In order to establish that a Ccap-GAL4 transgene accurately reproduces the expression of the Ccap gene, it was first used to drive expression of the reporter lacZ, and the spatial expression of the reporter was compared to that of Ccap. In Drosophila, the Ccap peptide is consistently expressed in 2 pairs of neurons in the brain, 5 pairs in the subesophageal ganglion, 1-2 pairs in at least 8 ganglia of the ventral nervous system (ventral nervous system), as well as in 2 pairs of strongly immunoreactive descending axons, one lateral and one medial (see Ewer and Truman, 1996). No evidence of changes in the number of neurons that express Ccap-IR during postembryonic development was found except following adult eclosion, when there is a precipitous decrease in the number of Ccap neurons due to their elimination by programmed cell death (Draizen, 1999). Thus, unlike the situation in Manduca (Davis, 1993; Loi, 2001), no CCAP immunoreactive neurons appear to be added to the pattern that is established by the 1st instar larval stage (Park, 2003).
GAL4 fusions bearing the -516 to +39 bp fragment of 5' Ccap DNA faithfully reproduce the temporal and spatial pattern of Ccap expression. Thus, in all cases examined, neurons that are Ccap immunoreactive are also ß-gal immunoreactive, and vice versa. The stages examined included 1st instar (0- to 2-hour, 6- to 8-hour and 21- to 24-hour-old 1st instars), mid- and late-2nd instar, pharate and wandering 3rd instar larvae, pharate pupae, pharate adults, and 6-day-old adults (late 2nd instar). All three independent transformant lines bearing this construct showed indistinguishable patterns of expression (Park, 2003).
The effect of crustacean cardioactive peptide on Drosophila heart rate was measured in the animal and in a tissue preparation. Crustacean cardioactive peptide increases in vivo basal heart rate 1%, 6%, and 19% and increases in vitro basal heart rate 52%, 25%, and 35% in larvae, pupae, and adults, respectively. In the tissue preparation, the acceleratory period is followed by decreased in vitro heart rates of 42%, 16%, and 13% in larvae, pupae, and adults, respectively. The effects observed in the animal and tissue and in larvae, pupae, and adults suggest that Drosophila crustacean cardioactive peptide cardiac signaling is modulated and developmentally regulated (Nichols, 1999).
At the end of each molt, insects shed their old cuticle by performing the ecdysis sequence, an innate behavior consisting of three steps: pre-ecdysis, ecdysis, and postecdysis. Blood-borne ecdysis-triggering hormone (ETH) activates the behavioral sequence through direct actions on the central nervous system. To elucidate neural substrates underlying the ecdysis sequence, neurons expressing ETH receptors (ETHRs) have been identified in Drosophila. Distinct ensembles of ETHR neurons express numerous neuropeptides including kinin, FMRFamides, eclosion hormone (EH), crustacean cardioactive peptide (CCAP), myoinhibitory peptides (MIP), and bursicon. Real-time imaging of intracellular calcium dynamics revealed sequential activation of these ensembles after ETH action. Specifically, FMRFamide neurons are activated during pre-ecdysis; EH, CCAP, and CCAP/MIP neurons are active prior to and during ecdysis; and activity of CCAP/MIP/bursicon neurons coincides with postecdysis. Targeted ablation of specific ETHR ensembles produces behavioral deficits consistent with their proposed roles in the behavioral sequence. These findings offer novel insights into how a command chemical orchestrates an innate behavior by stepwise recruitment of central peptidergic ensembles (Kim, 2006a).
Analysis of the pupal ecdysis behavioral sequence: In Drosophila, pupal ecdysis is preceded by pupariation, whereby the prepupa contracts its body into a barrel shape to form the puparium composed of the old larval cuticle. The underlying new pupal cuticle then separates from the puparium during pupal ecdysis ~12 hr later. The stereotypic nature of pupal ecdysis and reliable developmental markers make it a favorable model for the behavioral analysis and neural imaging (Kim, 2006a).
Pupal ecdysis consists of three centrally patterned behavioral subunits performed sequentially: pre-ecdysis (~10 min), ecdysis (~5 min), and postecdysis (~60-70 min). The behavioral sequence was examined through the semitransparent puparium ('puparium-intact'), but it was found that the puparium obscures and places constraints on some movements. This made it particularly difficult to discriminate differences in abdominal swinging movements during ecdysis and postecdysis. Therefore, a 'puparium-free' preparation was used by surgically removing the puparium immediately after pre-ecdysis onset. The improved visibility and room for movement in this preparation allowed for a more complete analysis of natural and ETH-induced behavior. The following description of the natural pupal ecdysis sequence resulted from comparison of behaviors observed in both puparium-intact and puparium-free prepupae (Kim, 2006a).
