenna, norpA is found to be expressed in the maxillary palp, but not the antenna. Staining is localized along the lateral surface of the maxillary palp, in a region that contains a high density of olfactory hairs. Staining occurs not only on cell bodies but also in axons (the maxillary nerve). Since the norpA gene is also essential to phototransduction, this work demonstrates overlap in the genetic and molecular underpinnings of vision and olfaction. Genetic and molecular data also indicate that some olfactory information flows through a pathway that does not depend on norpA. The maxillary palp response is not abolished in norpA null flies, suggesting the existence of an additional PLC independent pathway for the odorant response (Riesgo-Escovar, 1995).

Regulation of dual oxidase activity by the Galphaq-phospholipase Cbeta-Ca2+ pathway in Drosophila gut immunity

All metazoan guts are in constant contact with diverse food-borne microorganisms. The signaling mechanisms by which the host regulates gut-microbe interactions, however, are not yet clear. This study shows that phospholipase C-β (PLCβ) signaling modulates dual oxidase (DUOX) activity to produce microbicidal reactive oxygen species (ROS) essential for normal host survival. Gut-microbe contact rapidly activates PLCβ through Gαq, which in turn mobilizes intracellular Ca2+ through inositol 1,4,5-trisphosphate generation for DUOX-dependent ROS production. PLCβ mutant flies have a short life span due to the uncontrolled propagation of an essential nutritional microbe, Saccharomyces cerevisiae, in the gut. Gut-specific reintroduction of the PLCβ restores efficient DUOX-dependent microbe-eliminating capacity and normal host survival. These results demonstrate that the Gαq-PLCβ-Ca2+-DUOX-ROS signaling pathway acts as a bona fide first line of defense that enables gut epithelia to dynamically control yeast during the Drosophila life cycle (Ha, 2009).

All organisms are in constant contact with a large number of different types of microbes. This is especially true in the case of the gut epithelia, which control life-threatening pathogens as well as food-borne microbes. In addition to this microbe-eliminating capacity, gut epithelia also need to protect normal commensal microbes which are in a mutually beneficial relationship. Therefore, gut epithelia must be equipped to differentially operate innate immunity in order to efficiently eliminate life-threatening microbes while protecting beneficial microbes. Studies using Drosophila as a genetic model have greatly enhanced understanding of the microbe-controlling mucosal immune strategy in gut epithelia. Previous studies in a gut infection model using oral ingestion of pathogens revealed that the redox system has an essential role in host survival by generating microbicidal effectors such as reactive oxygen species (ROS) (Ha, 2005a; Ha, 2005b). In this redox system, dual oxidase (DUOX), a member of the nicotinamide adenine dinucleotide phosphate (NADP)H oxidase family, is responsible for the production of ROS in response to gut infection (Ha, 2005a). Following microbe-induced ROS generation, ROS elimination is assured by immune-regulated catalase (IRC), thereby protecting the host from excessive oxidative stress (Ha, 2005b). In addition to the redox system, the mucosal immune deficiency (IMD)/NF-κB signaling pathway, which leads to the de novo synthesis of microbicidal effector molecules such as antimicrobial peptides (AMPs), has an essential complementary role to the redox system when the host encounters ROS-resistant pathogenic microbes. These findings indicate that the different spectra of microbicidal activity encompassed by ROS and AMPs may provide the versatility necessary for Drosophila gut immunity to control microbial infections. Furthermore, in the absence of gut infection, a selective repression of IMD/NF-κB-dependent AMPs is mediated by the homeobox gene Caudal, which is required for protection of the resident commensal community and host health. Therefore, fine-tuning of different gut immune systems appears to be essential for both the elimination of pathogens and the preservation of commensal flora (Ha, 2009).

Most studies evaluating gut immunity have been performed in an oral infection model in which the pathogens are ingested. However, the gut epithelia constitute the interface between the host and the microbial environment; therefore, it is likely that animals in nature have already been subjected to continuous microbial contact, even in the absence of oral infection. Thus, it is essential to determine the mechanism by which this natural and continuous microbial interaction produces ROS at a tightly controlled, yet adequate level that allows for healthy gut-microbe interactions and gut homeostasis, because deregulated generation of ROS is believed to lead to a pathophysiologic condition in the gut epithelia. Although the DUOX system is of central importance in gut immunity, the signaling pathway(s) by which gut epithelia regulate DUOX-dependent microbicidal ROS generation are poorly understood (Ha, 2009).

Drosophila feed on microbes, and one of their most essential microbial food sources is baker's yeast, Saccharomyces cerevisiae. As early as 1930, yeast was discovered to be an essential nutrient source for Drosophila and is now used as a major ingredient in standard laboratory Drosophila food recipes. Further, Drosophila-Saccharomyces interaction occurs in wild-captured Drosophila, which suggests that this interaction is an evolutionarily ancient natural phenomenon. Although many studies have investigated the effect of yeast on Drosophila metabolism and aging, very few works have been reported on the effect of yeast in terms of the host immunity. Specifically, it has previously been shown that dietary yeast contributes to the cellular immune responsiveness of Drosophila against a larval parasitoid, Leptopilina boulardi. However, the relationship between yeast and Drosophila gut immunity during the normal life cycle has never been closely examined. Therefore, in this study, a Drosophila-yeast model was used to investigate the intracellular signaling pathway by which the host mounts mucosal antimicrobial immunity, as well as the in vivo value of this pathway in the host's natural life. Through biochemical and genetic analyses, this study revealed that the Gαq-mediated phospholipase C-β (PLCβ) pathway is involved in the routine control of dietary yeast in the Drosophila gut. PLCβ is dynamically activated in the presence of ingested yeast and subsequently mobilizes the intracellular Ca2+ to produce ROS in a DUOX-dependent manner. The presence of all of these signaling components of the Gαq-PLCβ-Ca2+-DUOX-ROS pathway in the gut is essential to ensure routine control of dietary yeast and host fitness, highlighting the importance of this immune signaling as a bona fide first line of defense in Drosophila (Ha, 2009).

This study demonstrates that the Gαq-PLCβ-Ca2+ signaling pathway controls the mucosal gut epithelial defense system through DUOX-dependent ROS generation, which is responsible for routine microbial interactions in the gut epithelia in the absence of infection. The PLCβ pathway impacts a wide variety of biological processes through the generation of a lipid-derived second messenger. In this process, the hydrolysis of a minor membrane phospholipid, phosphatidylinositol 4,5-bisphosphate, by PLCβ generates two intracellular messengers, IP3 and diacylglycerol. This process is one of the earliest events through which more than 100 extracellular signaling molecules regulate functions in their target cells. It has been shown that Gαq-PLCβ signaling is essential for the activation of the phototransduction cascade in Drosophila. This study revealed a physiological role of PLCβ wherein it is involved in the regulation of DUOX enzymatic activity, which leads to the generation of microbicidal ROS in the mucosal epithelia (Ha, 2009).

PLCβ signaling is very rapid, with only a few seconds necessary to activate Ca2+ release and ROS production. This rapid response may be advantageous for the host and may be the mechanism by which dynamic and routine control of microbes in the gut epithelia is achieved. Because the gut is in continuous contact with microbes such as dietary microorganisms, it is conceivable that under normal conditions routine microbial contact dynamically induces a certain level of basal Gαq-PLCβ activity that varies depending on the local microbe concentration. This basal Gαq-PLCβ-DUOX activity seems to be sufficient for host survival. In such conditions of low bacterial burden, NF-κB-dependent AMP expression is known to be largely repressed by Caudal repressor for the preservation of commensal microbiota (Ryu, 2008). However, in the case of high bacterial burden (e.g., gut infection condition), the DUOX-ROS system would be strongly activated for full microbicidal activity. Furthermore, all of the flies that contained impaired signaling potentials for the Gαq-PLCβ-Ca2+-DUOX pathway were totally intact following septic injury but short-lived under natural rearing conditions or under gut infection conditions, indicating that the mucosal immune pathway is distinct from the systemic immune pathway (Ha, 2009).

It is not clear how Gαq- and PLCβ-induced Ca2+ modulates DUOX enzymatic activity. Because the DUOX lacking Ca2+-binding EF hand domains is unable to rescue the DUOX-RNAi flies (Ha, 2005a), it is plausible that Ca2+ directly modulates the enzymatic activity of DUOX through binding to the EF hand domains (Ha, 2009).

It is also important to determine what pathogen-associated molecular patterns (PAMPs) are responsible for the activation of PLCβ signaling. In Drosophila, peptidoglycan and β-1,3-glucan are the only two PAMPs known to induce the NF-κB signaling pathway in the systemic immunity. The results showed that neither peptidoglycan nor β-1,3-glucan was able to induce ROS in S2 cells, which suggests that a previously uncharacterized type(s) of PAMP is involved in the mucosal immunity. Because the Gαq protein acts as an upstream signaling component of the PLCβ-Ca2+ pathway, a microbe-derived ligand capable of activating G protein coupled receptor(s) and/or Gαq protein may be the best candidate for the Gαq-PLCβ-Ca2+-DUOX signaling pathway. Given the broad spectrum of microbes that activate the response, it remains possible that the unknown upstream sensors resemble a stress response more than a PAMP response. Elucidation of the molecular nature of such agonists will greatly enhance understanding of bacteria-modulated redox signaling in the gut epithelia. In conclusion, this study demonstrates that mucosal epithelia have evolved an innate immune strategy, which is functionally distinct from the NF-κB-dependent systemic innate immune system. The rapid Gαq-PLCβ-Ca2+-DUOX signaling is adapted to the routine and dynamic control of gut-associated microbes and may impact the long-term physiology of the intestine and host fitness (Ha, 2009).


REGULATION
Promoter Structure

The 5'-flanking region of the Drosophila melanogaster norpA gene has been sequenced and its promoter characterized. The potential promoter region, which was deduced from the determination of the transcription start point (tsp), lacks a distinct TATA box sequence. Deletion analysis of the promoter region suggests that the minimal promoter necessary for efficient expression of the gene is located between -138 (PstI) and +278 relative to the tsp. Within this minimal promoter region, at least two downstream regulatory elements responsible for the stimulation of gene expression seem to exist in the DNA fragments between +44 and +121 and between +214 and +278. Among these, the DNA fragment between +44 and +121 affects promoter activity more dramatically (about 6-7 fold). This DNA fragment contains the consensus promoter element previously reported to be important for photoreceptor cell-specific expression, and this promoter element seems to be working in the norpA gene expression (Doh, 1997).

Enzymatic activity of NorpA

To examine whether the norpA (no receptor potential A) gene encodes a phosphoinositide-specific phospholipase C (PLC) in the eye of Drosophila, a major PLC in an extract from normal Drosophila heads, which is absent in an extract from norpA mutant heads, was isolated and purified and its partial amino acid sequences were determined. The purified enzyme was found to be homogeneous on sodium dodecyl sulfate-polyacrylamide gel electrophoresis. The molecular weight of the enzyme was estimated to be 98,000 by sodium dodecyl sulfate-polyacrylamide gel electrophoresis. The purified enzyme hydrolyzes both phosphatidylinositol (PI) and phosphatidylinositol 4,5-bisphosphate (PIP2). Interestingly, the calcium and pH requirements for activation of the crude enzyme (KCl extract) are quite different from those of partially purified enzyme. The maximal activity for PIP2 hydrolysis is observed at calcium concentrations between 10(-7) and 10(-5) M for both the crude and partially purified enzymes. In contrast, the activity for PI hydrolysis of the crude enzyme increases with increasing calcium concentrations, while that of the partially purified enzyme reaches a maximum at calcium concentrations between 10(-6) and 10(-4) M, and decreases at millimollar concentration. The pH dependences for PI hydrolysis of the crude enzyme and the partially purified enzyme are similar. The crude enzyme hydrolyzes PIP2 over a broad pH range from 6 to 8.5, while the activity of the partially purified enzyme monotonously increases with increasing pH. The partial amino acid sequences were determined by treating the purified enzyme with endopeptidase Lys-C; the resultant peptide fragments were purified on a high performance liquid chromatography-reverse phase column and then sequenced with sequencer. The obtained sequences were found to be a part of the deduced amino acid sequences of cDNA, which was suggested to be norpA gene (Toyoshima, 1990).

Fatty acid and InsP3 signaling downstream of NorpA

Light-sensitive channels encoded by the Drosophila transient receptor potential-like gene (trpl) are activated in situ by an unknown mechanism requiring activation of Gq and phospholipase C (PLC). Recent studies have variously concluded that heterologously expressed TRPL channels are activated by direct Gq-protein interaction, InsP3 or Ca2+. In an attempt to resolve this confusion an exploration was carried out of the mechanism for the activation of TRPL channels co-expressed with a PLC-specific muscarinic receptor in a Drosophila cell line (S2 cells). Simultaneous whole-cell recordings and ratiometric Indo-1 Ca2+ measurements indicate that agonist (CCh)-induced activation of TRPL channels is not always associated with a rise in Ca2+. Internal perfusion with BAPTA (10 mM) reduces, but does not block, the response to agonist. In most cases, releasing caged Ca2+ facilitates the level of spontaneous channel activity, but similar concentrations (200-500 nM) can also inhibit TRPL activity. Releasing caged InsP3 invariably releases Ca2+ from internal stores but has only a minor influence on TRPL activity and none at all when Ca2+ release is buffered with BAPTA. Caged InsP3 also fails to activate any light-sensitive channels in situ in Drosophila photoreceptors. Two phospholipase C inhibitors (U-73122 4 microM and bromo-phenacyl bromide 50 microM) reduce both spontaneous and agonist-induced TRPL activity in S2 cells. The results suggest that, as in situ, TRPL activation involves G-protein and PLC; that Ca2+ can both facilitate and in some cases inhibit TRPL channels, but that neither Ca2+ nor InsP3 is the primary activator of the channel (Hardie, 1998).

Phototransduction in invertebrate microvillar photoreceptors is thought to be mediated by the activation of phospholipase C (PLC), but how this leads to gating of the light-sensitive channels is unknown. Most attention has focused on inositol-1,4,5-trisphosphate, a second messenger produced by PLC from phosphatidylinositol-4,5-bisphosphate; however, PLC also generates diacylglycerol, a potential precursor for several polyunsaturated fatty acids, such as arachidonic acid and linolenic acid. Both of these fatty acids reversibly activate native light-sensitive channels [transient receptor potential (TRP) and TRP-like (TRPL)] in Drosophila photoreceptors as well as recombinant TRPL channels expressed in Drosophila S2 cells. Recombinant channels are activated rapidly in both whole-cell recordings and inside-out patches, with a half-maximal effector concentration for linolenic acid of approximately 10 microM. Four different lipoxygenase inhibitors, which might be expected to lead to build-up of endogenous fatty acids, also activate native TRP and TRPL channels in intact photoreceptors. Since arachidonic acid may not be found in Drosophila, it is suggested that another polyunsaturated fatty acid, such as linolenic acid, may be a messenger of excitation in Drosophila photoreceptors (Chyb, 1999).

Drosophila phototransduction is a G protein-coupled, calcium-regulated signaling cascade that serves as a model system for the dissection of phospholipase C (PLC) signaling in vivo. The Drosophila light-activated conductance is constituted in part by the Transient receptor potential (Trp) ion channel, yet trp mutants still display a robust response, which demonstrates the presence of additional channels. The transient receptor potential-like (trpl) gene encodes a protein displaying 40% amino acid identity with TRP. Mammalian homologs of TRP and TRPL recently have been isolated and postulated to encode components of the elusive I(crac) conductance. TRP and TRPL localize to the membrane of the transducing organelle, together with rhodopsin and PLC, consistent with a role in PLC signaling during phototransduction. To determine the function of TRPL in vivo, trpl mutants were isolated and characterized physiologically and genetically. The light-activated conductance is composed of TRP and TRPL ion channels and each can be activated on its own. Genetic and electrophysiological tools were used to study the contribution of each channel type to the light response and show that TRP and TRPL can serve partially overlapping functions (Niemeyer, 1996).

Membrane association of NorpA

Severe mutations within the norpA gene of Drosophila abolish the photoreceptor potential and render the fly blind by deleting phospholipase C, an essential component of the phototransduction pathway. The predominant measurable phospholipase C activity in head homogenates has been shown to be encoded by norpA. Biochemical assays as well as antisera generated against the major gene product of norpA were used to examine PLC subcellular distribution before and during phototransduction. Both phospholipase C activity and the NorpA protein are predominantly associated with membrane fractions in heads of both light- and dark-adapted flies. Moreover, phospholipase C activity as well as NorpA protein can be easily extracted from membrane preparations of light- or dark-adapted flies using high salt, indicating that the NorpA protein is peripherally localized on the membrane. These data suggest that the norpA encoded phospholipase C of Drosophila is a permanent peripheral membrane protein. If this is indeed the case, then it would mean that the reversible redistribution of phospholipase C from the cytosol to the membrane, as observed in epidermal growth factor receptor stimulation of mammalian phospholipase C gamma, is not a universal mechanism utilized by all types of phosphatidylinositol-specific phospholipase C (McKay, 1994b).

Ca2+ and the phosphoinositide pathway

Photoreceptors of dissociated Drosophila retinae were loaded with the fluorescent Ca2+ indicators, fluo-3 and Calcium Green-5N. In fluo-3-loaded, wild-type photoreceptors, a rapid increase in fluorescence (Ca2+ signal) accompanies the light-evoked inward current. Removal of extracellular Ca2+ greatly reduces the Ca2+ signal, indicating Ca2+ influx as its major cause. In Calcium Green-5N-loaded trp mutants, which lack a large fraction of the Ca2+ permeability underlying the light-evoked inward current, the Ca2+ signal is smaller relative to wild-type photoreceptors. Fluo-3-loaded norpA mutant photoreceptors, which lack a light-activated phospholipase C, generate no light-evoked inward current and no Ca2+ signal. The phosphoinositide pathway therefore appears necessary for both excitation and changes in cytosolic free Ca2+ concentration (Peretz, 1994).

Light stimulates phosphatidylinositol bisphosphate phospholipase C (PLC) activity in Drosophila photoreceptors. The mechanism of this reaction was investigated by assaying PLC activity in Drosophila head membranes using exogenous phospholipid substrates. PLC activation depends on the photoconversion of rhodopsin to metarhodopsin and is reduced in norpAEE5 PLC and ninaEP332 rhodopsin mutants. NorpA PLC is stimulated by light at free Ca2+ concentrations between 10 nM and 1 microM. This finding is consistent with a Ca(2+)-mediated positive feedback mechanism that contributes to the rapid temporal response of invertebrate photoreceptor cells. The guanyl nucleotide dependence of light-stimulated PLC activity indicates that a G protein regulates NorpA. This was confirmed by the observation that light stimulation of PLC activity is deficient in mutants that lack the eye-specific G protein beta subunit G beta e. These results indicate that G beta e functions as the beta subunit of the G protein coupling rhodopsin to NorpA PLC (Running Deer, 1995).

Drosophila phototransduction is a phosphoinositide-mediated and Ca(2+)-regulated signaling cascade ideal for the dissection of feedback regulatory mechanisms. To study the roles of intracellular Ca2+ ([Ca2+]i) in this process, novel techniques were developed for the measurement of [Ca2+]i in intact photoreceptors. Flies were genetically engineered to express a UV-specific rhodopsin in place of the normal rhodopsin, so that long wavelength light can be used to image [Ca2+]i changes while minimally exciting the photoreceptor cells. Activation with UV generates [Ca2+]i increases that are spatially localized to the rhabdomeres and that are entirely dependent on the influx of extracellular Ca2+. Application of intracellular Ca2+ chelators of varying affinities demonstrates that the Ca2+ influx initially generates a large-amplitude transient that is crucial for negative regulation. Internal Ca2+ stores were revealed by discharging them with thapsigargin. But, in contrast to proposals that IP3-sensitive stores mediate phototransduction, thapsigargin does not mimic or acutely interfere with photoexcitation. Finally, a photoreceptor-specific PKC was identified as essential for normal kinetics of [Ca2+]i recovery (Ranganathan, 1994).

Disruption of phospholipase C-beta (PLC) by the norpA mutations of Drosophila renders flies blind by affecting the light-evoked photoreceptor potential. The norpA-coded PLC modulates the 1,4-dihydropyridine (DHP)-sensitive Ca2+ channels in larval muscles. The DHP-sensitive current is reduced in the norpA mutants. Application of 1 microM phorbol 12-myristate 13-acetate (TPA) and 1 microM phorbol 12,13-didecanoate (PDD), both activators of protein kinase C (PKC), rescues the current in the mutant fibers without significantly affecting the normal current. 4Alpha-phorbol 12,13-didecanoate (4alphaPDD), an inactive analog of PDD, does not affect either the normal or the mutant current. One micromolar bisindolylmaleimide (BIM), an inhibitor of PKC, reduces the current in the normal fibers without affecting the mutant current. 300 microM sn-1,2-dioctanoyl-glycerol (DOG), an analog of diacylglycerol (DAG), increases the current in the mutant fibers. These experiments suggest that the DHP-sensitive Ca2+ channels in Drosophila may be modulated by the PLC-DAG-PKC pathway, and that the same PLC isozyme, which is involved in phototransduction in the adult flies, may also modulate muscle Ca2+ channels in the larval stage of development (Gu, 1997).