Pre-ecdysis: About 5 min after in vivo ETH release, preecdysis commences with the abrupt appearance of an air bubble at the posterior end of the prepupa (time zero). Pre-ecdysis involves anteriorly directed rolling contractions along the lateral edges of the abdomen, alternating on the left and right sides of the animal. These contractions move the air bubble anteriorly to separate pupal cuticle from the puparium. This behavior is completed within ~10 min and is followed by ecdysis behavior. Preecdysis behavior is the same in puparium-intact and puparium-free animals (Kim, 2006a).
Ecdysis: In higher Diptera including Drosophila, the incipient adult head develops within the prepupal thorax. During pupal ecdysis, head eversion results from lateral swinging movements of the abdomen occurring along with anteriorly directed peristaltic contractions. In puparium-intact preparations, head eversion occurs ~1 min after the onset of ecdysis swinging and is completed within ~5s. After completion of head eversion, ecdysis contractions continue for ~15 min, facilitating expansion of wing pads and legs to their final size. The frequency of ecdysis swinging (~5 swings/min) decreases markedly after head eversion (~2 swings/min). In puparium-free animals, head eversion occurs sooner, and the duration of ecdysis behavior lasts only ~5 min. Later in ecdysis, anteriorly directed swinging contractions are often interrupted by posteriorly directed ones, indicating a transition to postecdysis (Kim, 2006a).
Postecdysis: Postecdysis behavior consists of two behavioral subroutines: postecdysis swinging and stretch-compression movements of the abdomen. Postecdysis swinging occurs along with posteriorly directed peristaltic contractions and alternates with longitudinal movements of the abdomen, referred to as 'stretch-compression.' The frequency and intensity of postecdysis contractions wane gradually until they are detected mainly in the anterior part of the abdomen; they cease w100 min after pre-ecdysis onset. Postecdysis behavior concludes with compression of the pupa at the posterior end of the puparium (Kim, 2006a).
ETH release coincides with initiation of the ecdysis sequence: To confirm the role of ETH in initiation of the pupal ecdysis sequence, its release from endocrine Inka cells was monitored in vivo by using time-lapse EGFP fluorescence imaging in pharate pupae (prepupae) carrying the chimeric transgene 2eth3-egfp. In this transgenic fly, EGFP is expressed as part of a fusion protein with the ETH propeptide precursor, and loss of EGFP fluorescence indicates ETH release. Because pharate pupae generally are immobile and Inka cells are located immediately below the semitransparent puparium, in situ imaging of Inka cell in intact pharate pupae is feasible. Two to three Inka cells were monitored simultaneously in each experiment (Kim, 2006a).
Depletion of ETH-EGFP occurs in about 50% of monitored Inka cells shortly before pre-ecdysis onset (time zero). The time course of secretory activity for each Inka cell was variable. The mean value for the timing of ETH release was 4.5 min prior to pre-ecdysis onset, and the duration of ETH secretion was 4.4. In contrast, 40% of Inka cells showed no sign of secretory activity by pre-ecdysis onset. After initiation of pre-ecdysis contractions, it was usually impossible to continue monitoring loss of EGFP fluorescence as a result of movement artifacts. All Inka cells are depleted of ETH-EGFP by the end of ecdysis sequence (Kim, 2006a).
Injection of ETH induces the ecdysis sequence: Because ETH release coincides with onset of pupal preecdysis, it was of interest to determine whether ETH injection would trigger the pupal ecdysis sequence. The Drosophila gene eth encodes a precursor producing one copy each of two peptides, ETH1 and ETH2, which share similar structure and biological activity. In vivo experiments were carried out primarily in puparium-free preparations (Kim, 2006a).
Injection of ETH1 alone into pharate pupae (~1-2 hr prior to natural ecdysis) induced within 1-3 min strong pre-ecdysis contractions followed by ecdysis and postecdysis contractions sequentially. ETH-induced pre-ecdysis showed a strong dose dependence, with higher doses inducing shorter pre-ecdysis duration and higher frequency of contractions. Similar but somewhat less pronounced dose-dependent effects were observed during ecdysis behavior, whereas the frequency of postecdysis contractions showed little or no dose dependence during the first 10 min of behavior (Kim, 2006a).
Injection of ETH2 was less efficacious for induction of the behavioral sequence compared to ETH1. ETH2 generated prolonged pre-ecdysis behavior lasting to 50 min or more, but no ecdysis behavior. In contrast, injection of the same dose of ETH1 (0.4 pmol) produced the complete behavioral sequence consisting of pre-ecdysis, ecdysis, and postecdysis. Higher doses of ETH2 (20 pmol) generated a behavioral sequence comparable to that induced by 4 pmol ETH1 in terms of pre-ecdysis duration and frequency of contractions. Behaviors after injecting a cocktail of ETH1 and ETH2 (0.4 pmol of each peptide) were also examined. Because the two peptides are processed from the same precursor, it is likely that these peptides are coreleased under natural conditions. The duration of the behavioral sequence induced by injection of the cocktail was similar to the naturally occurring sequence or one induced by 0.4 pmol ETH1 alone. It is estimated that a 0.4 pmol ETH injection into a prepupa w10 hr after puparium formation results in a concentration of ~300 nM in vivo (Kim, 2006a).
ETH receptors are expressed in diverse ensembles of peptidergic neurons: ETH acts directly on the CNS to initiate the ecdysis behavioral sequence in moths and flies via unknown signaling pathways within the CNS. A starting point for elucidation of these downstream signaling pathways is identification of primary neuronal targets of ETH. The ETH receptor gene (CG5911), first identified in Drosophila, encodes two G protein-coupled receptors, ETHR-A and ETHR-B, via alternative splicing. In situ hybridization was used for identification of central neurons expressing ETHR-A and ETHR-B by using DNA probes specific for each receptor subtype. ETHR-A and ETHR-B transcripts were located in mutually exclusive populations of neurons distributed throughout the CNS, suggesting that two subtypes of ETH receptors likely mediate different functions. Further analysis revealed that most ETHR-A neurons are peptidergic. Neurons expressing ETHR-B have not been identified thus far (Kim, 2006a).
Multiple ensembles of ETHR-A neurons are classified according to specific neuropeptides they express. Peptides expressed in these ensembles were identified by using GAL4 transgenes under control of neuropeptide promoters to drive UAS-GFP or UAS-GCaMP expression (GAL4::GFP or GAL4::GCaMP). Expression of neuropeptides in these cells was confirmed by combining immunohistochemical staining and in situ hybridization. The first ETHR-A ensemble comprises six pairs of lateral abdominal neurons producing kinin, also known as drosokinin. These cells project axons posteriorly along the lateral edge of the neuropile and then turn anteriorly along the midline of ventral nerve cord, where they arborize and form possible central release sites. Axons of these cells also exit the CNS through nerve roots, suggesting peripheral kinin release. The second ETHR-A ensemble contains three pairs of ventrolateral FMRFamide neurosecretory cells (Tv1-3 or T1-3) in the thoracic neuromeres TN1-3. These cells project axons into the dorsomedial neurohemal organs (NHOs) specialized for peptide release into the hemolymph (Kim, 2006a).
The third class of ETHR-A neurons comprises the eclosion hormone (EH)-producing VM neurons in the brain, which project one axonal branch anteriorly into the neurohemal ring gland and a second posteriorly along the dorsal midline of the entire ventral nerve cord. The fourth ETHR-A ensemble is composed of paired dorsolateral neurons producing CCAP, MIPs, and bursicon in subesophageal, thoracic, and abdominal neuromeres (SN1-3, TN1-3, AN1-7, respectively). These cells are likely homologs of moth neurons 27/704, on the basis of their anatomy, peptide coexpression profile, and functional roles during pupal ecdysis. These neurons are referred to as Drosophila neurons 27/704 and them were subdivided on the basis of peptide coexpression. In AN1-4, CCAP is colocalized with MIPs and the heterodimeric peptide hormone bursicon (composed of burs and pburs subunits). In TN2-3 and AN5- 9, CCAP is colocalized with burs, but pburs is not expressed in these neurons. Finally, CCAP is colocalized with MIPs in large paired neurons of AN8,9, but ETHR-A expression has not been confirmed in these cells. The presence of MIP mRNA in abdominal neurons 27/704 was further confirmed by in situ hybridization (Kim, 2006a).