The SOCS box protein STOPS is required for phototransduction through its effects on phospholipase C

Phosphoinositide-specific phospholipase C (PLC) isozymes play roles in a diversity of processes including Drosophila phototransduction. In fly photoreceptor cells, the PLCbeta encoded by norpA is critical for activation of TRP channels. This study describes a PLCbeta regulator, STOPS (slow termination of phototransduction), which encodes a SOCS box protein. Mutation of stops resulted in a reduced concentration of NORPA and a defect in stopping signaling following cessation of the light stimulus. NORPA has been proposed to have dual roles as a PLC- and GTPase-activating protein (GAP). The slow termination resulting from expressing low levels of wild-type NORPA was suppressed by addition of normal amounts of an altered NORPA, which had wild-type GAP activity, but no PLC activity. STOPS is the first protein identified that specifically regulates PLCbeta protein concentration. Moreover, this work demonstrates that a PLCbeta derivative that does not promote TRP channel activation, still contributes to signaling in vivo (Wang, 2008).

PLC isozymes play vital roles in signal transduction by cleaving the polar head group of phosphatidylinositol 4,5-bisphosphate (PIP2) to generate inositol-1,4,5-trisphosphate (IP3) and diacylglycerol (DAG). The most intensively studied PLC subtype, PLCβ, functions in signaling cascades initiated by stimulation of seven transmembrane domain G-protein coupling receptors (GPCRs). These GPCRs engage Gq, a member of the heterotrimeric GTP-binding protein family resulting in dissociation of the α and βγ subunits. One of these subunits then binds to and activates PLCβ, increasing its catalytic activity and thereby amplifying signaling (Wang, 2008).

In vitro analyses of mammalian PLCβ indicate that they also serve as GTPase activating proteins (GAPs), in addition to the more classical role in catalyzing the hydrolysis of PIP2. PLCβ1 increases the steady-state GTPase activity up to 20 fold, resulting in fast deactivation of Gq. Thus, the regulation of Gq through the GAP activity of PLCβs potentially forms a short negative feedback loop that contributes to high signal resolution. An open question is whether PLCβs function as GAPs in vivo (Wang, 2008).

The PLCβ required for Drosophila phototransduction has been suggested to be a dual functional protein, serving as a both a GAP and phospholipase C. Fly visual transduction is initiated by light activation of rhodopsin and engagement of the Gαq effector, which leads to stimulation of the PLCβ encoded by the norpA (no receptor potential A) locus. The cascade culminates with the opening of the TRP and TRPL cation channels (Wang, 2008).

Null mutations in norpA abolish the light response, while weak alleles display reduced light sensitivity, slow activation and decreased rates in the termination of the photoresponse. Weak norpA alleles express reduced levels of the NORPA protein, leading to the suggestion that the defect in termination results from a reduction in GAP activity. However, an alternative possibility is that the slow termination is a consequence of decreased PLC activity, since the activities of TRP and TRPL are dependent on hydrolysis of PIP2, and Ca2+ influx via the channels is required for rapid termination. Thus the basis for the slow termination associated with expression of low quantities of NORPA remains unresolved. Defects in termination of G protein signaling can lead to many deleterious consequences in mammals, such as cardiac dysfunction, decreased fertility, deficits in the immune system, altered sensory responses, including problems in adapting to abrupt changes in light levels, and cell death. Given the diverse expression patterns and roles of PLCβ, understanding the basis through which PLCβ expression impacts on response termination has broad implications (Wang, 2008).

The expression of different PLCβ isoforms at appropriate levels and in distinct cell types is potentially a mechanism of control that applies to both mammalian and Drosophila PLCβs. For example, the NORPA PLCβ is expressed primarily in the Drosophila retina, and the mammalian PLCβ2 which functions in leukocyte signaling, is highly expressed in cells of the immune system. However, the proteins that regulate the cell-type specific expression of PLC proteins are unknown (Wang, 2008).

The current study identified a mutation in an eye-enriched SOCS box protein, which has been named Slow Termination of Phototransduction (STOPS). Known SOCS box proteins bind to the elongin B/C complex and promote the ubiquitination and proteasomal degradation of target proteins (reviewed in Kile, 2002). In contrast to these other proteins, STOPS functions independently of elongin B and C and is essential for expression of maximal levels of NORPA. STOPS is also required for stopping signaling upon cessation of the light stimulus as a consequence of the reduced NORPA expression. The defective termination in the stops mutant was due to decreased GAP activity of NORPA rather than a reduction in PLC activity, thereby providing strong evidence that NORPA functions as a GAP in vivo. These data demonstrate a novel mode for controlling PLCβ expression in photoreceptor cells (Wang, 2008).

Many PLCβ isoforms, such as the NORPA protein, which functions in fly phototransduction, are expressed in distinct subsets of cells. The current demonstrates that NORPA expression in photoreceptor cells depends on the STOPS protein. Mutations in stops caused a decrease in NORPA protein concentration, resulting in slow termination of the photoresponse (Wang, 2008).

A correlation between low NORPA expression and slow response termination has been proposed previously since multiple norpA alleles as well as inaD2 express reduced concentrations of NORPA and display termination defects. However, these mutants have additional alterations, precluding the conclusion that low levels of NORPA prevent normal termination of the photoresponse. For example, hypomophic norpA mutants such as norpAP57 and norpAP16 express mutant rather than wild-type NORPA. Moreover, the interaction of NORPA with the INAD scaffold protein is disrupted in inaD2 and norpAC1094S, suggesting that the INAD-NORPA interaction contributes to the termination phenotype in these mutant flies (Wang, 2008).

This study provides two lines of evidence that a normal concentration of NORPA is essential for stopping signaling after cessation of the light stimulus. First, the stops mutant expresses decreased quantities of wild-type NORPA but not other proteins in photoreceptor cells, resulting in slow termination of the light response. Second, the amount of wild-type NORPA was manipulated using the heat shock promoter. The results showed a strong relationship between the termination rate and the concentration of NORPA protein (Wang, 2008).

A question concerns the mechanism through which reduced amounts of NORPA cause a termination defect. In principle, the slow termination could result from a combination of low NORPA levels, and a decrease in intrinsic enzyme activity, due to a requirement for STOPS as a cofactor. However, this does not appear to be the case as the termination defect is indistinguishable between stops+ flies that express the same low levels of NORPA (expressed under the control of the hsp70 promoter in a norpA mutant background) as is produced in stops1 flies. STOPS does not co-immunoprecipitate with the TRP channels, suggesting that it does not cause defects in termination through direct interactions with the TRP channel. Moreover, the ERG response is the same in trpP343 and trpP343, stops1 flies, suggesting that STOPS does not alter the activity of the TRPL channel. Furthermore, STOPS does not co-immunoprecipitate with the scaffold protein, INAD, or alter the concentration of any known member of the signalplex other than NORPA, indicating that the termination phenotype in stops1 does not result from destabilization of the signalplex (Wang, 2008).

In addition to serving as a phospholipase C, mammalian PLCβs and NORPA have been proposed to be GAPs. Therefore, according to one model, low NORPA levels cause a termination defect by decreasing GAP activity, thereby leading to sustained activity of the Gαq following light stimulation. However, previous work did not exclude that the slow termination resulting from a reduced NORPA concentration was due to a requirement for PLC activity. Thus, an alternative possibility is that the slow termination is a consequence of decreased light-dependent Ca2+ influx, since the NORPA phospholipase C activity leads to opening of the TRP and TRPL channels. A rise in Ca2+ is important for termination, as the rate is decreased in flies overexpressing the Na+/Ca2+ exchanger, CalX, or if the photoreceptor cells are illuminated in a Ca2+-free bath (Wang, 2008).

The results indicate that the slow termination due to a low concentration of NORPA is caused by reduced GAP activity rather than diminished intracellular Ca2+. In support of this conclusion, the delayed termination was not suppressed by a mutation in calx, which eliminates Ca2+ extrusion. Rather, it was found that slow termination of the photoresponse was fully reversed by expression of a PLC-derivative, NORPAS559A, which contains a mutation in a residue critical for activation of the photoresponse. Since NORPAS559A fully retained GAP activity, these data indicate that the GAP activity of NORPA is essential for arresting signaling following cessation of the light stimulus. The observation that introduction of normal levels of NORPAS559A, suppresses the termination defect resulting from expression of a low concentration of wild-type NORPA, indicates that more than one NORPA molecule can interact successively with the same activated Gαq. This proposal is consistent with the evidence that NORPA forms a homodimer. In addition, it appears that a single activated Gαq-GTP is capable of interacting sequentially with multiple independent NORPA molecules (Wang, 2008).

Following activation, rapid termination of the light response is essential for high temporal resolution to ensure appropriate responses to subsequent stimuli. Since G-protein deactivation appears to be the rate-limiting step for termination in mammalian phototransduction cascade, timely deactivation of G-protein may be equally important for regulation of Drosophila phototransduction. Given that NORPA is the direct target for the G-protein, stimulation of the GTPase activity of the Gαq represents a highly efficient and rapid mode of negative feedback regulation (Wang, 2008).

The current work has demonstrated that the SOCS box protein, STOPS, is required specifically for expression of NORPA in photoreceptor cells. SOCS proteins were initially identified as suppressors of cytokine signaling and contain a common C-terminal 40 amino acid SOCS box. Genomic analyses led to the identification of many additional SOCS box-containing proteins, which are subdivided into groups based on their diverse N-terminal domains. Examples include an SH2 domain (SOCS), WD40-repeats (WSB), a SPRY-domain (SSBs), a RAB domain (RAR), a domain conserved in the Neuralized family of proteins (Neuralized-like) and ankyrin-repeats (ASBs). Among the mammalian proteins, STOPS is most similar to the human CRA-b isoform of ASB15, since STOPS and CRA-b share additional homology (STOPS domain) that extends N-terminal to the SOCS box (Wang, 2008).

Current understanding about SOCS box containing proteins is that they function as adaptor molecules for the E3 ubiquitin ligase complex to target signaling proteins to the protein degradation pathway (Kile, 2002). The variable N-terminal domain interacts with target proteins thereby defining the substrate specificity for the E3 ubiquitin ligase complex. The SOCS box binds to a heterodimer composed of ubiquitin-like elongin B and Skp1-like elongin C, and forms an E3 ubiquitin ligase complex with Cullin-2 and Rbx-1. In C. elegans, the ZIF SOCS box protein functions in the exclusion of germ-line proteins from somatic lineages by interacting with the elongin B/C complex and targeting the somatic CCCH finger protein for degradation in a cullin and Rbx-dependent manner (Wang, 2008).

In contrast to all other characterized SOCS box proteins, which function in protein degradation, STOPS has an opposite role in promoting expression of NORPA in photoreceptor cells. Consistent with this observation, the elongin B/C pathway was not required for expression of NORPA. The elongin-B and elongin-C mutants expressed normal amounts of NORPA and displayed wild-type light responses. Thus, as expected the elongin B/C complex does not function as a positive regulator of NORPA. Furthermore, a double elongin-B, stops1 mutant displayed the same decreased NORPA concentration and termination defect as the single stops1 mutant, indicating that the elongin B/C complex does not function in a pathway opposing STOPS. Nevertheless, mutations in the SOCS box disrupt STOPS function. Taken together, these data indicate that although STOPS is dependent on the SOCS box, it acts independently of the elongin B/C complex in vivo. Thus, STOPS is distinct from previously characterized SOCS box proteins (Wang, 2008).

The expression patterns of many signaling proteins are restricted to ensure that they function in a cell-type specific manner. In wild-type flies, NORPA is expressed predominately in photoreceptor cells, but is still detected in other tissues. It was found that the STOPS protein is required for expression of NORPA only in photoreceptor cells since in the stops1 retina, NORPA is reduced by >90% without affecting NORPA in other tissues. In hs-norpA flies, which expressed NORPA under the control of heat-shock promoter, the NORPA protein was expressed primarily in the head but not in the body, although the mRNAs were present in both the head and body. Moreover, in the head of hs-norpA flies, NORPA protein was enriched in the retina (Wang, 2008).

Although STOPS is required for relatively high expression of NORPA, it is not sufficient. In heat-shocked norpAP24;hs-stops;hs-norpA flies, which expressed both the stops and norpA RNAs broadly, NORPA was still expressed principally in the retina. In HEK293T cells, coexpression of STOPS with NORPA did not result in an elevation of NORPA levels beyond that obtained in cells expressing NORPA alone. Moreover, NORPA and STOPS did not co-immunoprecipitate either in fly heads or after expressing the two proteins in HEK293T cells. Thus, there appear to be one or more additional factors that remain to be identified that function in concert with STOPS to promote NORPA expression. Finally, the current work describes a novel mode for controlling the expression of a PLCβ and raises the possibility that there exist mammalian SOCS box proteins that function independently of the elongin B/C complex to promote the expression of PLCβ and other signaling proteins in distinct subsets of cells (Wang, 2008).

Function of rhodopsin in temperature discrimination in Drosophila

Many animals, including the fruit fly, are sensitive to small differences in ambient temperature. The ability of Drosophila larvae to choose their ideal temperature (18°C) over other comfortable temperatures (19° to 24°C) depends on a thermosensory signaling pathway that includes a heterotrimeric guanine nucleotide-binding protein (G protein), a phospholipase C, and the transient receptor potential TRPA1 channel. Mutation of the gene (ninaE) encoding a classical G protein-coupled receptor (GPCR), Drosophila rhodopsin, eliminates thermotactic discrimination in the comfortable temperature range. This role for rhodopsin in thermotaxis toward 18°C was light-independent. Introduction of mouse melanopsin restored normal thermotactic behavior in ninaE mutant larvae. It is proposed that rhodopsins represent a class of evolutionarily conserved GPCRs that are required for initiating thermosensory signaling cascades (Shen, 2011).

Temperature sensation in animals is mediated largely by direct activation of transient receptor potential (TRP) ion channels. An exception is a TRP channel in Drosophila larvae that functions indirectly in the selection of their optimal temperature (18°C) over other comfortable temperatures (19° to 24°C) and does so through a signaling cascade that includes a heterotrimeric guanine nucleotide-binding protein (G protein) Gq, phospholipase C (PLC), and the TRPA1 channel. A thermosensory signaling cascade is also required in Caenorhabditis elegans, which includes guanylate cyclases and a guanosine 3',5'-monophosphate (cGMP)-gated channel. Thermosensory signaling cascades may contribute to amplification of small temperature differences and to adaptation to temperatures that are less than optimal, but still permissive for survival (Shen, 2011).

G protein-coupled receptors (GPCRs) are candidates to initiate thermosensory cascades because they couple to pathways that include Gq, PLC, and TRP channels, as well as to cascades that engage guanylate cyclases and cGMP-gated channels. However, there are up to 200 hundred GPCRs encoded in flies and over one thousand in worms, and there is no precedent for a GPCR that functions in thermosensation (Shen, 2011).

It was of interest to find out whether the canonical GPCR (rhodopsin) might be required for thermosensation, even though it is thought to function exclusively in light sensation. The basis for this proposal is that the same Gq (Gα49B) and PLC [No Receptor Potential A (NORPA)] that function in light sensation and link rhodopsin to activation of TRP channels are required for larvae to move preferentially toward the 18°C region when the alternative zone is held at another temperature in the 19° to 24°C range). If this behavior requires rhodopsin, it would be a light-independent function, because thermotaxis takes place effectively in the dark (Shen, 2011 and references therein).

To test temperature selection, larvae were placed on a plate between two temperature zones, one of which was kept at 18°C and the other at an alternative temperature. After 10 min, the larvae in each zone were counted and the preference index (PI) was calculated. A lack of temperature bias results in a PI of 0, whereas a complete preference for 18°C or the alternative temperature results in a PI of 1.0 or -1.0, respectively. Wild-type larvae select 18°C over any other temperature, including other temperatures in their comfortable range (20° to 24°C) (Shen, 2011).

To address whether the major opsin (Rh1) encoded by the ninaE gene was required for thermotaxis in their comfortable temperature range, flies were tested with a deletion that removed the ninaE coding region (ninaEI17). The ability to distinguish 18° from 24°C was impaired in ninaEI17 larvae and in animals containing the ninaEI17 mutation in trans with another deletion (Df) that removed ninaE on the homologous chromosome. This phenotype was indistinguishable from the thermotaxis deficits resulting from mutations disrupting PLC (norpAP24) or the TRPA1 channel (trpA11). Flies with any of five of six additional ninaE alleles showed deficits in discrimination between 18° and 24°C, but not between 18°C and cooler or very warm temperatures. Larvae with one missense allele, ninaEP332, strongly preferred 18°C over 24°C, although the bias for 18°C was eliminated when the alternative temperature was either 20° or 22°C (Shen, 2011).

To confirm that the thermotaxis defect was due to mutation of ninaE, tests were performed for rescue of the phenotype with a wild-type transgene, using the GAL4-UAS system. This approach employs the yeast GAL4 transcription factor that binds to the upstream activation sequence (UAS) to promote transcription. Only ninaE17 larvae containing both the ninaE-GAL4 and UAS-ninaE transgenes effectively chose 18°C over 24°C. Another GPCR (serotonin receptor; UAS-5-HT2), which is most similar to mammalian Gq-coupled serotonin receptors, does not rescue the ninaEI17 deficit. Similar to the norpAP24 and trpA11 phenotypes, loss of ninaE impaired discrimination between 18°C and other temperatures in the comfortable range, 20° or 22°C, but not selection of 18°C over cooler (14° or 16°C) or warmer temperatures (26° to 32°C) (Shen, 2011).

In Drosophila, the vitamin A-derived chromophore stably binds to the opsin and is required for Rh1 to exit the endoplasmic reticulum. Wild-type larvae grown on food depleted of vitamin A, or mutant larvae (santa maria1) missing a scavenger receptor required for chromophore generation, showed impaired temperature discrimination in the 18°C to 24°C range. The defect in santa maria1 was reversed by adding all trans-retinal to the food (Shen, 2011). To address whether Rh1 might function in the same cells as other components involved in 18° to 24°C thermotaxis, UAS-RNAi transgenes were expressed under the transcriptional control of the ninaE-GAL4 or the trpA1-GAL4. Expression of Gα49B, norpA, or trpA1 RNA interference (RNAi) transgenes using the ninaE-GAL4 reduced the biases toward 18°C over 22° or 23°C. Similarly, the preference for 18°C was diminished in larvae expressing the ninaE RNAi under control of the trpA1-GAL4. Expression of UAS-ninaE+ under control of the trpA1-GAL4 restored 18° versus 24°C temperature discrimination in ninaEI17 larvae (Shen, 2011).

Because rhodopsin is a light sensor, whether thermotactic behavior is altered by light was tested. Wild-type larvae chose 18° over 24°C equally well in the light or dark. Moreover, ninaEI17 displayed similar thermotactic impairments in the presence or absence of light. Thus, selection of 18° over 24°C was light-independent (Shen, 2011).

Larvae that were unresponsive to light were also tested. Wild-type early third instar larvae avoid white or blue, but not orange, light. For larvae given a choice between 18° and 23°C, the aversion to light overcame the preference for 18°C. Bolwig’s organs, which consist of larval photoreceptor cells that function in the avoidance of moderate light intensities, do not express the trpA1-GAL4. norpAP24 animals are not negatively phototactic, and expression of UAS-norpA, under the control the trpA1-GAL4 does not restore negative phototaxis. These larvae discriminated temperatures in the 18° to 23°C range, and this behavior was not affected by light (Shen, 2011).

The ninaE gene appeared to be expressed at an exceptionally low level because no signal was detected in larvae with Rh1 antibodies or using the ninaE-GAL4 to drive UAS-GFP. Low amounts of Rh1 might prevent efficient light activation of Rh1 in thermosensory neurons, which might impair thermotactic discrimination. To provide additional evidence that ninaE was coexpressed with trpA1, neurons were dissected from the body wall and the anterior region that expressed the trpA1-reporter (trpA1-GAL4 and UAS-mCD8-GFP; mCD8 is the mouse CD8 receptor), and reverse transcription polymerase chain reaction (RT-PCR) was performed. ninaE RT-PCR products were detected in 5 out of 15 green fluorescent protein (GFP)-positive neurons (3 out of 8 from the body wall; 2 out of 7, anterior region), but not in any dissected GFP negative neurons (Shen, 2011).

Selection of 17.5° to 18°C over cooler temperatures occurs through avoidance that results from increased turning at slightly lower temperatures. To test whether the preference for 18° over slightly higher temperatures occurred through a similar mechanism, larvae were tracked. Wild-type larvae appeared to progress only a short distance into the 24°C area before they paused, stretched their heads, and initiated their first turns. However, ninaEI17, norpAP24, and trpA11 mutant larvae did not appear to turn until they traversed far into the 24°C zone (Shen, 2011).

To quantify turning behavior, a simple assay was developed. The 24°C zone was demarcated with 20 lines, the larvae were released on the 18°C side near the 24°C interface, and the last line crossed before the larvae made their first turn was tabulated. Larvae were only counted that moved perpendicular to the lines (~5° deviation). Wild-type larvae turned near line 3. However, the mutant larvae traveled to near line 14 in the 24°C area before turning. The much greater distances traveled by the mutants before turning did not appear to be due to increased movement speeds, because all the larvae moved at similar rates. In a reciprocal experiment, larvae were placed on the 24°C side, and animals were monitored that crossed perpendicular to the lines demarcating the 18°C zone. Wild-type larvae did not turn until line 10, and there were only small variations between wild-type and mutant animals (Shen, 2011).