Ca2+ imaging of primary ETH targets in transgenic flies: Having shown that ETH receptors occur in diverse ensembles of peptidergic neurons, it was asked whether these cells are activated by ETH and whether this activity coincides with specific behavioral steps of the ecdysis sequence. Calcium dynamics in each group of ETHR-A neurons was monitored by driving expression of the GFP-based Ca2+ sensor, GCaMP [23, 24], in genetically defined sets of neurons with the binary GAL4/UAS system. Ca2+ elevation induces a conformational change of GCaMP, increasing its GFP fluorescence. Using optical imaging of GFP fluorescence, [Ca2+]i dynamics of ETHR neurons were monitored, and these events were associated with each behavioral phase induced by ETH (Kim, 2006a).
An abundance of evidence indicates that the ecdysis behavioral sequence in insects is centrally patterned. In particular, the onset and duration of each behavior in the sequence (pre-ecdysis I, pre-ecdysis II, ecdysis) is the same whether observed in vivo or as fictive behavior recorded from the isolated CNS in vitro. On the basis of this evidence, [Ca2+]i dynamics of ETHR-A neuron ensembles of the isolated CNS were associated with behaviors observed in puparium-free preparations (Kim, 2006a).
FMRFamide neurons and their neurohemal endings become active early in pre-ecdysis: [Ca2+]i levels were monitored in ETHR-A/FMRFamide Tv neurons by preparing transgenic flies doubly homozygous for FMRFa-GAL4 and UAS-GCaMP. Prior to ETH1 exposure (4-6 hr prior to ecdysis), Tv cell bodies and neurohemal endings in the dorsomedial NHO exhibit low levels of basal GCaMP fluorescence (Kim, 2006a).
Exposure of the CNS to ETH1 (600 nM) elicits robust increases in calcium-associated fluorescence in cell bodies and axon terminals of all Tv neurons. At this concentration of ETH1, calcium dynamics typically are characterized by transient, spike-shaped fluctuations superimposed upon a slow upward shift of the baseline, beginning ~8 min after exposure to the peptide. This response lasts ~10-15 min, after which weaker spike-like fluctuations continue without baseline changes until the end of recordings (~40 min). It is estimated that a concentration of 600 nM ETH1 results from a dose of w0.4 pmol of the peptide in vivo. Thus the major calcium response of Tv neurons coincides with the early phase of pre-ecdysis, and weaker activity persists through ecdysis and postecdysis. In contrast, ETH2 alone (600 nM) generates Ca2+ responses after a longer delay comparable to one following exposure to 60 nM ETH1. The longer delay of Ca2+ responses after ETH2 fits with the observations of in vivo behavior, where ETH2 is a less potent agonist than ETH1. The cocktail of ETH1 and ETH2 (600 nM each) evokes Ca2+ dynamics after a delay similar to that induced by ETH1 alone. Overall, [Ca2+]i dynamics observed in Tv neurons are synchronized. In many preparations, Tv neurons from the same neuromere appear to be strongly coupled, given that they produce precisely synchronized Ca2+ dynamics. Transient Ca2+ signals are obvious in the terminal processes of Tv neurons in NHO, the release sites of FMRFamides (Kim, 2006a).
Lower concentrations of ETH1 elicit calcium dynamics after a somewhat longer delay. Interestingly, calcium dynamics are obvious first in neurohemal endings of the NHO, followed by fluctuations in cell bodies. This was particularly evident at 60 nM ETH1, where a robust calcium response in the NHO was accompanied by only a weak response in the Tv2 cell body. No calcium responses are observed in Tvs exposed to 6 nM ETH1 (Kim, 2006a).
EH neurons reach peak activity at ecdysis: VM neurons producing eclosion hormone (EH) have been implicated as primary ETH targets during fly and moth ecdysis. Expression of ETHR-A was demonstrated in VM neurons, confirming that they are primary ETH targets. To determine whether ETH elicits activity in EH neurons, transgenic flies were prepared doubly homozygous for EHup-GAL4 and UASGCaMP, that show GCaMP fluorescence only in these cells (Kim, 2006a).
EH neurons are highly sensitive to ETH1, exhibiting robust [Ca2+]i dynamics upon exposure to concentrations as low as 6 nM. No detectable fluorescence responses are observed after exposure to 0.6 nM ETH1 over a period of 50-60 min. The latency to Ca2+ responses is inversely proportional to the concentration of ETH1; higher ETH1 concentrations evoke faster responses. The cocktail of ETH1 and ETH2 (600 nM each) elicited Ca2+ responses after a ~10-15 min delay (Kim, 2006a).
Close examination of these ETH-evoked fluorescence responses reveals two components distinguished by slow and fast kinetics. The slow component is characterized by a gradual increase in baseline levels of Ca2+ followed by a decrease over 20-30 min, whereas the fast component is composed of transient, spike-like activity. Fast components have durations ranging from 5-20 s. Peak DF/F responses are quite variable, even among a group of neurons exposed to the same ETH1 concentration. No significant concentration dependence could be detected in peak response (Kim, 2006a).
Distinct subsets of neurons 27/704 are active during different phases of the ecdysis sequence: ETH-evoked Ca2+ signals of neurons 27/704 were examined in transgenic flies carrying CCAP-GAL4 and UAS-GCaMP. Use of the CCAP promoter to drive GCaMP expression resulted in a reporter pattern identical to that described previously. Upon exposure to 600 nM ETH1, distinct subsets of neurons 27/704 exhibited reproducible, stereotypic Ca2+ responses in terms of peak intensity, latency, and termination of Ca2+ dynamics. According to the magnitude of peak fluorescence intensity (peak DF/F), neurons 27/704 fall into three major groups: strong responders, weak responders, and nonresponders. The strong-responder group includes neurons 27/704 in AN1-4 (CCAP/MIPs/bursicon), AN8,9 (CCAP/ MIPs), and TN3 (CCAP). Weak responders are neurons 27/704 in SN2-3, TN1-2, and AN7 producing CCAP only. Neurons in the brain, SN1, and AN5,6 showed no reproducible Ca2+ dynamics in response to 600 nM ETH1 (Kim, 2006a).
In response to ETH1, neurons 27/704 in TN3 and AN8,9 become active within 10-15 min, whereas neurons 27/704 in AN1-4 are activated after a 15-25 min delay. Neurons in TN3 and AN8,9 are therefore activated just prior to ecdysis onset, indicating their possible roles in initiation and maintenance of ecdysis behavior. In addition, Ca2+ dynamics observed in AN8,9 neurons terminated early in postecdysis, supporting this interpretation. In contrast, Ca2+ dynamics of neurons in AN1-4 begin during ecdysis and increase in intensity during the entire postecdysis period, suggesting their roles in these events. The cocktail of ETH1 and ETH2 (600 nM each) evoked Ca2+ dynamics similar to those induced by ETH1 alone. Two groups of neurons 27/704 in abdominal neuromeres (AN1-4 versus AN8,9) exhibit differences in sensitivity to ETH and in their patterns of [Ca2+]i dynamics. It was found that 6-60 nM ETH1 activates neurons in AN1-4 (n = 4), whereas higher concentrations of ETH1 (R600 nM) are required to activate neurons in AN8,9. In addition, neurons in AN8,9 generate transient (1-2 min) Ca2+ spikes over a 15-20 min period after ETH1 activation, whereas neurons in AN1-4 generally produce slower, more persistent Ca2+ dynamics. These differences among subgroups of neurons 27/704 suggest their different functional roles during the ecdysis sequence (Kim, 2006a).
Targeted ablations of apecific ETHR neurons have behavioral consequences: To evaluate behavioral roles of specific ETHR neurons, phenotypes of the pupal ecdysis sequence were investigated in transgenic flies bearing targeted ablations of ETHR neurons, including Tv FMRFamide neurons, EH neurons, and CCAP neurons (27/704 homologs). In control flies carrying UAS-reaper and UAS-GCaMP, but lacking the GAL4 driver, pupal ecdysis was executed as in wild-type flies: pre-ecdysis (0-10 min), ecdysis (10-23 min), and postecdysis (23-100 min) (Figure 7). Given that puparium-intact animals were used, the duration of ecdysis behavior may have been overestimated. Transgenic flies bearing targeted ablations of Tv FMRFamide neurons (FMRF-KO) were generated by crossing females doubly homozygous for FMRFa-GAL4, UAS-GCaMP with homozygous UAS-reaper males. Pupal ecdysis of FMRFa-KO flies is very similar to that of control flies. Because FMRFa-GAL4 drives expression of GAL4 only in three pairs of thoracic Tv neurons and one pair of unidentified neurons in SN, FMRFa-KO flies lost only Tv neurons and not other FMRFamide neurons in the CNS. FMRFa-KO flies complete pupal ecdysis without any detectable abnormality, except that pre-ecdysis contractions appear weaker than in control flies. Pupal ecdysis of VM neuron knockout flies (EH-KO) was then examined. Behavioral analysis showed that, although they complete pupal ecdysis without any severe defects or lethality, ecdysis onset is delayed w4 min. As a result of this delay, EH-KO flies show longer pre-ecdysis than control flies. Additional parameters governing pre-ecdysis, ecdysis, and postecdysis are indistinguishable between EH-KO and control flies (Kim, 2006a).