Tests were performed to see whether the higher rate of larval turning at 24°C was dependent on prior exposure to a lower temperature. Wild-type larvae placed on a plate uniformly held at a single temperature showed similar turning frequencies at all temperatures tested (18° to 24°C). Similar results were obtained with the ninaEI17, norpAP24, and trpA11 larvae. Thus, turning at 24°C was dependent on prior exposure to 18°C (Shen, 2011).

Several results argue strongly against a developmental defect underlying the thermotaxis impairment in the comfortable range. First, although ninaEP332 larvae were impaired in selecting 18°C over 20° or 22°C, they were able to choose 18°C over 24°C. Second, multiple ninaE missense mutations, including ninaEP332 and ninaEP318, have no apparent effects on morphogenesis and are not associated with retinal degeneration, which suggests that these alleles do not affect development of the thermosensory neurons. Third, indistinguishable numbers and morphological appearances of GFP-positive cells were found in wild-type and ninaEI17 larvae that expressed UAS-mCD8-GFP under control of the trpA1-GAL4 (Shen, 2011).

Advantage was taken of the slightly higher PI exhibited by ninaEP332 (18° versus 24°C) to test whether other genes required for thermotaxis functioned subsequent to ninaE. Introduction of the Gα49B1, norpAP24 or trpA11 mutations into the ninaEP332 background prevented 18°C selection over 24°C. Another mutation that causes a higher-than-normal PI disrupts the rhodopsin phosphatase (rdgC306). The combination of ninaEI17 or Gα49B1 with rdgC306 eliminated the bias for 18° over 24°C. These analyses indicate that Gq, PLC, and TRPA1 function in a pathway downstream of Rh1 (Shen, 2011).

Drosophila encodes additional opsins (Rh2-6). To determine whether other opsins could substitute for Rh1, Rh2-6 were expressed under control of the ninaE promoter in ninaEI17 flies, and 18° versus 24°C selection was assayed. With the exception of Rh3, other opsins could replace Rh1. However, the transgenic flies showed significant differences from wild type when given a choice between 18° and 20° to 22°C. Another GPCR coupled to Gq [5-hydroxytryptamine (5-HT2)] did not function in place of Rh1 (Shen, 2011).

The mammalian opsin that is most similar to Drosophila Rh1 is melanopsin (OPN4). Expression of Opn4 under control of the ninaE promoter did not reverse the phototransduction defect in adult ninaEI17. However, Opn4 enabled the ninaEI17 larvae to distinguish between 18°C and 24°C (Shen, 2011).

The observations that Rh1 is required for thermosensory discrimination and that OPN4 could substitute for Rh1 suggest that Rh1 and related opsins might be intrinsic thermosensors. However, the intrinsic rate of thermal activation, which is ~1/min in fly photoreceptor cells, is far too low to account for the requirement for Rh1 for thermosensation. It is suggested that an accessory factor might interact with Rh1 and accelerates its intrinsic thermal activity. Finally, because rhodopsin has dual roles, it is interesting to consider the question as to whether the archetypal role for rhodopsin was in light sensation or in thermosensation (Shen, 2011).

Functional cooperation between the IP3 receptor and Phospholipase C secures the high sensitivity to light of Drosophila photoreceptors in vivo

Drosophila phototransduction is a model system for the ubiquitous phosphoinositide signaling. In complete darkness, spontaneous unitary current events (dark bumps) are produced by spontaneous single Gqα activation, while single-photon responses (quantum bumps) arise from synchronous activation of several Gqα molecules. Recent studies have shown that most of the spontaneous single Gqα activations do not produce dark bumps, because of a critical phospholipase Cβ (PLCβ) activity level required for bump generation. Surpassing the threshold of channel activation depends on both PLC activity and cellular [Ca(2+)], which participates in light excitation via a still unclear mechanism. This study shows that in IP3 receptor (IP3R)-deficient photoreceptors, both light-activated Ca(2+) release from internal stores and light sensitivity were strongly attenuated. This was further verified by Ca(2+) store depletion, linking Ca(2+) release to light excitation. In IP3R-deficient photoreceptors, dark bumps were virtually absent and the quantum-bump rate was reduced, indicating that Ca(2+) release from internal stores is necessary to reach the critical level of PLCβ catalytic activity and the cellular [Ca(2+)] required for excitation. Combination of IP3R knockdown with reduced PLCbeta catalytic activity resulted in highly suppressed light responses that were partially rescued by cellular Ca(2+) elevation, showing a functional cooperation between IP3R and PLCβ via released Ca(2+). These findings suggest that in contrast to the current dogma that Ca(2+) release via IP3R does not participate in light excitation, this study shows that released Ca(2+) plays a critical role in light excitation. The positive feedback between PLCβ and IP3R found here may represent a common feature of the inositol-lipid signaling (Kohn, 2015).

In this study, in vivo light-response suppression was accompanied by reduced Ca2+ release from IP3-sensitive stores. In addition, the rate of spontaneously produced dark bumps, which is highly sensitive to Gqα-dependent PLCβ catalytic activity and cellular Ca2+ level, was virtually abolished in IP3R-deficient photoreceptors. This dark-bump elimination indicates that the suppressed Ca2+ release from IP3-sensitive stores underlies the suppressed catalytic activity of PLCβ, leading to suppressed light response in IP3R-deficient photoreceptors. Further evidence that the suppressed light response arises from inhibition of Ca2+ release from IP3-sensitive stores came from blocking the Ca2+ pump by Tg, which mimicked the phenotype of the IP3R-deficient photoreceptors in WT flies. The above findings indicate that IP3R-mediated Ca2+ release has a critical role in light excitation of Drosophila photoreceptors. The combination of the PLCβ mutant norpAH43 with IP3R-deficient photoreceptors, which synergistically suppressed the light response, strongly suggests that there is functional cooperation between the IP3R and PLCβ in generation of the light response (Kohn, 2015).

It has been previously shown that an increase in cytosolic Ca2+ participates in light excitation as evidenced by enhancement of the light response following photo release of caged Ca2+ at the rising phase of the light response. The target of Ca2+ action has not been entirely resolved. PLCβ is an important target for Ca2+ action and the regulation of its catalytic activity by Ca2+ has been thoroughly investigated. These studies showed that the positive charge of Ca2+ is used to counterbalance local negative charges formed in the active site during the course of the catalytic reaction. Accordingly, Ca2+ performs electrostatic stabilization of both the substrate and the transition state, thus providing a twofold contribution to lower the activation energy of the enzyme reaction (Kohn, 2015).

The following model explains how functional cooperation between the IP3R and PLCβ via the released Ca2+ operates and secures quantum-bump production: absorption of a single photon, which induces activation of several PLCβ molecules, is initially insufficient at resting Ca2+ levels to reach the critical level of PLCβ activity required for TRP/TRPL channel activation. Nevertheless, the IP3 molecules produced by the given PLCβ activity are able to activate the nearby IP3Rs, mobilize Ca2+ from the stores, and elevate PLCβ activity above the threshold required for TRP/TRPL channel activation. In addition, the released Ca2+ may also reduce the threshold of TRP/TRPL channel activation and allow bump generation. According to this model, the following enzymatic reactions may explain the current findings. Each Gqα-activated PLCβ has low catalytic activity due to the relatively low (<160 nM) resting Ca2+ concentration in the cytosol. In addition, each activated PLCβ remains active for only a short (approximately several tens of milliseconds) time due to the GTPase-activating protein activity of PLCβ that causes a rapid hydrolysis of Gqα-GTP followed by inactivation of PLCβ. The initial low catalytic activity of PLCβ is apparently below the threshold required for activation of the TRP and TRPL channels, but this low activity still results in hydrolysis of PIP2 producing IP3. Since there are no IP3 buffers in the microvilli and the IP3 degradation time is relatively slow (~1 s), the produced IP3 molecules diffuse fast along the microvillus at an estimated time of ~1 ms along 1 microm long microvillus and bind to IP3R located at the nearby submicrovillar cisternae (SMC; the photoreceptors' extensions of smooth ER). IP3R channels residing at the SMC, which are large channels with high sensitivity for IP3 and thus can be activated at low PLCβ activity, open and release Ca2+ juxtaposed to the base of the microvillus. The released Ca2+ steeply raises the local Ca2+ concentration, probably to the microM range, because of the very small aqueous volume of the microvillus and the relatively large local Ca2+ elevation via the release mechanism (Kohn, 2015).

Accordingly, a single IP3R channel can release ∼104 Ca2+ ions in 1 ms channel opening and Ca2+-induced Ca2+ release mechanism is a property of the IP3R channels and of the ryanodine receptors, which reside in the ER. Ca2+ released via IP3R of the WT SMC diffuse back toward the activated PLCβ and the TRP/TRPL channels in the microvillus. Although Ca2+ diffuses ∼20-fold slower than IP3 due to strong buffering, the diffusion constant strongly depends on Ca2+ concentration. Accordingly, at ~250 μM the Ca2+ diffusion coefficient is as large as that of IP3. Once a single TRP channel is activated, the large Ca2+ influx through this channel is sufficient to facilitate the rest of the active PLCβ molecules or reduce the threshold for TRP/TRPL channel activation in this microvillus and produce a bump that reflects activation of the entire microvillus . When there is abnormally low Ca2+ release via the IP3R because of low IP3R expression levels (IP3R-RNAi), there is not enough Ca2+ to increase PLC activity or to reduce TRP activation threshold, and activated PLC in this microvillus does not produce a bump, leading to abnormally low frequency of dark bumps (Kohn, 2015).

The invasive whole-cell recording technique, which was used in previous studies and avoided Ca2+ buffering of the pipette solution, most likely resulted in abnormally elevated cytosolic Ca2+ concentration, which also allowed the Ca2+ pump to keep the stores full. This artificially elevated cytosolic [Ca2+] together with the constitutive Ca2+ leak from the full stores, bypassed the need to mobilize Ca2+ via functional IP3R to facilitate PLCβ activity and reach its critical catalytic activity level needed to activate the TRP/TRPL channels. In the present study in the intact eye, a significant reduction in light-response amplitude was observed when the IP3R level was reduced. Furthermore, when cellular [Ca2+] was reduced by prolonged extracellular EGTA application, the light response of the IP3R-deficient flies was further suppressed. Moreover, when using invasive patch-clamp whole-cell recordings without Ca2+ buffering of the pipette solution, no significant difference between WT and IP3R-deficient flies was observed, as found in the previous study. However, when pipette Ca2+ was reduced with EGTA, the phenotype of reduced light excitation was observed in both reduced quantum-bump frequency as well as in macroscopic light-response suppression. Unlike quantum bumps, dark bumps were virtually eliminated even without buffering the pipette Ca2+ in IP3R-deficient flies, indicating that in the dark the IP3R-deficiency led to abnormally low cytosolic [Ca2+], possibly due to reduced Ca2+ leak from stores leading to cellular [Ca2+] below the critical level required for PLC activation observed in WT flies. Alternatively, the positive feedback between the released Ca2+ and PLC may function at single PLC molecules. Hence the nominal pipette Ca2+ is not sufficient to allow PLC activity to pass the threshold of channel activation, but the released Ca2+ via IP3R activation together with pipette Ca2+ allows PLC activity to pass this threshold and generate dark-bump (Kohn, 2015).

There is a striking functional similarity between, the cerebellar Purkinje cell (PC) proteins of the IP signaling and Drosophila photoreceptors, but the link of cerebellar mGluR1 receptor to TRPC3 activation is not clear. Interestingly, in PC neurons, stromal interaction molecule 1 (STIM1) was proved an essential regulator of Ca2+ level in neuronal endoplasmic reticulum Ca2+ stores. Accordingly, STIM1-specific deletion caused impairments in slow synaptic current and cerebellar motor behavior. Strikingly, refilling empty Ca2+ stores through increased Ca2+ level in the cytosol partially rescued the phenotype of the stim1 knock-out mice, reminiscent of the rescue of the phenotype of the IP3R-deficient fly by artificially elevated cytosolic Ca2+. Thus, the facilitatory role of released Ca2+ on PLC in light excitation of Drosophila photoreceptors represents an essential mechanism that operates in other PI systems (Kohn, 2015).

Protein Interactions

Interaction of NorpA with G protein alpha49B

The roles of the Drosophila Gq alpha proteins (DGq) were examined in the phototransduction pathway. The DGq proteins immunolocalize to the ocelli and all eight retinular photoreceptor cell rhabdomeres. An affinity-purified anti-DGq alpha immunoglobulin blocks the light-dependent GTP hydrolysis activity associated with Drosophila head membranes in vitro, suggesting that rhodopsin stimulates DGq. Dominantly active DGq1 mutants exhibit a light-independent GTPase activity and abnormal electrophysiological light responses, such as reduced retinal sensitivity and slow response kinetics, as compared with wild-type flies. Dominant DGq2 mutants exhibit a light-independent GTPase activity with normal electrophysiological light responses. Retinas of double mutants of DGq1, but not DGq2, with the light-dependent retinal degeneration mutant rdgB degenerate even in the dark. DGq1 stimulation of rdgB retinal degeneration in the dark is norpA-dependent. These results indicate that DGq1 mediates the stimulation by light-activated rhodopsin of the norpA-encoded phospholipase C in the visual transduction cascade (Y. J. Lee, 1994).

Heterotrimeric G proteins mediate a variety of signaling processes by coupling seven-transmembrane receptors to intracellular effector molecules. The Drosophila phototransduction cascade is a G protein-coupled signaling cascade that utilizes a phospholipase C (PLC beta) effector. PLC beta has been shown to be activated by Gq alpha in reconstituted systems. To determine whether a Gq-like protein couples rhodopsin to PLC, and to study its function, a mutant defective in a photoreceptor-specific Gq protein, DGq, was isolated. Gq is demonstrated to be essential for the activation of the phototransduction cascade in vivo. Transgenic flies were generated expressing DGq under an inducible promoter and it is possible to manipulate the sensitivity of a photoreceptor cell by controlled expression of DGq. Characterization of quantum bumps in mutants expressing less that 1% of the levels of DGq reveals that the rhodopsin-G protein interaction does not determine the gain of the single photon responses. Together, these results provide significant insight into the role of Gq in regulating the output of a photoreceptor cell (Scott, 1995).

Interaction of NorpA with Inad

The transient receptor potential protein (Trp) is a putative capacitative Ca2+ entry channel present in fly photoreceptors, which use the inositol 1,4,5-trisphosphate (InsP3) signaling pathway for phototransduction. By immunoprecipitation studies, Trp is found associated into a multiprotein complex with the norpA-encoded phospholipase C; an eye-specific protein kinase C (InaC), and with the InaD protein (InaD). InaD is a putative substrate of InaC and contains two PDZ repeats, putative protein-protein interaction domains. These proteins are present in the photoreceptor membrane at about equimolar ratios. The Trp homolog can be isolated together with NorpA, InaC and InaD from blowfly (Calliphora) photoreceptors. Compared to Drosophila Trp, the Calliphora Trp homolog displays 77% amino acid identity. The highest sequence conservation is found in the region that contains the putative transmembrane domains S1-S6 (91% amino acid identity). As investigated by immunogold labeling with specific antibodies directed against Trp and InaD, the Trp signaling complex is located in the microvillar membranes of the photoreceptor cells. The spatial distribution of the signaling complex argues against a direct conformational coupling of Trp to an InsP3 receptor supposed to be present in the membrane of internal photoreceptor Ca2+ stores. It is suggested that the organization of signal transducing proteins into a multiprotein complex provides the structural basis for an efficient and fast activation and regulation of Ca2+ entry through the Trp channel (Huber, 1996b).

Photoreceptors that use a phospholipase C-mediated signal transduction cascade harbor a signaling complex in which the phospholipase Cbeta (PLCbeta), the light-activated Ca2+ channel TRP, and an eye-specific protein kinase C (ePKC) are clustered by the PDZ domain protein InaD. The function of ePKC was investigated in three ways: by cloning the Calliphora homolog of Drosophila ePKC; by precipitating the TRP signaling complex with anti-ePKC antibodies, and by performing phosphorylation assays in isolated signaling complexes and in intact photoreceptor cells. The deduced amino acid sequence of Calliphora ePKC comprises 685 amino acids and displays 80.4% sequence identity with Drosophila ePKC. Immunoprecipitations with anti-ePKC antibodies leads to the coprecipitation of PLCbeta, TRP, InaD and ePKC but not of rhodopsin. Phorbolester- and Ca2+-dependent protein phosphorylation reveals that, apart from the PDZ domain protein InaD, the Ca2+ channel TRP is a substrate of ePKC. TRP becomes phosphorylated in isolated signaling complexes. TRP phosphorylation in intact photoreceptor cells requires the presence of extracellular Ca2+ in micromolar concentrations. It is proposed that ePKC-mediated phosphorylation of TRP is part of a negative feedback loop that regulates Ca2+ influx through the TRP channel (Huber, 1998).

Drosophila InaD, which contains five tandem protein interaction PDZ domains, plays an important role in the G protein-coupled visual signal transduction. Mutations in inaD alleles display mislocalizations of signaling molecules of phototransduction that include the essential effector, phospholipase C-beta (PLC-beta), also known as NORPA. The molecular and biochemical details of this functional link are unknown. InaD directly binds to NORPA via two terminally positioned PDZ1 and PDZ5 domains. PDZ1 binds to the C-terminus of NORPA, while PDZ5 binds to an internal region overlapping with the G box-homology region (a putative G protein-interacting site). Altered NORPA proteins lacking binding sites display normal basal PLC activity but can no longer associate with InaD in vivo. These truncations cause significant reduction of NORPA protein expression in rhabdomeres and severe defects in phototransduction. Thus, the two terminal PDZ domains of InaD, through intermolecular and/or intramolecular interactions, are brought into proximity in vivo. Such domain organization allows for the multivalent InaD-NORPA interactions, which are essential for G protein-coupled phototransduction (van Huizen, 1998).

Visual transduction in Drosophila is a G protein-coupled phospholipase C-mediated process that leads to depolarization via activation of the transient receptor potential (TRP) calcium channel. Inactivation-no-afterpotential D (InaD) is an adaptor protein containing PDZ domains known to interact with TRP. Immunoprecipitation studies indicate that InaD also binds to eye-specific protein kinase C (INAC) and the phospholipase C, no-receptor-potential A (NORPA). By overlay assay and site-directed mutagenesis the essential elements of the NORPA-InaD association have been defined and three critical residues in the C-terminal tail of NORPA, required for the interaction, have been identified. These residues, Phe-Cys-Ala, constitute a novel binding motif distinct from the sequences recognized by the PDZ domain in InaD. To evaluate the functional significance of the InaD-NORPA association in vivo, transgenic flies were derived expressing a modified NORPA that lacks the InaD interaction: NORPAC1094S. The transgenic animals display a unique electroretinogram phenotype characterized by slow activation and prolonged deactivation. Double mutant analysis suggests a possible inaccessibility of eye-specific protein kinase C to NORPAC1094S, undermining the observed defective deactivation. Similarly, delayed activation may result from NORPAC1094S being unable to localize in close proximity to the TRP channel. It is concluded that InaD acts as a scaffold protein that facilitates NORPA-TRP interactions required for gating of the TRP channel in photoreceptor cells (Shieh, 1997).

Drosophila eye-specific protein kinase C (eye-PKC) is involved in light adaptation and deactivation. eye-PKC, NORPA (phospholipase Cbeta), and transient-receptor-potential (TRP) (calcium channel) are integral components of a signal transduction complex organized by INAD, a protein containing five PDZ domains. There is a direct association between the third PDZ domain of INAD with TRP, and the carboxyl-terminal half of INAD with the last three residues of NORPA. The molecular interaction between eye-PKC and INAD is defined via the yeast two-hybrid and ligand overlay assays. The second PDZ domain of INAD interacts with the last three residues in the carboxyl-terminal tail of eye-PKC, Thr-Ile-Ile. The association between eye-PKC and INAD is disrupted by an amino acid substitution (Ile-700 to Asp) at the final residue of eye-PKC. In flies lacking endogenous eye-PKC (inaCp215), normal visual physiology is restored upon expression of wild-type eye-PKC, whereas the eye-PKCI700D mutant is completely inactive. Flies homozygous for inaCp209 and InaDp215, a mutation that causes a loss of the INAD-TRP association, were generated. These double mutants display a more severe response inactivation than either of the single mutants. Based on these findings, it is concluded that the in vivo activity of eye-PKC depends on its association with INAD and that the sensitivity of photoreceptors is cooperatively regulated by the presence of both eye-PKC and TRP in the signaling complex (Adamski, 1998).

Yeast two-hybrid and ligand overlay results both indicate that the second PDZ domain of INAD associates predominantly with eye-PKC, whereas no interaction was detected with PDZ4. This result is different from a previous report in which interaction of eye-PKC with the fourth PDZ domain of INAD was detected by affinity chromatography (Tsunoda, 1997). The current study tested a total of five constructs that contain the fourth PDZ domain: no indication of eye-PKC/fourth PDZ interaction was found. The constructs tested included a fusion protein that contained exactly the same region as previously tested. One possible explanation for these conflicting results is that the different assay systems are measuring different types of association between eye-PKC and INAD. INAD may bind and cluster eye-PKC to the signaling complex, and it can also act as a substrate for the kinase activity (Huber, 1996a). Amino acid substitutions made in the second PDZ domain of INAD have been shown to disrupt the eye-PKC binding. None of these amino acid changes are near the serine or threonine residues that are putative PKC phosphorylation sites. Furthermore, mutations in the carboxyl-terminal tail of PKC abolish PKC binding to the second PDZ domain. Thus the interaction described for eye-PKC/INAD is a typical carboxyl-terminal tail/PDZ domain association. The basis of the reported interaction with the fourth PDZ domain remains to be determined. Another provocative explanation could be that eye-PKC may bind different PDZ domains of INAD during different physiological conditions. For example, phosphorylation of INAD may change the relative affinity of the interaction in PDZ2 and PDZ4. Clarification of the role of these two eye-PKC/INAD interactions will require analysis of transgenic flies expressing a modified InaD in which these PDZ domain are mutated (Adamski, 1998).

Ceramide kinase regulates phospholipase C and phosphatidylinositol 4, 5, bisphosphate in phototransduction

Phosphoinositide-specific phospholipase C (PLC) is a central effector for many biological responses regulated by G-protein-coupled receptors including Drosophila phototransduction where light sensitive channels are activated downstream of NORPA, a PLCbeta homolog. This study shows that the sphingolipid biosynthetic enzyme, Ceramide kinase, is a novel regulator of PLC signaling and photoreceptor homeostasis. A mutation in Ceramide kinase specifically leads to proteolysis of NORPA, consequent loss of PLC activity, and failure in light signal transduction. The mutant photoreceptors also undergo activity-dependent degeneration. Furthermore, it was showm that a significant increase in ceramide, resulting from lack of ceramide kinase, perturbs the membrane microenvironment of phosphatidylinositol 4, 5, bisphosphate (PIP2), altering its distribution. Fluorescence image correlation spectroscopic studies on model membranes suggest that an increase in ceramide decreases clustering of PIP2 and its partitioning into ordered membrane domains. Thus ceramide kinase-mediated maintenance of ceramide level is important for the local regulation of PIP2 and PLC during phototransduction (Dasgupta, 2009).

This study shows that DCERK regulates the ceramide level to maintain PLC and membrane organization of PIP2 during phosphoinositide-mediated GPCR signaling in Drosophila. These results are summarized in a model depicted in a Model showing ceramide kinase regulates PLC activity, function and the local organization of PIP2 in GPCR signaling. Morphometric analysis of PIP2 clusters suggests that there are still some clusters in dcerk1; thus, the loss of NORPA in dcerk mutant may not be due only to the loss of PIP2 clustering. Although the effect of ceramide on PIP2 is central, increased ceramide could affect other membrane properties that can downregulate NORPA or other proteins. Also, INAD is required for localization of NORPA and TRP is required for localization of INAD. Because TRP protein is affected over time in dcerk1, additional interactions mediated by INAD and TRP could also contribute to NORPA stability. Photoreceptor degeneration seen in cerk mutants is also not simply caused by loss of NORPA protein, as it is more severe and sets in earlier than in norpA null mutants. There could be other effects of ceramide contributing to degeneration (Dasgupta, 2009).

Recent clinical studies have identified mutations in the human ceramide kinase like (CERKL) gene in patients with autosomal recessive retinitis pigmentosa. No CERKL homolog has been identified in the Drosophila genome. Interestingly, DCERK shares 31% identity with human CERKL, and possibly DCERK could perform some CERKL functions also. It would be worthwhile to test whether CERK regulates PLCβ4, the closest homolog of NORPA among mammalian PLCs, thereby participating in the mammalian visual process. Recent analyses of cerk-/- mice revealed that CERK could function in cerebellar Purkinje cells (which are also enriched in PLC?4) and in neutrophil homeostasis. Because the mechanism by which mammalian CERK regulates these processes is not known, it would be interesting to test whether these functions are also mediated through PLC. Although current understanding limits a direct co-relationship between mammalian CERK and PLCs, it is likely that similar ceramide-regulated microenvironments could operate in other phosphoinositide-dependent signaling such as insulin signaling in adipocytes (Dasgupta, 2009).

In summary, these data show that modulation of the ceramide level by CERK regulates PIP2 and PLCβ function in Drosophila. Because PIP2 and PLC are fundamental components of GPCR signaling, uncovering their regulation by ceramide through CERK should lead to a better understanding of lipid regulation in signaling (Dasgupta, 2009).


DEVELOPMENTAL BIOLOGY

Adult

The norpA gene encodes a 7.0-kilobase transcript that can be detected in the head but not in the body of adult flies and a 5.6-kilobase transcript that can be detected throughout development and in both heads and bodies of adults. In situ hybridization of cDNA sequences to tissue sections shows that the gene is expressed in the neuronal cell bodies of the optic lobe, central brain, and thoracic ganglia of adults and the brain of larvae. This tissue distribution of norpA transcripts is identical to the distribution of transcripts from a Drosophila Go alpha-subunit gene (Shortridge, 1991).

Antisera against NorpA recognize an eye-specific protein of 130-kDa relative molecular mass that is present in wild-type head extracts but not in those of strong NorpA mutants. The protein is associated with membranes and can be extracted with high salt. Immunohistochemical analysis at the light and electron microscopic levels indicates that the protein is expressed in all adult photoreceptor cells and specifically localized within the rhabdomeres, preferentially adjacent to, but not within, the rhabdomeric membranes. The results of the present study strongly support the previous suggestion that the norpA gene encodes the major phosphoinositol-specific phospholipase C in the photoreceptors. Moreover, insofar as the rhabdomeres are specialized structures for photoreception and phototransduction, specific localization of the NorpA protein within these structures, in close association with the membranes, is consistent with the proposal that it has an important role in phototransduction (Schneuwly, 1991).

Northern analysis, Western blots, phospholipase C activity assays, and immunohistochemical staining of tissues were all used to examine the tissue-specific expression of the norpA gene. It is expressed in a variety of tissues in addition to the eye. Hybridization of norpA cRNA probe to blots of poly(A+) RNA reveals that the gene encodes at least four transcripts: a 7.5-kilobase (kb) transcript that is expressed in eye and 6.5-, 5.5-, and 5.0-kb transcripts that are expressed in adult body or early stages of development. The 7.5-kb transcript is missing from eyes absent mutants and norpA mutants. Antiserum generated against the major gene product of norpA recognizes a 130-kDa protein that is abundant in eyes but severely reduced or absent in norpA mutants. The NorpA antiserum also recognizes a 130-kDa protein in adult legs, thorax, and male abdomen, but not female abdomen. These localizations are supported by results of phospholipase C activity assays that show that the norpA mutation reduces phospholipase C activity in each of the tissues in which NorpA protein can be detected. Furthermore, immunohistochemical staining of tissue sections with the NorpA antiserum demonstrates that the NorpA protein is abundant in the retina and ocelli and is present to a lesser extent in the brain and thoracic nervous system. Staining in the brain is strongest in the optic lobes and cerebrum. Since some of the above mentioned tissues that express NorpA (such as thorax, legs, and abdomen) have no known photoreceptor tissue, it has been concluded that the norpA gene product is also likely to have a role in signaling pathways other than phototransduction (Zhu, 1993).


EFFECTS OF MUTATION

Eight norpA mutants have been characterized by electroretinogram (ERG), Western, molecular, and in vitro PLC activity analyses. ERG responses of the mutants show allele-dependent reductions in amplitudes and retardation in kinetics. The mutants also exhibit allele-dependent reductions in in vitro PLC activity levels and greatly reduced or undetectable NorpA protein levels. Three carry a missense mutation and five carry a nonsense mutation within the norpA coding sequence. In missense mutants, the amino acid substitution occurs at residues highly conserved among PLCs. These substitutions reduce the levels of both the NorpA protein and the PLC activity, with the reduction in PLC activity being greater than can be accounted for simply by the reduction in protein. The effects of the mutations on the amount and activity of the protein are much greater than their effects on the ERG, suggesting an amplification of the transduction signal at the effector (NorpA) protein level. Transgenic flies were generated by germline transformation of a null norpA mutant using a P-element construct containing the wild-type norpA cDNA driven by the ninaE promoter. Transformed flies show rescue of the electrophysiological phenotype in R1-R6 photoreceptors, but not in R7 or R8. The degeneration phenotype of R1-R6 photoreceptors is also rescued (Pearn, 1996).

Mutations in the norpA gene of Drosophila severely affect the light-evoked photoreceptor potential with strong mutations rendering the fly blind. The norpA gene has been proposed to encode phosphatidylinositol-specific phospholipase C (PLC). A chimeric norpA minigene was constructed by placing the norpA cDNA behind an R1-6 photoreceptor cell-specific rhodopsin promoter. This minigene was transferred into norpAP24 mutants by P-element-mediated germline transformation to determine whether it could rescue the phototransduction defect concomitant with restoring PLC activity. Western blots of head homogenates stained with NorpA antiserum show that NorpA protein is restored in heads of transformed mutants. Moreover, transformants exhibit a large amount of measurable PLC activity in heads, whereas heads of norpAP24 mutants exhibit very little to none. Immunohistochemical staining of tissue sections using NorpA antiserum confirm that expression of NorpA protein in transformants localizes in the retina, more specifically in rhabdomeres of R1-6 photoreceptor cells, but not R7 or R8 photoreceptor cells. Furthermore, electrophysiological analyses reveal that transformants exhibit a restoration of light-evoked photoreceptor responses in R1-6 photoreceptor cells, but not in R7 or R8 photoreceptor cells. This is the strongest evidence thus far supporting the hypothesis that the norpA gene encodes phospholipase C, which is utilized in phototransduction (McKay, 1995).

The norpA (no receptor potential) mutant of Drosophila melanogaster has a visual transduction deficit. This study determines whether lack of function leads to structural repercussions in photoreceptor cells of the compound eye and their synapses. For this purpose, thin sections and freeze fracture replicas of norpA were examined using transmission electron microscopy. Ultrastructurally, retinula cells in the compound eye and all aspects of the first optic neuropil (lamina ganglionaris) are essentially normal in newly emerged flies. However, as expected, intraretinular pigment granules fail to show their light elicited aggregation; further, the P face particle density is somewhat lower than in wild type. There are unusual membrane specializations on the plasmalemma of the retinula cell, dubbed 'zippers'. Zippers appear to increase with age and can cause a distorted geometry of ommatidia. Only a few retinula cells ultimately degenerate in norpA, and the proportion may not differ from that of wild type. Despite the absence of the receptor potential in norpA, many aspects of the turnover of rhabdomeric membrane appear to be as in wild type (Stark, 1989).

The electrophysiological characteristics of norpAH52, a temperature sensitive phototransduction mutant of Drosophila melanogaster, were studied in vivo. Upon raising the environmental temperature to 33-37 degrees C, mutant flies exhibit time-dependent changes in photoresponses. Initial observations indicate losses in responsiveness at low light intensities and prolonged receptor potential waveforms. Subsequently, reductions in response amplitudes at higher light intensities occur, until no responses are obtained. On return to lower temperature the electrophysiological properties recover in reverse order. Based on these observations it is concluded that the primary defect of norpA affects the efficiency of the phototransduction process. Enhanced light exposure can offset the receptor potential changes in norpA. With the temperature sensitive mutant, (1) additional light exposure prolongs the time that responses can be observed at the higher temperature; (2) when 1-s illuminations no longer elicit responses at the higher temperature, 1-min illuminations at the same intensity temporarily restores the ability to obtain 1-s-responses, and (3) light accelerates the restoration of responses on return to lower temperatures. Illumination also has an effect on non-temperature sensitive norpA mutants, enabling the production of small photoresponses in norpAH44, a mutant that normally does not exhibit any responses, and improving the low-light-intensity responses of norpAP16. The current study indicates that the PI cycle, which is inhibited in norpA mutants (Yoshioka, 1985), is an important light-sensitive positive step or effector in the production of receptor potential responses (Wilson, 1987).

The norpAH44 phototransduction mutant of Drosophila, an allele that, on eclosion, does not exhibit a receptor potential was found, at later ages, to undergo light and temperature dependent degeneration of its photoreceptors as well as decreases in rhodopsin concentration. Pseudopupil measurements and light and electron microscopy were used to monitor the structure of the photoreceptors. When norpAH44 flies are maintained exclusively in the dark, no changes in structure or rhodopsin concentration are observed. When maintained on a 12 h light-12 h dark cycle, structural changes are first observed at 6 days of age for flies maintained at 24 degrees C or at 12 days of age for flies maintained at 19 degrees C. When the light-dark cycle is initiated after 10 days in the dark there is a more rapid loss of rhodopsin concentration and pseudopupil. The data suggest that even in the dark, although no obvious changes in structure or rhodopsin concentration are observed, certain processes that support these components have been affected. NorpAP12, an allele that exhibits small receptor potential amplitudes, also displays age- and light-dependent photoreceptor degeneration and decreases in rhodopsin concentration, whereas no degeneration or decreases in rhodopsin are observed in norpAP16, an allele that exhibits receptor potential amplitudes similar to those of wild-type. The data suggest that the processes that affect phototransduction, such as the phosphatidylinositol cycle, have a long-term role in the maintenance of rhodopsin concentration and photoreceptor integrity (Meyertholen, 1987).

The formation of stable rhodopsin-arrestin complexes induces apoptosis and photoreceptor cell degeneration

Although many different mutations in humans and Drosophila cause retinal degeneration, in most cases, a molecular mechanism for the degeneration has not been found. This study demonstrates the existence of stable, persistent complexes between rhodopsin and its regulatory protein arrestin in several different retinal degeneration mutants. Elimination of these rhodopsin-arrestin complexes by removing either rhodopsin or arrestin rescues the degeneration phenotype. Furthermore, it is shown that the accumulation of these complexes triggers apoptotic cell death and that the observed retinal degeneration requires the endocytic machinery. This suggests that the endocytosis of rhodopsin-arrestin complexes is a molecular mechanism for the initiation of retinal degeneration. It is proposed that an identical mechanism may be responsible for the pathology found in a subset of human retinal degenerative disorders (Alloway, 2000).

This paper demonstrates the existence of a novel mechanism to explain the light-dependent retinal degeneration that is observed in a subset of Drosophila visual system mutants. Mutations in three distinct genetic loci, norpA, arr2, and rdgB, result in the light-dependent formation of stable rhodopsin-arrestin complexes. Elimination of either member of this complex rescues the retinal degeneration in each of the three genetic backgrounds. In addition, it is shown that the formation of these stable rhodopsin-arrestin complexes triggers apoptotic cell death. Furthermore, endocytosis is essential for inducing cell death in norpA mutants, suggesting that the internalization of the rhodopsin-arrestin complexes is an early step in the initiation of apoptosis of retinal photoreceptors. It is possible that the excessive endocytosis saturates a downstream cellular function (for example, saturation of the early endosome or depletion of an endocytic protein), which signals the cell to undergo programmed cell death. Alternatively, the endocytosis may block a signal that protects the cell from apoptosis (Alloway, 2000)

The inactivation of the Drosophila phototransduction cascade is an extremely rapid event. Drosophila photoreceptors can shut off the light-activated currents in less than a 100 ms following termination of the light stimulus. One way in which photoreceptors have evolved to do this is at the level of the G protein-coupled receptor rhodopsin. Immediately upon activation, rhodopsin is multiply phosphorylated on its C terminus, and this phosphorylation greatly increases its affinity for the abundant soluble protein arrestin. Invertebrate Arr2 is a very basic molecule with a pKa of ~8.7 and, therefore, has a high affinity for phosphorylated rhodopsin. Thus, this interaction of activated rhodopsin and arrestin occurs very rapidly, and the receptor is quickly inactivated. It is tempting to speculate that the posttranslational modifications of arrestin and rhodopsin are essential to eliminate these complexes. In such a model, it is necessary to phosphorylate Arr2, thereby making it less basic, as well as to dephosphorylate rhodopsin, thereby making it less acidic. Thus, the system is designed such that the influx of calcium activates CamKII, the kinase that phosphorylates arrestin, and rdgC, the phosphatase that dephosphorylates rhodopsin. Both of these steps are crucial, as evidenced by the fact that rdgC mutants and arr2(S366A) mutants both undergo rapid light-dependent retinal degeneration. Evidence suggests that, in the absence of these posttranslational modifications, stable rhodopsin-arrestin complexes persist in the cell and are instrumental in the pathology of retinal degeneration (Alloway, 2000)

The retinal degeneration induced by rhodopsin-arrestin complexes can be partially rescued by a temperature-sensitive allele of dynamin. This observation suggests that the rhodopsin-arrestin complexes are being removed from the photoreceptor rhabdomere by the endocytic machinery. A similar receptor internalization pathway occurs for the vertebrate β-adrenergic receptor. β-arrestin is involved in the inactivation and internalization of the β-adrenergic receptor. A small domain near the carboxyl terminus of β-arrestin directly interacts with clathrin and targets the β-adrenergic receptor-β-arrestin complex for internalization. This clathrin binding site is curiously missing in the visual arrestins. However, in spite of the absence of the clathrin-interacting motif, these complexes seem to have the ability to interact with the endocytic machinery. One attractive model is that visual arrestin serves as an AP2-like adaptor, just like β-arrestin, but recruits clathrin by a different mechanism. The question of whether the endocytic proteins are recognizing motifs in rhodopsin or arrestin awaits further studies. Many models have been proposed to explain retinal degeneration in humans, including constitutive activity of the phototransduction cascade, improper trafficking of photoreceptor cell components, and defects in the recycling of rhodopsin. The results described in this study implicate the endocytic pathway in retinal degeneration and suggest that excessive endocytosis can be a trigger for apoptotic cell death (Alloway, 2000)

The internalization of rhodopsin-arrestin complexes via receptor-mediated endocytosis could partly explain the membrane association of arrestin in certain mutant backgrounds. The enhanced membrane affinity of arrestin could in part be due to the rhodopsin-arrestin complexes rapidly interacting with the endocytic machinery. It is possible that, once the complex is associated with clathrin cages, the arrestin would be locked in the membrane-associated state. In support of this model, it has recently been demonstrated that the unphosphorylated form of arrestin directly interacts with clathrin in vitro. Therefore, it is possible that the role of arrestin phosphorylation is to block interactions with clathrin, and any mutant background that fails to phosphorylate arrestin yields complexes due to clathrin interactions. However, it is still essential that a stable rhodopsin-arrestin complex be formed initially to allow for the assembly of the endocytic proteins (Alloway, 2000)

A large number of mutations in the human rhodopsin gene have been isolated that are responsible for retinal disease. Interestingly, there are several mutations in human rhodopsin that form stable rhodopsin-arrestin complexes. These include a mutation in a highly conserved lysine in the seventh transmembrane domain that has been shown to cause autosomal-dominant retinitis pigmentosa. This mutant form of rhodopsin is found both in vivo and in vitro to be constitutively phosphorylated and tightly bound to arrestin. It had been hypothesized that the complexes between rhodopsin and arrestin may be instrumental in the retinal degeneration process. Possibly, as in Drosophila, these stable human rhodopsin-arrestin complexes are removed from the rod outer segments by the endocytic machinery, and this excessive endocytosis is the direct cause of apoptotic retinal degeneration (Alloway, 2000)

One question yet to be addressed is why photoreceptor cells have a mechanism for eliminating rhodopsin-arrestin complexes if, under nonpathological conditions, these complexes do not persist in the cell. One possible explanation is that arrestin has a secondary function to eliminate defective rhodopsin molecules from the photoreceptor cell. A rhodopsin molecule that becomes photochemically damaged may render the receptor nonfunctional or constitutively active. The presence of a constitutively active rhodopsin molecule could potentially be very detrimental and, therefore, necessitates its removal from the photoreceptor cell. Presumably, any rhodopsin molecule that becomes constitutively active will bind arrestin and generate a stable rhodopsin-arrestin complex. The stabily bound arrestin would target the dysfunctional rhodopsin molecule for endocytosis and degradation. In this manner, arrestin could function as a surveillance protein, eliminating defective rhodopsin molecules from the photoreceptor cell. However, in certain mutant backgrounds, the regulation of rhodopsin-arrestin complex formation is defective, and a large number of complexes are formed. The increased endocytosis of these complexes initiates apoptosis and retinal degeneration (Alloway, 2000).

Photoreceptor cells adapt to bright or continuous light, although the molecular mechanisms underlying this phenomenon are incompletely understood. This paper reports a mechanism of light adaptation in Drosophila, which is regulated by phosphoinositides (PIs). Light-dependent translocation of arrestin is defective in mutants that disrupt PI metabolism or trafficking. Arrestin binds to PIP(3) in vitro, and mutation of this site delays arrestin shuttling and results in defects in the termination of the light response, which is normally accelerated by prior exposure to light. Disruption of the arrestin/PI interaction also suppresses retinal degeneration caused by excessive endocytosis of rhodopsin/arrestin complexes. These findings indicate that light-dependent trafficking of arrestin is regulated by direct interaction with PIs and is required for light adaptation. Since phospholipase C activity is required for activation of Drosophila phototransduction, these data point to a dual role of PIs in phototransduction (Lee, 2003).

The demonstration that translocation of Arr2 is regulated by PIs addresses a lingering question concerning potential roles of PIs in photoreceptor cells. The Drosophila visual transduction cascade is among the most intensively studied GPCR cascades. During the last 30 years, many proteins and mutations have been identified that perturb PI signaling; however, the targets and mechanisms directly regulated by PIs have not been previously described (Lee, 2003).

The regulation of Arr2 shuttling by PIs occurs on the order of a few to many minutes. This is in contrast to the millisecond time scale, which operates in the activation of phototransduction. Although the specific activation mechanism involved in Drosophila phototransduction remains elusive, it is established that it depends on a PLCβ (NORPA). Thus, PLC-mediated hydrolysis of PIP2 leads to rapid activation of the light-sensitive channels through the millisecond generation of PIP2 metabolites or reduction in PIP2 levels. Since adaptation occurs over a much slower timescale, regulation of this latter phenomenon exclusively by direct effects of second messengers on protein activities might be too rapid. Rather, regulation of adaptation by the translocation of signaling proteins provides a mechanism whereby changes in second messengers, such as PIP3, result in delayed effects on the magnitude and the kinetics of signaling. Therefore, PIs appear to have the capacity to serve a dual role in activation and adaptation by modulating the activities and localization of signaling proteins (Lee, 2003).

Previous reports have shown that stable Arr2/rhodopsin complex formation leads to retinal degeneration in norpA or rdgC flies. Removal of the arr2 gene in a norpA or rdgC background partially suppresses the photoreceptor cell death. This partial suppression could be due to elimination of Arr2/rhodopsin complexes, reduction in endocytosis of rhodopsin, or disruption of some other Arr2 function. In this work, Arr2/rhodopsin binding and PI-regulated trafficking of Arr2 were uncoupled by expressing Arr23K/Q, which is defective in movement but not rhodopsin binding. Since the retinal degeneration in norpA is largely rescued in arr23K/Q flies, these results suggest that apoptosis in norpA results from endocytosis of Arr2/rhodopsin complexes rather than a defect in Arr2/rhodopsin binding. This conclusion is further supported by the finding that there was even greater suppression of the norpA degeneration in an arr23K/Q than in an arr25 null background (Lee, 2003).

Molecular basis of amplification in Drosophila phototransduction: Roles for G Protein, Phospholipase C, and Diacylglycerol kinase

In Drosophila photoreceptors, the amplification responsible for generating quantum bumps in response to photoisomerization of single rhodopsin molecules has been thought to be mediated downstream of phospholipase C (PLC), since bump amplitudes were reportedly unaffected in mutants with greatly reduced levels of either G protein or PLC. It is found that quantum bumps in such mutants are reduced ~3- to 5-fold but are restored to near wild-type values by mutations in the rdgA gene encoding diacylglycerol kinase (DGK) and also by depleting intracellular ATP. The results demonstrate that amplification requires activation of multiple G protein and PLC molecules; they identify DGK as a key enzyme regulating amplification, and implicate diacylglycerol as a messenger of excitation in Drosophila phototransduction (Hardie, 2002).

Many photoreceptors generate discrete responses to effective absorptions of single photons, known as quantum bumps. In Drosophila, these represent simultaneous activation of about 15 light-sensitive channels generating an inward current of ~10 pA. The response is remarkable for its speed, with latencies as short as 20 ms and bump halfwidths of ~20 ms. These kinetics are about 100 times faster than in toad rods recorded at similar temperatures, about 10 times faster than mammalian rods recorded at 37°C, and in general, fly photoreceptors are considered to have the fastest known G protein-coupled signaling cascades. The events leading to quantum bump generation in Drosophila have been inferred from a variety of physiological, biochemical, and genetic evidence. Photoisomerized rhodopsin activates a heterotrimeric G protein (Gq class) releasing the alpha subunit, which in turn activates phospholipase C (PLCß4 isoform) encoded by the norpA gene. By a still unknown mechanism, activation of PLC leads to the opening of at least two classes of Ca2+ permeable channels, TRP and TRPL. These are the prototypical members of the TRP ion channel superfamily responsible for a wide variety of Ca2+ influx pathways throughout the body. Recent evidence suggests that the Drosophila channels, as well as some vertebrate TRP homologs, may be activated by lipid second messengers rather than by InsP3. Candidates include diacylglycerol (DAG), polyunsaturated fatty acids (PUFAs), which are DAG metabolites, or a reduction in phosphatidyl inositol 4,5 bisphosphate (PIP2). Following activation of the first channel(s), Ca2+ influx mediates rapid positive and negative feedback, which is required for both amplification and rapid termination of the quantum bump. Most, if not all, elements of the phototransduction cascade are located in the ~30,000 tightly packed microvilli, each only 60 nm in diameter and 1–2 µm long, which together form the light-guiding rhabdomere. Quantitative Western analysis suggests that there are about 25 TRP channels per microvillus, which corresponds closely to the number of channels activated during the quantum bump. It is therefore plausible that quantum bump generation is restricted to a single microvillus, representing activation of all or most of the available channels (Hardie, 2002).

In contrast to the situation in vertebrate rods, recent evidence has led to the proposal that all amplification in this system is mediated downstream of PLC. The main evidence for this view is that quantum bump amplitude is reported to be unaffected in hypomorphic mutants of G protein (Gaq) and PLC (norpA) where protein levels are reduced to levels (<1%) such that there may often be no more than a single G protein or PLC molecule in each microvillus. This led to the conclusion that levels of G protein do not actively contribute to the gain of the single photon response and that the G protein must act as a 'molecular switch,' triggering bump generation (Hardie, 2002).

In the present study, this view has been questioned because of the observation of spontaneous events in the dark in WT flies. Although the data suggested they were due to spontaneous activation of G proteins, they are much smaller than quantum bumps, seemingly inconsistent with single G proteins triggering full-sized bumps. Quantum bumps were therefore systematically reinvestigated in both Gaq and norpA hypomorphs; contrary to previous reports, bump amplitudes were much reduced, suggesting that there is substantial amplification upstream of PLC. The discrepancy with earlier studies is resolved by showing that bump amplitude in both Gaq and norpA mutants could be increased to near WT levels by omitting ATP from the whole-cell recording pipette. Finally, DAG kinase has been identified as the critical ATP-dependent factor, strongly supporting the proposal that DAG (or its downstream metabolites) is the excitatory messenger responsible for channel activation (Hardie, 2002).

The current view that amplification in the Drosophila phototransduction cascade is mediated downstream of PLC is based largely on reports that bump amplitude and timecourse are unaffected in mutants of G protein or PLC. However, after testing an extensive range of mutants of both G protein and PLC, it was found that in all cases quantum bump amplitude was greatly reduced. Although these results seemed to directly contradict earlier studies, it was found that when ATP was omitted from the electrode, bump amplitude approached WT values. This almost certainly accounts for the apparently conflicting results (Hardie, 2002).

Cook (2000) analyzed bump in detail only from norpAC1094S flies, which this study has found to have among the largest bumps of the norpA alleles tested (~3 pA with occasional bumps as large as 10 pA). Since Cook (2000) excluded events less than 3 pA in amplitude from their analysis, their results are not necessarily in conflict with the results of this study: small bumps are indeed found, e.g., with norpAP57 under similar recording conditions. Most significantly, the effect of removing ATP could be closely mimicked by mutations in the rdgA gene encoding DGK. These results indicate that amplification in Drosophila is critically dependent on activation of multiple G protein and PLC molecules and identify DGK as a key enzyme regulating bump amplitude and inactivation (Hardie, 2002).

It is now concluded that amplification in Drosophila phototransduction is critically dependent upon activation of multiple G proteins and PLC molecules. Assuming linear summation, the difference in bump current integral between WT and the most severe Gq and norpA hypomorphs suggests that at least five PLCs need be activated in order to generate a typical WT bump. Since quantum bumps in Drosophila correspond to the simultaneous opening of only about 15 channels at the peak of the bump, amplification at the level of the G protein may in fact represent the major component of amplification in Drosophila. Interestingly, a similar number of G proteins (about eight) are believed to be activated in Limulus ventral photoreceptors, although amplification downstream of PLC dominates in these cells -- probably by very distinct mechanisms (Hardie, 2002).

Significantly, lowering ATP did not further increase bump amplitude in WT photoreceptors, suggesting that the bump-generating machinery is saturated in dark-adapted photoreceptors. This can be understood if quantum bumps represent activation of all available channels within the microvillus. The suggestion that the unit of signaling underlying the quantum bump is the microvillus is also consistent with the finding that the number of channels activated during the quantum bump corresponds closely to the number predicted per microvillus from quantitative Western analysis (Hardie, 2002).

Is DAG the excitatory messenger? The essential role of PLC in Drosophila phototransduction is well established, but the downstream mechanisms responsible for gating the light-sensitive channels remain controversial. Accumulating evidence, including the lack of phenotype in mutants of the only InsP3 receptor gene known in Drosophila, suggests that InsP3 may not be involved in excitation. Additional consequences of PLC activation include generation of DAG and a reduction in PIP2, both of which are also currently under discussion as excitatory messengers for some vertebrate TRP homologs. Both TRP and TRPL channels can be activated by polyunsaturated fatty acids (PUFAs), which might be released from DAG by a DAG lipase. It has been found that heterologously expressed TRPL channels can also be activated by DAG, raising the possibility that DAG may be the endogenous transmitter, with PUFAs mimicking their action. However, at least some of the actions of DAG and PUFAs may be indirect via activation of endogenous PLC; activity of TRPL channels in patches is suppressed by application of PIP2, suggesting PIP2 depletion as a potential contributory factor to channel gating (Hardie, 2002).

The analysis of the DGK mutant rdgA in this study provides strong independent evidence for an excitatory role for DAG. TRP and TRPL channels in rdgA mutants are constitutively active and degeneration is largely prevented in rdgA;trp double mutants. The response to light is also rescued in rdgA;trp, revealing a deactivation defect, suggesting a role for DGK in response termination, at least with respect to TRPL channels. These results would be consistent with a role for DAG in excitation; however, DGK is also the first enzyme in the PIP2 recycling pathway, so that PIP2 levels may also be affected in the rdgA mutant. Furthermore, the remaining TRPL channels were still constitutively active in the rdgA;trp double mutant, and light responses could only be compared to controls in pupae during a very narrow developmental time window (Hardie, 2002).

In the present study, rdgA double mutants were generated with both Galphaq1and norpA, allowing analysis in adult flies with intact TRP and TRPL channel function. Strikingly, bump amplitudes in both norpA and Galphaq1 are restored to WT levels by rdgA mutations, also showing defects in inactivation. In addition, quantum efficiency (Q.E. -- the percentage of absorbed photons eliciting a bump) is enhanced, resulting in some cases in massive (~100-fold) overall increases in sensitivity. Since the evidence indicates that these rdgA phenotypes are not due to reduced PIP2 levels, this is interpreted as compelling evidence for the role of DAG as messenger of excitation. DAG levels are dynamically determined by the balance between PLC activity (generating DAG from PIP2) and DGK activity (converting DAG to PA). It seems that when only one PLC molecule is activated, DAG is metabolized too quickly for threshold levels to be reached, except perhaps in the immediate vicinity of the activated PLC. However, if DGK is inactivated by the rdgA mutation or by depleting ATP, then DAG can reach threshold more readily and also diffuse to activate more distant channels so that quantum efficiency and quantum bump amplitudes approach WT values. (Note that the reduction in Q.E. in Gaq1 has been attributed to most activated rhodopsins being inactivated before they have a chance to encounter a rare G protein; the results of this study suggest that a major factor in the reduction of Q.E. is that, despite activating a PLC, most single activated G proteins result in insufficient DAG generation to overcome bump threshold). Despite these arguments, a contributory role of PIP2 to channel regulation cannot be excluded. For example, it is conceivable that channels are bound to PIP2 in the closed state, that channel activation involves exchange of PIP2 for DAG, and that channel closure following excitation may involve rebinding of PIP2 (Hardie, 2002).

Multiple, sequential G protein activation is well established as a mechanism of amplification in vertebrate phototransduction. Although it has been concluded that multiple G protein activation is also required for amplification in Drosophila, the molecular strategies remain qualitatively and quantitatively distinct. In rods, each activated G protein rapidly encounters a PDE, which immediately begins to hydrolyze cGMP. The cGMP concentration is sensed continuously by the light-sensitive channels, which progressively close as upward of 100 G protein and PDE molecules are recruited by random diffusional encounters with rhodopsin. This gives rise to quantum bumps with very short latencies, but which rise gradually over a time course of ~1 s in toad or ~100 ms in mammalian rods. In Drosophila and other microvillar photoreceptors, there is a finite and variable latency (~20–100 ms in Drosophila) followed by an abrupt (~10 ms) rising phase, indicative of a threshold and positive feedback—features not found in vertebrate photoreceptors. At rest in the dark, the channels are closed, and the latency presumably represents the time taken for diffusional encounters of, perhaps, five to ten G proteins with rhodopsin and PLC and then for sufficient second messenger (DAG or its PUFA metabolites) to accumulate to activate the first channel. Because of the restricted volume of the microvillus, Ca2+ influx via the first channel raises Ca2+ rapidly throughout the microvillus. If other channels in the microvillus are already exposed to subthreshold concentrations of DAG generated by other PLC molecules, it is proposed that the raised Ca2+ sensitizes these channels (e.g., by increasing the affinity of the channel for DAG/PUFA), resulting in an explosive positive feedback which activates all or most of the channels in the microvillus over a time course of ~10 ms. Ca2+, which reaches concentrations of at least 200 µM, then mediates negative feedback terminating the bump. Finally, there is believed to be a refractory period lasting ~100 ms, while the Ca2+ is cleared by diffusion and/or Na+/Ca2+ exchange and necessary biochemical steps of inactivation (e.g., Rh-arrestin binding, GTPase activity, clearance of DAG, resynthesis of PIP2) run their course (Hardie, 2002).

In summary, the results indicate that amplification in Drosophila phototransduction is critically dependent upon activation of multiple G proteins and PLC molecules, identify DGK as a key enzyme regulating amplification, and strongly support the identification of DAG as messenger of excitation in Drosophila phototransduction. PLC has long been recognized as the effector enzyme in invertebrate phototransduction, playing an analogous role to PDE in vertebrate rods (although PLC generates the active transmitter, while PDE degrades it). The results now suggest that DGK is the key enzyme controlling the supply of second messenger in Drosophila and thus plays an analogous role to guanylate cyclase. Ca2+-dependent regulation of guanylate cyclase is a key mechanism of light adaptation and response termination in vertebrate rods. It will be interesting to see whether similar regulation of DGK is involved in regulating sensitivity and kinetics during light adaptation in Drosophila (Hardie, 2002).

Seasonal behavior in Drosophila melanogaster requires the photoreceptors, the circadian clock, and phospholipase C

Drosophila locomotor activity responds to different seasonal conditions by thermosensitive regulation of splicing of a 3' intron in the period mRNA transcript. The control of locomotor patterns by this mechanism is primarily light-dependent at low temperatures. At warmer temperatures, when it is vitally important for the fly to avoid midday desiccation, more stringent regulation of splicing is observed, requiring the light input received through the visual system during the day and the circadian clock at night. During the course of this study, it was observed that a mutation in the no-receptor-potential-A(P41) [norpA(P41)] gene, which encodes phospholipase-C, generates an extremely high level of 3' splicing. This cannot be explained simply by the mutation's effect on the visual pathway and suggests that norpA(P41) is directly involved in thermosensitivity (Collins, 2004).

The proportion of per transcripts that were spliced at 18°C and 29°C, averaged over several LD 12:12 cycles was examined in Canton-S WT and per01, tim01, cryb, and per01; cryb mutant backgrounds. In all backgrounds splicing levels fall as the temperature rises, with 40%-60% of transcripts spliced at 18°C and 20%-45% at 29°C. However, not all genotypes react in the same way to temperature changes (Collins, 2004).

The smallest but nevertheless significant effect of temperature on splicing levels is observed in per01; cryb, suggesting that the temperature-sensing system for splicing may be compromised in the double mutant. A significant temperature x time effect reveals that the temporal patterns of cycling differ among temperatures, and the absence of any other significant interactions suggests that all genotypes respond similarly. There is very little evidence for a significant day/night cycle in the proportion of per transcripts that are spliced at 18°C, but at 29°C, all genotypes reveal a higher level of splicing post lights off (ZT12) compared to the trough at ZT8. At 18°C, the per01 and tim01 mutations have no significant effect on the level of splicing of per mRNA compared to WT. However in cryb flies, splicing levels are significantly elevated, particularly after lights off. This is also the case when per01; cryb is compared to WT. At 29°C, splicing levels are generally 5%-10% higher in per01, tim01, and cryb mutants compared to WT in the light, but 15%-20% higher after lights off at ZT12. This suggests that in the presence of light, splicing levels are reduced due largely to a clock-independent mechanism. In darkness, the clock and Cry become critical for maintaining this low splicing level at high temperatures (Collins, 2004).

The double mutant per01; cryb shows a highly significant increase in splicing of ~20% throughout the day/night cycle compared to WT. Thus, at high temperature, either the presence of the circadian photoreceptor Cry or a functional circadian clock is sufficient to largely repress daytime splicing. With both eliminated, daytime splicing levels are elevated. In contrast, repression of splicing in the absence of light requires the circadian clock plus Cry. It seems somewhat counterintuitive that Cry, which is activated by light, plays a more prominent role in repressing splicing at night than it does during the day (Collins, 2004).

Cry is likely to be a dedicated circadian photoreceptor yet at 29°C, splicing is repressed during the light phase even in cryb. This suggests that the light input to the splicing machinery cannot be primarily mediated by Cry. To confirm that light represses splicing, the effects that short photoperiods and constant darkness (DD) have on splicing levels in WT was investigated. There is a significant effect of reducing photoperiod on the splicing level with an elevated level of splicing in DD compared to LD 12:12, and similarly in LD 6:18, splicing levels are enhanced. Because the repression of splicing by light in LD 12:12 at 29°C does not require the presence of Cry, whether the visual system plays a role in setting the splicing level was investigated by examining the splicing of per transcripts in the mutants gl60j and norpAP41 (Collins, 2004).

The proportion of per mRNA transcripts that are spliced at both temperatures is increased in both the norpAP41 and gl60j backgrounds compared to WT. At 18°C, ~65% of per transcripts are spliced in norpAP41 and ~60% in gl60j, whereas at 29°C, these levels fall to ~55% and ~40%, respectively. Apart from a marginal difference between norpAP41; cryb, and norpAP41 at 18°C, there are no significant effects for either norpAP41 or gl60j when combined with cryb. These results indicate that the visual system rather than Cry is primarily responsible for the light-dependent repression of splicing. Unlike WT, per splicing levels do not rise after lights off at 29°C in either norpAP41 or gl60j (Collins, 2004).

Interestingly, in gl60j, there is a 20% difference between the splicing levels at different temperatures (60%-40%), whereas in norpAP41, this difference is reduced to 10% (65%-55%). The difference in gl60j is similar to that seen in WT (45%-25%). Thus per splicing in norpAP41 is relatively insensitive to temperature changes. It is also clear that the level of splicing in norpAP41 is significantly higher at all times and temperatures than gl60j. Therefore, the effect of norpAP41 on splicing is greater than that of gl60j, despite gl60j being the more severe visual mutant (Collins, 2004).

Locomotor activity profiles of all genotypes were also monitored at 18°C and 29°C. Because each genotype shows a higher level of splicing at 18°C than at 29°C, it would be predicted that this would generate an earlier evening activity peak at 18°C. This is the case for WT, cryb and norpAP41, but not for norpAP41; cryb or gl60j, where despite elevated splicing levels at higher temperatures, there is no difference in the phase of activity. gl60j cryb does not entrain to LD cycles at 25°C, so was not included in this analysis (Collins, 2004).

The average proportion of per transcripts that are spliced at 18°C rises from WT (45%) to cryb (50%) to gl60j (60%) to norpAP41 (65%), and at 29°C from WT (25%) to gl60j and cryb (~35%) to norpAP41 (55%). If the per splicing level is the only determinant of evening locomotor peak position, then a similar progression in the timing of this peak would be expected. The evening activity peaks of these different genotypes at 18°C and 29°C were compared. For norpAP41, cryb, and WT, there is an inverse relationship between average splicing levels and the position of the activity peak at 18°C, with norpAP41 and cryb having similarly advanced activity peaks compared to WT. At 29°C, the same inverse relationship holds, with norpAP41 advanced compared to cryb, which is in turn earlier than WT. Thus, those genotypes that show temperature-dependent changes in their evening activity generally display a correlation between average per splicing levels and the timing of the evening activity peak of the following day. Conversely, norpAP41; cryb and gl60j,, which show no significant differences in the phase of evening activity at different temperatures, have high splicing levels but relatively delayed evening activity peaks (Collins, 2004).

These observations raise the question of why the splicing level does not always relate to the timing of the evening locomotor activity peak, as in gl60j and norpAP41; cryb. Thus the per RNA profiles of gl60j and norpAP41 were compared to WT. Because per does not cycle in cryb whole head homogenates, the underlying cycle in this background was not examined. WT and norpAP41 show similar profiles, with an earlier per mRNA peak and higher overall level of per at the lower temperature. In contrast, there is no cycle in gl60j at either temperature, and levels of per are significantly different from WT and norpAP41 (Collins, 2004).

Therefore, to entrain locomotor behavior to different seasons, the fly's clock must respond to changes in both light and temperature. This is mediated through a molecular switch, whereby increases in temperature repress the splicing of an intron within the 3' UTR of per, delaying the onset of evening locomotor activity. Light also represses splicing, with higher splicing levels seen in shorter photoperiods, allowing locomotor activity to be fine-tuned to any given set of photoperiodic and temperature conditions. During the first day of DD, the level of splicing rises continuously. This is presumably because at the beginning of DD, the level of splicing is set low from the previous day's light input. Normally the light from the next day maintains this repressed level of splicing, but because this light input is absent, the repression of splicing is lifted, leading to a gradual rise in splicing levels (Collins, 2004).

The most obvious source for light input into the splicing machinery is the circadian photoreceptor Cry. However, analysis of the splicing levels in cryb shows that, although this mutation has an effect on splicing levels at 18°C, this effect is marginal and is seen only after lights off. This implies (1) that any function of Cry in the repression of splicing is not via the activation of this molecule by light; (2) because Cry is relatively dispensable for circadian locomotor rhythmicity per se, it also suggests that any minor role in splicing at low temperature is unrelated to the functioning of the clock. As the temperature rises, Per, Tim, and Cry all become involved in the regulation of per mRNA splicing. At 29°C, all three mutants show the same splicing phenotype, with ~30% of transcripts spliced during the day, but at night splicing is enhanced to ~45%. Although Per, Tim, and Cry are known to associate in light conditions, Cry and Tim can also associate in darkness, so it is not unexpected that the elimination of any one of the three proteins has a similar effect. Night time is also when the levels of these proteins are at their highest, and therefore any effects would be maximal (Collins, 2004).

At 29°C and in the presence of light, the levels of splicing in per01; cryb are elevated above those of either single mutant, which are themselves similar to WT. This suggests that the presence of either Per or Cry is required for light to repress splicing at 29°C. After lights off, the elevated levels of splicing of per are very similar in per01, tim01, cryb, and per01; cryb. Therefore Per, Tim, and Cry probably work together to repress splicing in the dark at 29°C. An alternative view for the virtually identical per01, tim01, and cryb splicing levels at 29°C is that this reflects a masking effect of light, so that exogenous LD cycles have a greater effect on splicing at night compared to WT, which shows a modest but significant day-night rhythm. Such stronger masking effects on locomotor behavior have also been observed in cryb mutants, but any mechanism that might relate or explain these observations remains obscure (Collins, 2004).

The examination of whole head homogenates means that the majority of biological material is derived from the eyes so may not represent exactly what occurs in the pacemaker neurons. The eyes are peripheral clocks, and the cryb mutation stops the cycling of the clock in whole head homogenates, although cycling continues in the pacemaker cells. One possibility is that the splicing observed in cryb does not truly reflect the role of Cry in setting splicing levels but is instead a consequence of the clock having stopped in the eyes, thus explaining why per01, tim01, and cryb all show the same splicing phenotype. However, if this splicing phenotype is simply what happens when the clock stops, then per01; cryb should show the same splicing phenotype as either single mutant. This is not the case, because the daytime splicing in per01; cryb at 29°C is dramatically elevated compared to either single mutant. Thus the splicing phenotypes of per01, tim01, and cryb cannot simply be a result of the clock having stopped. This means that it is the presence of these proteins, rather than their clock-dependent cycling, that is important to the regulation of per splicing levels (Collins, 2004).

In gl60j, there is no per mRNA cycle in whole head homogenates. This means that in the majority of cells in the gl60j head, the clock has either stopped or cells have become desynchronized. If the former is true, then splicing levels of gl60j should resemble those of per01 or tim01, and this is clearly not the case. If the latter is true, this could prevent the observation of any splicing rhythm, but the level of splicing observed should still represent the average level of splicing in this mutant background, which is clearly significantly different from WT. In any case, splicing levels observed in all visual mutants are likely to represent the effect of removing visual photoreception, because these elevated levels are similar to those observed in WT in DD (Collins, 2004).

norpAP41 and gl60j have considerably higher splicing levels than WT and cryb mutants at both temperatures, indicating that information received via the visual system rather than Cry drives this repression of splicing, which is borne out by analysis of gl60j cryb and norpAP41; cryb double mutants. The splicing levels of gl60j and gl60j cryb are similar at both temperatures, which is also true of norpA and norpAP41; cryb at 29°C. At 18°C, there is slightly more spliced per RNA in norpAP41; cryb than in the norpAP41 single mutant, reflecting the earlier result where cryb showed a marginal enhancement of splicing at cooler temperatures. These results also demonstrate that unspecific genetic background effects are not responsible for this marginal effect of cryb, because the double mutant background should make any interacting loci heterozygous. This lack of significant background effects in determining overall splicing levels has been confirmed by examining several natural European D. melanogaster lines. All mutants studied here show the same significantly enhanced splicing patterns when compared to any of the wild-caught isolates (Collins, 2004).

Unlike the clock and cryb mutants, there is no day-night difference in splicing levels at 29°C in either gl60j or norpAP41. One possibility is that visual system structures are required for the repression of splicing even in the dark, hence the overall elevated splicing levels in norpAP41 and gl60j at all times. This would be surprising, because such a role would obviously have to be light independent. More likely, the light input received through the eyes sets the splicing level during the day, and the clock maintains this repression at night. Thus, if the visual input is removed or reduced, as in DD, gl60j, or norpAP41 mutants, or in shorter photoperiods, then the subsequent splicing level is set higher. The difference in roles between cry and the visual system on per splicing levels may also partly explain recent observations that cryb mutants are able to adapt the timing of locomotor activity to long and short photoperiods, whereas flies with defective visual photoreception, including gl60j, are not (Collins, 2004).

Interestingly, although gl60j is the more severe visual mutant, norpAP41 has significantly higher per splicing levels than gl60j at both 18°C and 29°C. Additionally, whereas the difference between splicing levels at 18°C and 29°C is maintained in gl mutants (~65% and ~45% of transcripts spliced vs. ~45% and 25% in WT at 18°C and 29°C, respectively), this is greatly reduced in norpAP41 (65% and 55%). One possible explanation for this is that norpA may be a signaling molecule in the temperature-sensing pathway for the clock. The patterns of locomotor activity support a role for norpA in temperature sensing, with the norpAP41 fly's locomotor patterns seemingly more sensitive to high temperatures than WT. Additionally, norpAP41 evening locomotor activity peaks early at both 18°C and 29°C, and per mRNA splicing shows a corresponding elevation compared to WT. These are responses associated with low temperatures in WT D. melanogaster, and therefore norpAP41 mutants behave as if they have an impaired ability to detect high temperatures. norpAP41 flies still detect temperature changes (witness the altered evening peaks and splicing levels); they just react as if the temperature is colder than it actually is (Collins, 2004).

Thus, the enhanced per splicing seen in norpAP41 may reflect a direct link between norpA-encoded PLC signaling and the temperature sensitivity of the splicing mechanism, independent of norpA visual function. In the phototransduction cascade, rhodopsin activates a G-protein isoform that in turn activates the PLC encoded by norpA. As a result of this activation, Ca2+ permeable light-sensitive channels are opened, including members of the transient receptor potential (TRP) class. Recently it has been demonstrated that dANKTM1, a D. melanogaster TRP channel, is activated by temperatures from 24°C to 29°C. In addition, D. melanogaster painless mutant larvae have a disrupted TRP channel and display defective responses to thermal stimuli. Because several TRP family members act as thermal sensors in mammals, TRP channels appear to have an ancient heat-sensing function that is retained in both vertebrates and invertebrates. Given that this study has identified a heat-sensing role for norpA, and norpA is known to activate TRP channels in photoreception, it is not unreasonable to suppose that norpA plays a general role in responses to temperature stimuli (Collins, 2004).

per splicing levels may also impact on aspects of behavior other than the timing of evening locomotor activity. For instance, the free-running period of norpAP41 is ~1 h shorter than WT. The splicing levels of per mRNA are greatly elevated in this background, and elevated splicing is predicted to advance the Per protein cycle and thus speed up the clock. In fact, the splicing mechanism should have the effect of speeding up the clock at colder temperatures and slowing it down at high temperatures, thereby providing a potential basis for temperature compensation (Collins, 2004).

The position of the evening activity peak at different temperatures moves in different mutant backgrounds. For WT, norpAP41, and cryb, the level of splicing appears to correlate with the position of the evening activity peak at different temperatures. At 18°C, there is a small but significantly greater relative amount of spliced per RNA in cryb than in WT, resulting in the earlier evening activity peak seen in cryb flies. This difference in per splicing is greatest after lights off at both temperatures. This is when Per levels will be rising, because Tim is present for Per stabilization, so enhancement of Per accumulation by elevated per splicing is likely to have its most noticeable effect around dusk or early evening. A similarly consistent situation is seen in norpAP41: there is more spliced per mRNA present at 18°C (65%) than 29°C (55%), accounting for the earlier peak of evening activity at 18°C. Additionally these levels are higher than those seen in either WT (45% and 25% per transcripts spliced at each temperature) or cryb (55% and 40%) and relates to the earlier phases of locomotor activity seen in norpAP41 compared to the other genotypes. However, at 18°C there is more spliced per in norpAP41 than in cryb, but the evening activity peak occurs at the same time. The simplest explanation is that there is a limit to how early the evening activity peak can occur, no matter what the per splicing level, because splicing alters the accumulation of Per protein; this is limited by the light-dependent degradation of Tim. Therefore, in general, the level of splicing determines when the peak level of locomotor activity will occur (Collins, 2004).

The level of splicing of the per intron cannot be the only determinant of evening peak position, because the relationship between the per splicing level and evening activity peak position breaks down in norpAP41; cryb and gl60j, where there are different levels of splicing at the two temperatures but no corresponding difference in the evening peak position. When the underlying per mRNA cycles of gl60j, norpAP41, and WT flies were analyzed at 18°C and 29°C, it was found that whereas per levels cycle in norpAp41 and WT, this cycle is lost in gl60j. If there is no underlying per RNA cycle, then there is no mRNA peak to be advanced or delayed by splicing (Collins, 2004).

At the cellular level, although gl is not a clock component, when mutated, it eliminates a number of clock-expressing cells within the head, including the eyes, ocelli, Hofbauer-Buchner (H-B) eyelet, and the dorsal neuron 1 (DN1) cells. Despite this, the primary effect on the clock is to remove most of the visual entrainment pathway, but the clock in the key pacemaker cells of gl60j mutants must still be functional, because behavior still entrains to LD cycles and remains rhythmic in DD. It is significant that the crosstalk between different classes of clock cells is essential for the generation of robust behavioral rhythms. Thus loss of the overall per mRNA rhythm may be a consequence of disrupting this network in gl60j, and, while leaving the basic system intact, this affects the more subtle temperature-sensitive aspects of entrainment. A similar argument based on an interruption of the entrainment network can also be proposed to explain the corresponding results with norpAP41; cryb double mutants, because in this case per mRNA is assumed to be noncycling because of the cryb background. However, the locomotor behavior of cryb single mutants remains thermosensitive even though overall per mRNA is noncycling. Thus, only when the photoreceptive pathway and mRNA cycle are both compromised (as in gl and norpAP41; cryb) is locomotor behavior insensitive to temperature-dependent changes in per splicing levels (Collins, 2004).

A model is presented of how light and temperature may set the splicing level of the clock. How temperature is detected by the splicing machinery is not yet clear, but there is compelling evidence that norpA plays a role. At low temperatures, the splicing level is primarily set by light via the visual system rather than Cry, which is then remembered during the night. In longer periods of darkness such as in DD, this memory decays, and splicing levels begin to rise. Thus the visual system represses splicing by enhancing the effects of an unknown repressor molecule(s) that is sensitive to temperature change and the norpA PLC. At high temperatures, the regulation of splicing is more stringent and complex and recruits the circadian clock. Again, the light input received through the visual system sets the low splicing level during the day. This appears to also depend on the presence of at least two of the three molecules, Per, Tim, or Cry, because elimination of any one of these gives a barely detectable daytime rise in splicing, reflecting the very low levels of Per, Tim, and Cry at this time. However, elimination of both Per and Cry in the per01; cryb double mutant lifts all light-dependent repression during the day (Collins, 2004).

At night, the level of splicing set during the day by the visual system is again remembered and maintained by the clock at night. If per, tim, or cry is eliminated, then this repression of splicing is lost at night, generating the day/night difference in splicing levels. In gl60j cryb or norpAP41; cryb, because there is no visual light input during the day, there is no splicing level for the clock to remember, and therefore there is no day/night difference in splicing levels. Thus at high temperature, the visual system activates the repressor molecule during the day, and the clock maintains this activation at night. It is assumed that recruiting the clock at high temperature to inhibit per splicing is required to ensure that the fly's locomotor/foraging behavior is adaptive and does not encroach on those times of the day when there would be a significant risk of desiccation (Collins, 2004).

Temperature synchronization of the Drosophila circadian clock

Circadian clocks are synchronized by both light:dark cycles and by temperature fluctuations. Although it has long been known that temperature cycles can robustly entrain Drosophila locomotor rhythms, nothing is known about the molecular mechanisms involved. This study shows that temperature cycles induce synchronized behavioral rhythms and oscillations of the clock proteins Period and Timeless in constant light, a situation that normally leads to molecular and behavioral arrhythmicity. Expression of the Drosophila clock gene period can be entrained by temperature cycles in cultured body parts and isolated brains. The phospholipase C encoded by the norpA gene contributes to thermal entrainment, suggesting that a receptor-coupled transduction cascade signals temperature changes to the circadian clock. The further genetic dissection of temperature-entrainment was initiated, and the novel Drosophila mutation nocte was isolated. nocte mutants are defective in molecular and behavioral entrainment by temperature cycles but synchronizes normally to light:dark cycles. It is concluded that temperature synchronization of the circadian clock is a tissue-autonomous process that is able to override the arrhythmia-inducing effects of constant light. These data suggest that temperature synchronization involves a cell-autonomous signal-transduction cascade from a thermal receptor to the circadian clock. This process includes the function of phospholipase C and the product specified by the novel mutation nocte (Glaser, 2005).

Although it has been known for a long time that temperature can serve as a potent Zeitgeber to entrain circadian rhythms in animals, practically nothing was known about thermal-entrainment mechanisms and, thus, about the genes and molecules involved. This study has revealed that temperature entrainment of clock-protein expression can function at the level of isolated tissues, independent of the antennal thermosensors studied with regard to Drosophila's acute thermal responsiveness described earlier. The situation is therefore similar to that of circadian photoreception in flies: Clock-gene-expressing tissues can be synchronized in the absence of external, image-forming photoreceptors, and this synchronization is probably mediated by the blue-light photoreceptor Cryptochrome. Similarly, these findings suggest the existence of a cell-autonomous thermoreceptor dedicated to temperature entrainment of the circadian clock. Among the candidates for such a receptor are the transient receptor potential vanilloid (TRPV) channels that have been shown to function in thermoreception in mammals and fly larvae (Glaser, 2005).

The nocte mutant was isolated in a novel screen for temperature-entrainment variants; nocte specifically affects synchronization of the circadian clock to this Zeitgeber (namely, temperature cycles). Such mutant flies are drastically impaired in molecular entrainment of Per-LUC reporter-gene rhythms as well as those of native Per and Tim expression. Behavioral rhythms can be entrained by light:dark, but not by temperature cycles, in nocte flies. Moreover, nocte flies do not affect circadian clock function as such because mutant flies are robustly rhythmic in constant darkness. The circadian clock of nocte flies is also properly temperature compensated; their free running period does not change as a function of increasing or decreasing constant ambient temperatures. These findings show that the assumed product of this gene plays a central role in, and is specific for, temperature entrainment (Glaser, 2005).

It has been shown that the norpA gene is involved in the light-entrainment pathway that ends at the brain's clock. The phospholipase C (PLC) encoded by this gene is an essential factor of the canonical photo-transduction cascade within Drosophila's external photoreceptors. Loss-of-function norpA mutations (such as norpAP24 and norpAP41, as applied in this study) disrupt this pathway and cause visual blindness -- but they also blind the eyes' contribution to circadian entrainment by light (Glaser, 2005).

In addition, norpA contributes to a temperature-sensitive splicing event at the 3' end of the per gene. Splicing of a per intron is enhanced by relatively cold temperatures, and this enhancement leads to an earlier increase of per mRNA during the daily cycle of per RNA accumulation and decline (Majercak, 1999; Majercak, 2004). Correlated with this early upswing is an advanced behavioral activity peak in cold conditions. Because both phenomena are enhanced by shortened photoperiods and suppressed by long photoperiods, it was suggested that the 3' alternative splicing event serves as a mechanism to adjust the fly's behavior to seasonal changes: More locomotion during the day in the winter, with its short photoperiods, and more behavior in the evening during the summer, to avoid the desiccation effects of midday heat (Glaser, 2005).

But are norpA and the 3'splicing mechanism also important for the more basic features of day-by-day temperature entrainment? The answer, from this analysis, is yes and no: PLC is clearly involved because norpA mutations affect both molecular and behavioral entrainment to temperature cycles. This is not true for the alternative splicing event at per's 3' end: Two types of controls (wild-type and y w) robustly synchronized their behavioral rhythms to temperature cycles in constant light and constitutively expressed roughly equal amounts of the spliced and unspliced versions of per RNA in the same LL and temperature-cycling conditions. Therefore, temporal regulation of the 3' splicing event is not necessary for entrainment to temperature cycles (Glaser, 2005).

The idea is favored that the PLC encoded by norpA has an additional role to its known functions in photo transduction and thermal regulation of splicing. It is possible that a signal-transduction cascade, similar to the visual one operating in the compound eye, is used to transduce the temperature signal to the clock. It is not known whether all clock-gene-expressing tissues also express norpA (although it is notable that norpA is expressed in adult tissues way beyond the external eyes. If not, this could explain why the temperature-entrainment defects in norpA mutants in behavior seem less severe than those of nocte. norpA's function in certain tissues could be replaced by other PLC enzymes encoded by different genes. In this respect, one of the more salient norpA mutant defects that was uncovered, that such flies cannot entrain Per-LUC rhythms to temperature cycles, suggests that the temperature-entrainment pathway involves a receptor-coupled signal-transduction cascade that includes a crucial function for PLC (Glaser, 2005).

Robust temperature-entrained reporter-gene rhythms were observed only in transgenic situations in which two-thirds or the entirety of the Per protein was fused to luciferase. These results suggest that the temperature-entrainment mechanism targets clock proteins (at least Per) and does not rely on transcriptional mechanisms. Interestingly, in Neurospora, temperature entrainment is also mainly regulated at the protein level. This supposition is also supported by the surprisingly robust Per and Tim cyclings observed in fly heads under constant light and temperature cycling conditions. These protein oscillations were severely damped in the temperature-entrainment-defective nocte mutant (Glaser, 2005).

Previous work showed that heat pulses of 37°C can induce stable molecular and behavioral phase shifts when applied during the early night but not during the late night. These heat pulses function at the posttranscriptional level because they result in rapid disappearance of Per and Tim. Nevertheless, responsiveness of the clock to heat pulses seems to be mediated by a different mechanism, when compared with daily entrainment analyzed in the current study, because heat pulses involving elevated temperatures below 37°C (i.e., 31°C and 28°C) did not lead to significant clock-protein degradation, whereas temperature cycles applied in the current study (which were in a physiological range, 17°C to 25°C) did cause fluctuations in protein concentrations (Glaser, 2005).

A surprising finding in this study was that temperature-entrained molecular oscillations of Per-LUC and of endogenous Per and Tim proteins are robust in constant light. It was reported earlier that upon transfer to constant light and temperature, Tim protein is expressed at constitutively low levels -- probably by CRY-mediated light absorption followed by Tim:CRY interaction. Per protein continues to oscillate for about 2.5 days after transfer to LL, after which its expression levels also becomes low and constitutive. In the current experiments, Per and Tim still oscillated after 4 days in LL when temperatures were cycling, and Per-LUC luminescence oscillations continued with robust amplitude for more than 5 days. These results clearly show that temperature cycles override the arrhythmia-inducing effects of constant light and explain why circadian entrainment of behavioral and physiological rhythmicity is observed under these conditions (Glaser, 2005).

Future work will illuminate which molecules mediate temperature entrainment in addition to phospholipase C. Given the drastic and specific effects of the nocte mutation on temperature entrainment, the factor encoded by this gene will almost certainly be revealed to play a central role in this process (Glaser, 2005).

This study has shown that temperature cycles induce molecular rhythms of clock-gene expression, even in the presence of constant light, which normally results in complete molecular and behavioral arrhythmia. Synchronization was observed in isolated peripheral clock tissues and in the brain, demonstrating that the process is tissue autonomous and is responsible for the synchronized locomotor behavior under constant-light and temperature-cycling conditions. The data suggest that the mechanism functions at a posttranscriptional level involving at least the clock protein Per. Phospholipase C is likely to be involved in the signaling mechanism from the thermal receptor to the clock. The novel mutation nocte specifies a factor that is specific for thermal synchronization of the circadian clock in flies, demonstrating that this input pathway can be genetically dissected, as has been similarly shown for the light input into the circadian clock (Glaser, 2005).

DAG lipase activity is necessary for TRP channel regulation in Drosophila photoreceptors

In Drosophila, a phospholipase C-mediated signaling cascade links photoexcitation of rhodopsin to the opening of the TRP/TRPL channels. A lipid product of the cascade, diacylglycerol (DAG) and its metabolite(s), polyunsaturated fatty acids (PUFAs), have both been proposed as potential excitatory messengers. A crucial enzyme in the understanding of this process is likely to be DAG lipase (DAGL). However, DAGLs that might fulfill this role have not been previously identified in any organism. In this work, the Drosophila DAGL gene, inaE, has been identified from mutants that are defective in photoreceptor responses to light. The inaE-encoded protein isoforms show high sequence similarity to known mammalian DAG lipases, exhibit DAG lipase activity in vitro, and are highly expressed in photoreceptors. Analyses of norpA inaE double mutants and severe inaE mutants show that normal DAGL activity is required for the generation of physiologically meaningful photoreceptor responses (Leung, 2008).

Visual transduction in Drosophila utilizes a G protein-coupled, phospholipase C-mediated signaling cascade. Phospholipase C, upon activation via rhodopsin and G protein, Gq, catalyzes the hydrolysis of phosphatidylinositol 4,5-bisphosphate (PIP2) into two potential second messengers, diacylglycerol (DAG) and inositol trisphosphate (IP3). A body of evidence suggests that IP3 is not involved in Drosophila phototransduction, leaving the DAG branch as a likely source of messenger(s) of activation for the phototransduction channels, transient receptor potential (TRP) and TRP-like (TRPL). The mechanism by which the diacylglycerol (DAG) branch might activate the TRP/TRPL channels is still unresolved. The first indication that a lipid messenger might be involved was provided by Chyb (1999), who showed that polyunsaturated fatty acids (PUFAs) could activate both TRP and TRPL channels either in intact photoreceptors or heterologous expression systems. Later, evidence was provided that DAG is required for photoreceptor excitation using DAG kinase mutants, rdgA. Because the conversion of DAG to phosphatidic acid is blocked in these mutants, they should have an elevated DAG basal level. TRP/TRPL channels are constitutively active in rdgA, and diminished responses of hypomorphic PLC (norpA) mutants can be greatly enhanced by rdgA mutations, in support of the contention that DAG might be excitatory to the channels. However, rdgA mutations are expected to raise the basal levels of not only DAG but also its metabolites. In addition to these two molecules, phosphatidylinositol 4,5-bisphosphate (PIP2) has also been suggested to play a role in channel excitation. Currently, no consensus exists as to which, if any, of these might be the excitatory agent for TRP/TRPL channels (Leung, 2008).

Drosophila TRP is the founding member of a superfamily of TRP channel proteins. There are now nearly 30 mammalian members of this superfamily comprising seven subfamilies. Although these channels are heterogeneous in their modes of activation, at least four mammalian TRP channels have been reported to be activated by DAG: TRPC2, -3, -6, and -7. While there may be variations in the mechanisms of activation of these channels, elucidation of Drosophila TRP/TRPL channel activation could provide insight into activation of these channels as well (Leung, 2008).

Because both DAG and its potential metabolite, PUFA, have been implicated in the activation of TRP/TRPL channels, a key enzyme in this process is likely to be DAG lipase, which catalyzes the hydrolysis of DAG. Little is known about DAG lipases. Two mammalian DAG lipase genes, DAGLα and -β, have been identified by a bioinformatics approach and characterized both biochemically and molecularly), and many proteins homologous to DAGα and -β have been identified across species. In the case of Drosophila, , rolling blackout (rbo) has been suggested to be in a DAG lipase gene. The protein encoded by the rbo gene, however, shows little homology to the known mammalian DAG lipases. Moreover, conditional loss of the RBO protein leads to rapid depletion of DAG, the opposite of what one would expect if RBO catalyzes the hydrolysis of DAG. Furthermore, in the absence of previous activity, the receptor potential is normal in rbo mutants, making it unlikely that RBO has any direct involvement in the activation of TRP/TRPL channels. Other than rbo, no candidate DAG lipase that might function in phototransduction has been reported in any species (Leung, 2008).

This work reports on a Drosophila DAG lipase (DAGL) gene, inaE, identified from mutants that are defective in photoreceptor responses to light. The protein isoforms encoded by this gene show high sequence similarity to the two known mammalian DAGLs, exhibit DAGL activity in vitro, are highly expressed in photoreceptors, and have access to rhabdomeres. Genetic evidence suggests that the inaE-encoded DAGLs interact in vivo with the DAG generated in the phototransduction cascade. Analysis of mutants generated by imprecise excision of P element insertion in inaE show that no physiologically meaningful photoreceptor responses can be generated if inaE gene is severely impaired (Leung, 2008).

The inaE gene was identified by two ethylmethane sulfonate (EMS)-induced allelic mutants: N125 and P19. These mutants are characterized by their 'ina' (inactivation, no afterpotential) electroretinogram (ERG) phenotype. Wild-type flies, when placed on a white-eye (w) background, respond to a bright blue stimulus with a large response during light stimulus followed by a prolonged depolarizing afterpotential (PDA) after the light is turned off. A second blue stimulus elicits only a small response, originating from R7/8 photoreceptors, superposed on the PDA. By contrast, in ina mutants, the response begins to decay during stimulus (inactivation), and the decay continues after the stimulus. As a result, the PDA is greatly diminished in amplitude (no afterpotential). This phenotype can also be viewed as a mild form of the 'trp' phenotype displayed by strong mutants of the TRP channel gene. In trp mutants, the response to the first blue stimulus decays nearly to baseline during stimulus, and there is no PDA (Leung, 2008).

Moreover, responses of inaE mutants resemble those of trp in that they both display refractory properties. Following a response to the first stimulus, only very small responses can be elicited from trp until they recover over a period of minutes, while wild-type responses recover almost immediately. Likewise, inaE mutants exhibit a similar refractory period, although the degree and duration of response suppression are not as pronounced or prolonged as in trp (Leung, 2008).

In addition to the above similarities, inaEN125 acts as a genetic enhancer of TrpP365. TrpP365 is a semidominant allele of trp, which causes constitutive activation of TRP channels and, as a result, massive photoreceptor degeneration from excessive Ca2+ influx. In TrpP365 homozygotes, degeneration is already so advanced in 1- to 2-day-old flies that essentially no ERGs can be elicited. TrpP365 heterozygotes exhibit a much milder phenotype and elicit ERGs of substantial amplitude at the same age. However, if inaEN125 is introduced into the TrpP365/+ background, the resulting phenotype is as severe as that of TrpP365 homozygotes. The genetic enhancement of TrpP365/+ by inaEN125 and the basic similarity of ERG phenotypes between inaE and trp mutants led to the hypothesis that the protein products of these two genes may interact and/or subserve closely related functions (Leung, 2008).

The CG33174 gene had not been characterized previously, and its function was electronically inferred as 'triacylglycerol lipase (TAGL) activity'. However, the possibility is considered that the above annotation could simply reflect a dearth of information on DAGLs. The first two human DAGLs, DAGLα and -β, were cloned and characterized by a bioinformatic approach and shown to be sn-1 type DAGLs. Multiple alignment of INAE-A and INAE-D with DAGLα and -β revealed extensive sequence and domain conservations. All four proteins are predicted to have four transmembrane segments near the N-terminal region, and they all have a lipase_3 domain with a highly conserved serine active site. Overall sequence homology between INAE-D and the two human DAGLs is 39% identity and 56% similarity for DAGLα and 30% identity and 50% similarity for DAGLβ, respectively. In the lipase_3 domain, the sequence homology between INAE-A/D and the mammalian proteins rises to 60% and 45% identity and 73% and 63% similarity for DAGLα and DAGLβ, respectively (Leung, 2008).

To demonstrate that the INAE proteins have DAG lipase activity, the INAE-A and -D protein isoforms were expressed in E. coli and purified to >95% purity to carry out DAG lipase assays using 1-stearoyl-2-arachidonoyl-sn-glycerol as substrate, and the lipase assay products were analyzed by liquid chromatography-mass spectrometry (LC-MS) and gas chromatography-mass spectrometry (GC-MS) for identification of hydrolysis products and kinetic studies (Leung, 2008).

LC-MS detected four products from the analysis of both INAE isoforms: two primary products, stearic acid (18:0) and 2-arachidonoyl glycerol (2-AG), and two minor products, arachidonic acid (20:4) and 1-stearoyl glycerol (1-SG), eluting at 6.3, 9.3, 5.8, and 8.7 min, respectively. Two primary products corresponded to hydrolysis at the sn-1 position of DAG substrate, and the two minor products corresponded to hydrolysis at the sn-2 position. Thus, in vitro, the two recombinant INAE isoforms are both DAG lipases highly preferential for hydrolysis at the sn-1 position, with the D form having much higher activity than the A form (Leung, 2008).

A growing body of evidence suggests that Drosophila phototransduction utilizes the DAG branch of the G protein-coupled, PLCβ-mediated signaling pathway). Although DAG lipase is expected to play a critical role in this pathway, no DAG lipase that could play such a role had been identified previously in Drosophila. This study reports on a DAG lipase identified from the Drosophila mutants, inaE. The inaE gene was found to encode two protein isoforms, INAE-A and INAE-D, by alternative splicing. Both of these proteins are highly homologous to the two previously identified mammalian sn-1 type DAG lipases, and in vitro DAG lipase assays of recombinant INAE-A and INAE-D showed that both are DAG lipases highly preferential for hydrolysis at the sn-1 position. Expression of the INAE protein is not restricted to the eye but occurs throughout the head, consistent with the finding that strong mutations in this gene are homozygous lethal. In photoreceptors, anti-INAE antibody labeling occurs as punctate staining scattered throughout the photoreceptor cytoplasm. Occasionally, some of the puncta are found within the rhabdomeres, indicating that some DAGL enters the rhabdomeres. Results of the norpA inaE double mutant study provide strong functional support for the above observation. In this study, the receptor potential disappears in an inaE allele-dependent manner -- the stronger the inaE allele in the double mutant, the more severe the double mutant phenotype. The allele dependence strongly suggests that the action of inaE-encoded DAGL is responsible for the observed double mutant phenotype. Furthermore, to affect the receptor potential phenotype, DAGL must act on the DAG generated by norpA-encoded PLCβ, and, for that to occur, DAGL must enter the rhabdomeres (Leung, 2008).

Because inaE mutations already available were all relatively mild, severe mutations were generated by imprecise excisions of a P element insertion in the inaE gene. These imprecise excision alleles were homozygous lethal and had to be studied as eye mosaics. Quantitative RT-PCR results showed that even the severest of these imprecise excision mutants, inaExl18, is not a null mutant and expresses RNA at ~25% of the normal level. This mutation profoundly affects the photoreceptor responses to light. If xl18 is placed on a norpAH43 background to reduce the amount of DAG generated, the light stimulus generates no response at all. In xl18 flies themselves, a bright prolonged stimulus generates only a small response of slow kinetics that decays to baseline completely during the stimulus. This response most likely represents the residual DAGL activity in this severely affected mutant. As the severity of mutation progressively decreases in the xl series of mutants, the receptor potential phenotype returns to normal in an allele-dependent manner. Again, the inaE allele dependence strongly argues that the action of inaE-encoded DAGL is responsible for the observed change in the receptor potential phenotype. These results, taken together, suggest (1) that the production of DAG metabolite(s) through the action of the inaE-encoded DAGL is required for the generation of photoreceptor responses to light and (2) that, in the absence of the metabolite, DAG plays little direct role in the activation of channels. However, the identity of the excitatory molecule cannot be specified from this work. It could be one or more of the products generated by INAE, such as monoacylglycerol (2-AG) or stearic acid or even DAGL (INAE) itself (Leung, 2008).

While DAG may not have a direct role in channel activation, evidence was found suggesting that it may be important in regulating the action of the DAG metabolite that acts as an excitatory agent, although the evidence is still largely indirect. The ability of inaEN125 to act as an enhancer of TrpP365/+ seems to present a quandary when considered in relation to the results summarized above. If DAG has little or no direct role in channel activation, how does one explain the disappearance of the small response present in P365/+ when N125 is added to this background? A simple explanation for the phenomenon would be that DAG is excitatory to the channels and that adding N125 to the P365/+ background raised the level of DAG to make more channels to become constitutively active in N125;P365/+ than in P365/+. However, results of the experiment replacing N125 with a stronger inaE allele, xl18, in the N125;P365/+ double mutant run counter to this simple explanation. Replacing N125 with xl18 should have sharply raised the basal DAG level further in the double mutant. If DAG were excitatory, the resting potential should have depolarized even more than before the N125 replacement, and no receptor potential at all should have been obtained. Just the opposite results were obtained. A small but distinct receptor potential could be recorded from xl18;P365/+, and the resting potential has returned to the level in P365/+. These results are incompatible with the hypothesis that DAG is excitatory to the channel and instead provide another line of evidence for the conclusions summarized earlier (Leung, 2008).

However, the fact that a much more severe phenotype is obtained in N125;P365/+ than in P365/+ or xl18;P365/+ suggests that DAG may have a role in facilitating, enhancing, and orchestrating the action of the DAG metabolite that serves as the excitatory agent. This action of DAG would be more noticeable under conditions in which a sufficient amount of the excitatory product is produced, as in N125;P365/+ rather than in xl18;P365/+. A similar action of DAG can also be inferred from the norpA inaE double mutant studies. In this series of experiments, hypomorphic norpA mutation, H43, was used to restrict the amount of DAG generated both in the single and double mutants. The response obtained from H43 N125 is short in duration but has nearly the same maximum amplitude as the H43 response and much faster time course of rise than the H43 response. The shortness of response duration may be due to the fact that, under the conditions of this experiment (restricted DAG generation), the response cannot be sustained during a bright prolonged stimulus. This response arises as a result of DAGL activity because further reducing the DAGL activity (xl18 mutation) abolishes the response. However, the fact that adding N125 to the H43 background resulted in a response of faster time course may also be a manifestation of the enhancing and facilitatory effects of DAG on the excitatory agent. Speculating further, the facilitatory action of DAG might be in place to ensure that the excitation of channels is light regulated, because DAGL activity is not light regulated while the generation of DAG is (Leung, 2008).


EVOLUTIONARY HOMOLOGS

To know whether or not the set of genes involved in the inositol phospholipid signaling pathway already existed in the early evolution of animals, phospholipase Cs (PLCs) were cloned from Ephydatia fluviatilis (freshwater sponge) and Hydra magnipapillata strain 105 (hydra). Two PLC cDNAs, PLC-betaS and PLC-gammaS, were cloned from sponge and three cDNAs, PLC-betaH1, PLC-betaH2, and PLC-deltaH, from hydra. From the domain organization and the divergence pattern in the PLC family tree, the sponge PLC-betaS and PLC-gammaS and the hydra PLC-deltaH are possibly homologous to the vertebrate PLC-beta, PLC-gamma and PLC-delta subtypes, respectively. A detailed phylogenetic analysis suggests that the hydra PLC-betaH1 and PLC-betaH2 are homologs of the vertebrate PLC-beta1/2/3/Drosophila PLC21 and the vertebrate PLC-beta4/Drosophila norpA, respectively. A phylogenetic analysis of the PLC family and the protein kinase C (PKC) family, together with that of the G protein alpha subunit (Galpha) family, reveals that the origin of the set of genes G(alpha)q, PLC, PKC involved in the inositol phospholipid signaling pathway is very old, going back to dates before the parazoan-eumetazoan split, the earliest branching among extant animal phyla (Koyanagi, 1998).

The rpa (receptor potential absent) mutation of the blowfly, Calliphora erythrocephala, reduces the light-evoked responses of photoreceptor cells and renders the fly blind. This phenotype is similar to the phenotype caused by norpA mutations in Drosophila which have been shown to occur within a gene encoding phospholipase C. In Western blots, norpA antiserum stains a protein in homogenates of wild-type Calliphora eye and head that is similar in molecular weight to the NorpA protein. Very little staining of this protein is observed in similar homogenates of rpa mutant. Moreover, NorpA antiserum strongly stains retina in immunohistochemical assays of wild-type adult head, but not in rpa mutant. Furthermore, eyes of rpa mutant have a reduced amount of phospholipase C activity compared to eye of wild-type Calliphora. These data suggest that the rpa mutation occurs in a phospholipase C gene of the blowfly that is homologous to the norpA gene of Drosophila (McKay, 1994a).

Invertebrate visual signal transduction is initiated by rhodopsin activation of a guanine nucleotide binding protein, Gq, which stimulates phospholipase C (PLC) activity. A 140-kDa PLC enzyme has been purified from squid photoreceptors that is regulated by squid Gq. In these studies, an additional PLC enzyme was purified from the cytosol of squid photoreceptors and identified as a 70-kDa protein by SDS-polyacrylamide gel electrophoresis. Hydrolysis of phosphatidylinositol 4,5-bisphosphate (PIP2) by PLC-70 is optimal at pH 5 in the presence of 100 microM Ca2+ with a specific activity of 10.3 micromol min-1 mg-1. A polyclonal antibody raised against purified PLC-70 does not recognize purified PLC-140, and proteolytic digestion of the two purified enzymes with trypsin or Staphylococcus aureaus V8 protease shows distinct patterns of peptide fragments, indicating that PLC-70 is not a fragment of PLC-140. The partial amino acid sequence of the protein shows homology with PLC21 and norpA isozymes cloned from Drosophila, and mammalian PLC beta isozymes. Reconstitution of purified GTPgammaS-bound soluble squid Gq with PLC-70 results in significant enhancement of PIP2 hydrolysis over a range of Ca2+ concentrations and shifts the maximum activation by calcium to 1 microM. These results suggest that cephalopod phototransduction is mediated by Gq activation of more than one cytosolic PLC enzyme (Mitchell, 1998).

Conserved regions of norpA cDNA were used to isolate bovine cDNAs. These encode four alternative forms of phospholipase C of the beta class that are highly homologous to the NorpA protein and expressed preferentially in the retina. Two of the variants are highly unusual in that they lack much of the N-terminal region present in all other known phospholipases C. The sequence conservation between these proteins and the NorpA protein is higher than that between any other known phospholipases C. GTPase sequence motifs found in proteins of the GTPase superfamily are found conserved in all four variants of the bovine retinal protein as well as the NorpA protein but not in other phospholipases C. Results suggest that these proteins together with the NorpA protein constitute a distinctive subfamily of phospholipases C that are closely related in structure, function, and tissue distribution. Mutations in the NorpA gene, in addition to blocking phototransduction, cause light-dependent degeneration of photoreceptors. In view of the strong similarity in structure and tissue distribution, a defect in these proteins may have similar consequences in the mammalian retina (Ferreira, 1993).

Inositol phospholipid-specific phospholipase C (PLC) isozymes in bovine retina have been characterized . Chromatography of a retinal homogenate on a heparin column partially resolves six peaks of PLC activity, which differ in their relative selectivities for the substrates phosphatidyl 4,5-bisphosphate (PIP2) and phosphatidylinositol (PI). Five of the peaks correspond to the known PLC isozymes PLC-beta 1, PLC-beta 3, PLC-gamma 1, PLC-delta 1, and PLC-delta 2. PLC-beta 1, PLC-beta 3, PLC-gamma 1, and PLC-delta 1 in the retinal fractions were identified by immunoblotting with isozyme-specific antibodies, and PLC-delta 2 was identified by direct sequencing of tryptic peptides. PLC-gamma 2 and PLC-beta 2 were not detectable by immunoblot analysis. In addition to five of the seven mammalian PLC isozymes identified to date, bovine retina contained a previously unidentified PLC, which exhibited the highest selectivity for PIP2 over PI. The new PLC was purified from a retinal particulate fraction to yield a preparation that contained a major protein band with an apparent molecular mass of 130 kDa on SDS-polyacrylamide gels. Sequence analysis of 12 tryptic peptides derived from the 130-kDa protein suggested that the primary structure of the new PLC is similar to those members of beta-type PLC isozymes, especially to that of PLC-norpA, which was originally identified in Drosophila eye. The new enzyme was thus named PLC-beta 4. A search of a rat brain cDNA library with the polymerase chain reaction and oligonucleotide primers based on common PLC amino acid sequences resulted in the cloning of a rat brain cDNA corresponding to a previously uncharacterized PLC. The cDNA encodes a putative polypeptide of 1176 amino acids, with a calculated molecular mass of 134,532 daltons, that contains the sequences of all 12 tryptic peptides of PLC-beta 4. Furthermore, the deduced amino acid sequence of the encoded protein is more related to PLC-norpA than to any of the three mammalian PLC-beta isozymes. These results suggest that the brain cDNA encodes PLC-beta 4, which is likely a mammalian homolog of PLC-norpA (Lee, 1993).

Phospholipase C-beta 4(PLC-beta 4), a new member of phospholipase C isozyme, was purified from bovine cerebellum. The cDNA encoding rat PLC-beta 4 has been cloned from a cDNA library prepared from rat brain. The predicted open reading frame encodes a protein of 1,176 amino acids with a calculated molecular weight of 134,552. The deduced amino acid sequence exhibits 39, 36, and 36% identity with the sequences of rat PLC-beta 1, human PLC-beta 2, and rat PLC-beta 3, respectively. The amino acid sequence of PLC-beta 4, especially, shows higher identity (50%) with norpA PLC sequence from Drosophila melanogaster than those of other PLC-beta subtypes, suggesting that the PLC-beta 4 might be a mammalian PLC equivalent of norpA PLC implicated in photosignal transduction in Drosophila (Kim, 1993).

Transient transfection assays were used to determine how the activity of phospholipase C beta 4, which is preferentially expressed in retina, is regulated. An expression vector carrying the full-length cDNA corresponding to phospholipase C beta 4 was constructed and co-transfected into COS-7 cells together with cDNA encoding the alpha subunits of the Gq class and various beta and gamma subunits corresponding to the heterotrimeric GTP-binding proteins. All the alpha subunits of the Gq class, including G alpha q, G alpha 11, G alpha 14, G alpha 15, and G alpha 16 can activate PLC beta 4 and none of the G beta gamma subunits tested, including G beta 1 gamma 1, G beta 1 gamma 2, G beta 1 gamma 3, or G beta 2 gamma 2, activate phospholipase C beta 4. In control experiments, cotransfection with cDNA encoding the alpha subunit of transducin or Gi2 gives no activation of PLC beta 4. These results indicate that phospholipase C beta 4 is activated by G alpha subunits that are members of the Gq class, and, like the phospholipase C beta 1 isoform, it is refractory to activation in the transfection assay by many of the combinations of beta and gamma subunits found in the heterotrimeric G-proteins (Jiang, 1994).

PLC-beta 4 has now been shown to differ from the other three mammalian beta-type isozymes (PLC-beta 1, -beta 2, and -beta 3) in that it is selectively inhibited by ribonucleotides. The inhibition requires the 5'-phosphate and 2'-hydroxyl groups of ribose as well as the base moiety. Thus, deoxyribonucleotides and ribose 5-phosphate are not inhibitory. The monophosphate, diphosphate, and triphosphate nucleoside derivatives are all inhibitory, whereas cyclic nucleotides are ineffective. Purine nucleotides are more potent inhibitors than pyrimidine nucleotides. Unlike the other beta-type isozymes, PLC-beta 4 contains the GX4GKS consensus sequence for the recognition of the phosphoryl group of nucleotides. In the absence of ribonucleotides, the specific activity of PLC-beta 4 toward phosphatidyl-inositol 4,5-bisphosphate is four to five times the average specific activity of PLC-beta 1 and PLC-beta 3. Thus, nucleotide-dependent inhibition may serve to reduce the activity of PLC-beta 4 in the absence of a hormonal signal. The regulation of PLC-beta 4 by G-proteins was also studied. Similar to the other three PLC-beta isozymes, PLC-beta 4 is activated by the alpha subunit of Gq but not by the transducin alpha subunit. However, unlike other PLC-beta isozymes, PLC-beta 4 was not responsive to activation by G beta gamma subunits (C. W. Lee, 1994).

The Drosophila norpA gene encodes a phosphatidylinositol-specific phospholipase C (PI-PLC) expressed predominantly in photoreceptors and involved in phototransduction. However, no direct role for a phospholipase C in vertebrate phototransduction has been identified to date. Bovine cDNAs encoding PI-PLC isoforms expressed predominantly in the retina have been isolated and characterized. These isoforms have higher homology to the NorpA protein than to any other known PI-PLC. Evidence is presented that the NorpA-homologous bovine retinal PI-PLCs, although found in other retinal neurons as well, are found in cones but not in rods. The results suggest that the phototransduction cascade in cones may utilize phospholipase C in addition to phosphodiesterase (Ferreira, 1994).

Inositol phospholipid-specific phospholipase C (PLC) generates two important second messengers, inositol triphosphate and diacylglycerol. Rat PLC beta 4 cDNA is highly homologous to the norpA cDNA of Drosophila. PLC beta 4 gene expression has been mapped in rat brain tissue sections by in situ hybridization. The PLC beta 4 gene is expressed at high abundance in cerebellar Purkinje cells and neurones of the substantia nigra, the median geniculate bodies and the thalamic nuclei. PLC beta 4 transcripts are also detected in the mammillary nuclei, the neocortex, the habenula and the olfactory bulbs. The specific pattern of gene expression should help to clarify the relationships between the PLC beta 4 and various constituents of second-messenger systems involved in transduction mechanisms triggered by the stimulation of seven transmembrane domain receptors. The strong gene expression in Purkinje cells and retinal neurones suggests that PLC beta 4 may be involved in the pathogenesis of mouse and human neurological diseases characterized by ataxia and retinal degeneration (Roustan, 1995).

Defects in the Drosophila norpA gene encoding a phosphoinositide-specific phospholipase C (PLC) block invertebrate phototransduction and lead to retinal degeneration. The mammalian homolog, PLCB4, is expressed in rat brain, bovine cerebellum, and the bovine retina in several splice variants. To determine a possible role of PLCB4 gene defects in human disease, several overlapping cDNA clones were isolated from a human retina library. The composite cDNA sequence predicts a human PLC beta 4 polypeptide of 1022 amino acid residues (MW 117,000). This PLC beta 4 variant lacks a 165-amino-acid N-terminal domain characteristic for the rat brain isoforms, but has a distinct putative exon 1 unique for human and bovine retina isoforms. A PLC beta 4 monospecific antibody detects a major (130 kDa) and a minor (160 kDa) isoform in retina homogenates. Somatic cell hybrids and deletion panels were used to localize the PCLB4 gene to the short arm of chromosome 20. The gene was further sublocalized to 20p12 by fluorescence in situ hybridization (Alvarez, 1995).

Expression of G protein-regulated phospholipase C (PLC) beta 4 in the retina, lateral geniculate nucleus, and superior colliculus implies that PLC beta 4 may play a role in the mammalian visual process. A mouse line that lacks PLC beta 4 was generated and the physiological significance of PLC beta 4 in murine visual function was investigated. Behavioral tests using a shuttle box demonstrated that the mice lacking PLC beta 4 are impaired in their visual processing abilities, whereas they showed no deficit in their auditory abilities. In addition, the PLC beta 4-null mice show 4-fold reduction in the maximal amplitude of the rod a- and b-wave components of their electroretinograms relative to their littermate controls. However, recording from single rod photoreceptors did not reveal any significant differences between the PLC beta 4-null and wild-type littermates, nor were there any apparent differences in retinas examined with light microscopy. While the behavioral and electroretinographic results indicate that PLC beta 4 plays a significant role in mammalian visual signal processing, isolated rod recording shows little or no apparent deficit, suggesting that the effect of PLC beta 4 deficiency on the rod signaling pathway occurs at some stage after the initial phototransduction cascade and may require cell-cell interactions between rods and other retinal cells (Jiang, 1996).

A variety of extracellular signals are transduced across the cell membrane by the enzyme phosphoinositide-specific phospholipase C-beta (PLC-beta) coupled with guanine-nucleotide-binding G proteins. There are four isoenzymes of PLC-beta, beta1-beta4, but their functions in vivo are not known. The roles of PLC-beta1 and PLC-beta4 in the brain were examined by generating null mutations in mice: PLCbeta1-/- mice developed epilepsy and PLCbeta4-/- mice showed ataxia. The molecular basis of these phenotypes were determined. PLC-beta1 is involved in signal transduction in the cerebral cortex and hippocampus by coupling predominantly to the muscarinic acetylcholine receptor, whereas PLC-beta4 works through the metabotropic glutamate receptor in the cerebellum, illustrating how PLC-beta isoenzymes are used to generate different functions in the brain (Kim, 1997).

Phospholipase C (PLC)-beta4 has been considered to be a mammalian homolog of the NorpA PLC, which is responsible for visual signal transduction in Drosophila. A splice variant of PLC-beta4, PLC-beta4b, is identical to the 130-kDa PLC-beta4 (PLC-beta4a) except that the carboxyl-terminal 162 amino acids of PLC-beta4a are replaced by 10 distinct amino acids. The existence of PLC-beta4b transcripts in the rat brain was demonstrated by reverse transcription-polymerase chain reaction analysis. Immunological analysis using polyclonal antibody specific for PLC-beta4b reveals that this splice variant exists in rat brain cytosol. To investigate functional differences between the two forms of PLC-beta4, transient expression studies in COS-7 cells were conducted. PLC-beta4a is localized mainly in the particulate fraction of the cell, and it can be activated by Galphaq, whereas PLC-beta4b is localized exclusively in the soluble fraction, and it can not be activated by Galphaq. In addition, both PLC-beta4a and PLC-beta4b are not activated by G-protein betagamma-subunits purified from rat brain. These results suggest that PLC-beta4b may be regulated by a mechanism different from that of PLC-beta4a, and therefore it may play a distinct role in PLC-mediated signal transduction (Kim, 1998).


REFERENCES

Search PubMed for articles about Drosophila no receptor potential A

Adamski, F. M., et al. (1998). Interaction of eye protein kinase C and INAD in Drosophila. Localization of binding domains and electrophysiological characterization of a loss of association in transgenic flies. J. Biol. Chem. 273(28): 17713-9. PubMed Citation: 9651370

Alloway, P. G., Howard, L. and Dolph, P. J. (2000). The formation of stable rhodopsin-arrestin complexes induces apoptosis and photoreceptor cell degeneration. Neuron 28: 129-138. 11086989

Alvarez, R. A., et al. (1995). cDNA sequence and gene locus of the human retinal phosphoinositide-specific phospholipase-C beta 4 (PLCB4). Genomics 29(1): 53-61. PubMed Citation: 8530101

Alvarez, C. E., Robison, K. and Gilbert, W. (1996). Novel Gq alpha isoform is a candidate transducer of rhodopsin signaling in a Drosophila testes-autonomous pacemaker. Proc. Natl. Acad. Sci. 93(22): 12278-82. PubMed Citation: 8901571

Bloomquist, B. T., et al. (1988). Isolation of a putative phospholipase C gene of Drosophila, norpA, and its role in phototransduction. Cell 54(5): 723-33. 88311074

Chyb, S., Raghu, P. and Hardie, R. C. (1999). Polyunsaturated fatty acids activate the Drosophila light-sensitive channels TRP and TRPL. Nature 397(6716): 255-9. PubMed Citation: 9930700

Collins, B. H., Rosato, E. and Kyriacou, C. P. (2004). Seasonal behavior in Drosophila melanogaster requires the photoreceptors, the circadian clock, and phospholipase C. Proc. Natl. Acad. Sci. 101: 1945-1950. 14766972

Cook, B., BarYaacov, M., BenAmi, H. C., Goldstein, R. E., Paroush, Z., Selinger, Z. and Minke, B. (2000). Phospholipase C and termination of G-protein-mediated signalling in vivo. Nature Cell Biol. 2: 296-301. 10806481

Dasgupta, U., et al. (2009). Ceramide kinase regulates phospholipase C and phosphatidylinositol 4, 5, bisphosphate in phototransduction. Proc. Natl. Acad. Sci. 106(47): 20063-8. PubMed Citation: 19892737

Doh, S., et al. (1997). Promoter region of the Drosophila melanogaster norpA gene. Mol. Cells 7(6): 795-9. PubMed Citation: 9509423

Ferreira, P. A., Shortridge, R. D. and Pak, W. L. (1993). Distinctive subtypes of bovine phospholipase C that have preferential expression in the retina and high homology to the norpA gene product of Drosophila. Proc. Natl. Acad. Sci. 90(13): 6042-6. PubMed Citation: 8327481

Ferreira, P. A. and Pak, W. L. (1994). Bovine phospholipase C highly homologous to the NorpA protein of Drosophila is expressed specifically in cones. J. Biol. Chem. 269(5): 3129-31. PubMed Citation: 8106345

Glaser, F. T. and Stanewsky, R. (2005). Temperature synchronization of the Drosophila circadian clock. Curr. Biol. 15: 1352-1363. PubMed Citation: 16085487

Gu, G. G. and Singh, S. (1997). Modulation of the dihydropyridine-sensitive calcium channels in Drosophila by a phospholipase C-mediated pathway. J. Neurobiol. 33(3): 265-75. PubMed Citation: 9298764

Ha, E. M., et al. (2005a). A direct role for dual oxidase in Drosophila gut immunity. Science 310: 847-850. PubMed Citation: 16272120

Ha, E. M., et al (2005b). An antioxidant system required for host protection against gut infection in Drosophila. Dev. Cell 8: 125-132. PubMed Citation: 15621536

Ha, E. M., et al. (2009). Regulation of DUOX by the Galphaq-phospholipase Cbeta-Ca2+ pathway in Drosophila gut immunity. Dev. Cell 16(3): 386-97. PubMed Citation: 19289084

Hardie, R. C. and Raghu, P. (1998). Activation of heterologously expressed Drosophila TRPL channels: Ca2+ is not required and InsP3 is not sufficient. Cell Calcium 24(3): 153-63. PubMed Citation: 9883270

Hardie, R. C., et al. (2002). Molecular basis of amplification in Drosophila phototransduction: Roles for G Protein, Phospholipase C, and Diacylglycerol kinase. Neuron 36: 689-701. 12441057

Huber, A., Sander, P. and Paulsen, R. (1996a). Phosphorylation of the InaD gene product, a photoreceptor membrane protein required for recovery of visual excitation. J. Biol. Chem. 271(20): 11710-7

Huber, A., et al. (1996b). The transient receptor potential protein (Trp), a putative store-operated Ca2+ channel essential for phosphoinositide-mediated photoreception, forms a signaling complex with NorpA, InaC and InaD. EMBO J. 15(24): 7036-45

Huber, A., et al. (1998). The TRP Ca2+ channel assembled in a signaling complex by the PDZ domain protein INAD is phosphorylated through the interaction with protein kinase C (ePKC). FEBS Lett. 425(2): 317-22

Jiang, H., Wu, D. and Simon, M. I. (1994). Activation of phospholipase C beta 4 by heterotrimeric GTP-binding proteins. J. Biol. Chem. 269(10): 7593-6

Jiang, H., et al. (1996). Phospholipase C beta 4 is involved in modulating the visual response in mice. Proc. Natl. Acad. Sci. 93(25): 14598-601

Kile, B. T., et al. (2002). The SOCS box: a tale of destruction and degradation. Trends Biochem Sci. 27: 235-241. PubMed Citation: 12076535

Kim, D., et al. (1997). Phospholipase C isozymes selectively couple to specific neurotransmitter receptors. Nature 389(6648): 290-3

Kim, M. J., et al. (1993). Cloning of cDNA encoding rat phospholipase C-beta 4, a new member of the phospholipase C. Biochem. Biophys. Res. Commun. 194(2): 706-12

Kim, M. J., et al. (1998). A cytosolic, galphaq- and betagamma-insensitive splice variant of phospholipase C-beta4. J. Biol. Chem. 273(6): 3618-24

Kim, S., et al. (1995). Multiple subtypes of phospholipase C are encoded by the norpA gene of Drosophila melanogaster. J. Biol. Chem. 270(24): 14376-82

Kohn, E., Katz, B., Yasin, B., Peters, M., Rhodes, E., Zaguri, R., Weiss, S. and Minke, B. (2015) Functional cooperation between the IP3 receptor and Phospholipase C secures the high sensitivity to light of Drosophila photoreceptors in vivo. J Neurosci 35: 2530-2546. PubMed ID: 25673847

Koyanagi, M., et al. (1998). Phospholipase C cDNAs from sponge and hydra: antiquity of genes involved in the inositol phospholipid signaling pathway. FEBS Lett. 439(1-2): 66-70.

Lee, C. W., et al. (1993). Purification, molecular cloning, and sequencing of phospholipase C-beta 4. J. Biol. Chem. 268(28): 21318-27

Lee, C. W., et al. (1994). Regulation of phospholipase C-beta 4 by ribonucleotides and the alpha subunit of Gq. J. Biol. Chem. 269(41): 25335-8

Lee, S. J., Xu, H., Kang, L. W., Amzel, L. M. and Montell, C. (2003). Light adaptation through phosphoinositide-regulated translocation of Drosophila visual arrestin. Neuron 39(1):121-32. 12848937

Lee, Y. J., et al. (1994). The Drosophila dgq gene encodes a G alpha protein that mediates phototransduction. Neuron 13(5): 1143-57

Leung, H. T., Tseng-Crank, J., Kim, E., Mahapatra, C., Shino, S., Zhou, Y., An, L., Doerge, R. W. and Pak, W. L. (2008). DAG lipase activity is necessary for TRP channel regulation in Drosophila photoreceptors. Neuron 58(6): 884-96. PubMed Citation: 18579079

McKay, R. R., et al. (1994a). The rpa (receptor potential absent) visual mutant of the blowfly (Calliphora erythrocephala) is deficient in phospholipase C in the eye. J. Neurogenet. 9(3):177-87

McKay, R. R., Zhu, L. and Shortridge, R. D. (1994b). Membrane association of phospholipase C encoded by the norpA gene of Drosophila melanogaster. Neuroscience 61(1): 141-8

McKay, R. R., et al. (1995). Phospholipase C rescues visual defect in norpA mutant of Drosophila melanogaster. J. Biol. Chem. 270(22): 13271-6

Meyertholen, E. P., et al. (1987). Studies of the Drosophila norpA phototransduction mutant. II. Photoreceptor degeneration and rhodopsin maintenance. J. Comp. Physiol. [A]161(6): 793-8

Mitchell, J. and Mayeenuddin, L. H. (1998). Purification, G protein activation, and partial amino acid sequence of a novel phospholipase C from squid photoreceptors. Biochemistry 37(25): 9064-72

Niemeyer, B. A., et al. (1996). The Drosophila light-activated conductance is composed of the two channels TRP and TRPL. Cell 85(5): 651-9

Pearn, M. T., et al. (1996). Molecular, biochemical, and electrophysiological characterization of Drosophila norpA mutants. J. Biol. Chem. 271(9): 4937-45

Peretz, A., et al. (1994). The light response of Drosophila photoreceptors is accompanied by an increase in cellular calcium: effects of specific mutations. Neuron 12(6): 1257-67

Ranganathan, R., et al. (1994). Cytosolic calcium transients: spatial localization and role in Drosophila photoreceptor cell function. Neuron 13(4): 837-48

Riesgo-Escovar, J., Raha, D. and Carlson, J. R. (1995). Requirement for a phospholipase C in odor response: overlap between olfaction and vision in Drosophila. Proc. Natl. Acad. Sci. 92(7): 2864-8

Roustan, P., et al. (1995). The rat phospholipase C beta 4 gene is expressed at high abundance in cerebellar Purkinje cells. Neuroreport 6(14): 1837-41

Running Deer, J. L., Hurley, J. B. and Yarfitz, S. L. (1995). G protein control of Drosophila photoreceptor phospholipase C. J. Biol. Chem. 270(21): 12623-8

Ryu, J. H., et al. (2008). Innate immune homeostasis by the homeobox gene caudal and commensal-gut mutualism in Drosophila. Science 319: 777-782. PubMed Citation: 18218863

Schneuwly, S., et al. (1991). Properties of photoreceptor-specific phospholipase C encoded by the norpA gene of Drosophila melanogaster. J. Biol. Chem. 266(36): 24314-9

Scott, K., et al. (1995). Gq alpha protein function in vivo: genetic dissection of its role in photoreceptor cell physiology. Neuron 15(4): 919-27

Shen, W. L., et al. (2011). Function of rhodopsin in temperature discrimination in Drosophila. Science 331(6022): 1333-6. PubMed Citation: 21393546

Shieh, B. H., Zhu, M. Y., Lee, J. K., Kelly, I. M. and Bahiraei, F. (1997). Association of INAD with NORPA is essential for controlled activation and deactivation of Drosophila phototransduction in vivo. Proc. Natl. Acad. Sci. 94(23): 12682-12687

Shortridge, R. D., et al. (1991). A Drosophila phospholipase C gene that is expressed in the central nervous system. J. Biol. Chem. 266(19): 12474-80

Stark, W. S., Sapp, R. and Carlson, S. D. (1989). Photoreceptor maintenance and degeneration in the norpA (no receptor potential-A) mutant of Drosophila melanogaster. J. Neurogenet. 5(1): 49-59

Toyoshima, S., et al. (1990). Purification and partial amino acid sequences of phosphoinositide-specific phospholipase C of Drosophila eye. J. Biol. Chem. 265(25): 14842-8

Tsunoda, S., et al. (1997). A multivalent PDZ-domain protein assembles signalling complexes in a G-protein-coupled cascade. Nature 388(6639): 243-9

van Huizen, R., et al. (1998). Two distantly positioned PDZ domains mediate multivalent INAD-phospholipase C interactions essential for G protein-coupled signaling. EMBO J. 17(8): 2285-97

Wang, T., Wang, X., Xie, Q. and Montell, C. (2008). The SOCS box protein STOPS is required for phototransduction through its effects on phospholipase C. Neuron 57(1): 56-68. PubMed Citation: 18184564

Wilson, M. J. and Ostroy, S. E. (1987). Studies of the Drosophila norpA phototransduction mutant. I. Electrophysiological changes and the offsetting effect of light. J. Comp. Physiol. [A] 161(6): 785-91. 88118417

Yoshioka, T., Inoue, H., Hotta, Y. (1985). Absence of phosphatidylinositol phosphodiesterase in the head of a Drosophila visual mutant, norpA (no receptor potential A). J. Biochem. 97: 1251-1254. 85289108

Zhu, L., McKay, R. R. and Shortridge, R. D. (1993). Tissue-specific expression of phospholipase C encoded by the norpA gene of Drosophila melanogaster. J. Biol. Chem. 268(21): 15994-6001


Biological Overview

date revised: 20 August 2011

Home page: The Interactive Fly © 2017 Thomas Brody, Ph.D.