Finally, CCAP-KO flies were generated in order to examine the functional roles of neurons 27/704 (CCAP neurons) in pupal ecdysis. As expected, CCAP-KO flies failed to initiate ecdysis contractions and could not complete head eversion. Instead, they show prolonged pre-ecdysis contractions for ~25 min, followed by weak random contractions of the abdomen (different from ecdysis and postecdysis contractions of control flies) for the next 50 min (Kim, 2006a).
Conclusions: This study has described orchestration of an innate behavior, the Drosophila pupal ecdysis sequence, by the endocrine peptide ETH. ETH release coincides with onset of behavior, and injection of ETH triggers the complete behavioral sequence, consistent with its role in ecdysis activation previously established in the moths Manduca sexta and Bombyx mori and in Drosophila larvae and adults. Absence of ETH causes lethal ecdysis deficiency, a phenotype that is rescued by ETH injection. ETH therefore functions as a 'command chemical' to orchestrate an innate behavior. Primary CNS targets of ETH was identified by using ETHR-specific in situ hybridization. ETHR-A occurs in multiple classes of peptidergic neurons producing EH, CCAP/MIPs/bursicon, FMRFamides, or kinin (Kim, 2006a).
Expression of ETHR-A was shown in VM neurons, which release EH. In response to ETH, VM neurons become active prior to ecdysis behavior and reach peak levels of activity during ecdysis. These results provide further support for a previously described positive-feedback signaling pathway between VM neurons and Inka cells. This feedback is thought to ensure depletion of ETH from Inka cells. These findings are striking because independent evidence indicates that homologous VM neurons in the moth Manduca are direct targets of ETH and that their secretory products regulate ecdysis behaviors downstream of ETH. For example, isolated EH neurons of Manduca respond to direct action of ETH with increased excitability and spike broadening. In response to ETH action, these neurons release EH, causing cGMP elevation and increased excitability in CCAP-containing neurons 27/704 of the thoracic and abdominal ganglia. CCAP and MIPs, cotransmitters produced by neurons 704, are implicated in eliciting ecdysis behavior (Kim, 2006a).
A homologous role for EH in activation of Drosophila 27/704 neurons has not been clearly demonstrated. For example, no cGMP elevation is observed in these neurons during the natural ecdysis sequence. This lack of cGMP elevation suggests that CCAP neurons are not directly targeted by EH in Drosophila. Nevertheless, EH-knockout flies exhibit a delay in ecdysis initiation, suggesting that EH may modulate excitability in 27/704 cells indirectly through release of additional factors within the CNS. It is therefore proposed that activation of EH neurons by ETH serves two purposes: (1) release of EH into the hemocoel functions as part of a positive-feedback pathway to ensure ETH depletion from Inka cells; (2) release of EH within the CNS synergizes direct ETH actions on different subsets of neurons 27/704 producing CCAP, MIPs, and bursicon, perhaps indirectly through release of downstream signals within the CNS (Kim, 2006a).
Neurons 27/704 expressing ETHR-A respond to ETH with unique patterns of Ca2+ dynamics. These neurons are subdivided by pattern of transmitter expression: CCAP/MIPs/bursicon in AN1-4; CCAP/MIPs in AN8,9; and CCAP in SN1-3, TN1-3, and AN5-7. Temporal patterns of Ca2+ dynamics were determined in each neuronal subset relevant to the behaviors observed. On the basis of these temporal patterns, it is proposed that direct action of ETH on neurons 27/704 in TN3 and in AN8,9 induces initiation and execution of ecdysis contractions and head eversion. In support of this, it is shown that ablation of CCAP neurons abolishes ecdysis contractions and head eversion. Parallel study in Manduca showed that neurons 704 expressing ETHR-A and their peptide cotransmitters, CCAP and MIPs, are implicated in control of the ecdysis motor pattern, supporting the homologous function of 27/704 neurons in Drosophila. Neurons 27/704 in AN1-4 produce CCAP, MIPs, and bursicon, and therefore a cocktail of these peptides is likely released within the CNS and into the hemolymph during postecdysis. It is suggested that centrally released peptides control postecdysis movements, whereas blood-borne CCAP/MIPs regulate heart beat and blood pressure for cuticle expansion and bursicon controls sclerotization of expanded new cuticle. Bursicon was recently identified as a heterodimeric peptide hormone regulating cuticle plasticization, sclerotization, and melanization (Kim, 2006a).
The Drosophila FMRFamide gene (FMRFa) encodes multiple FMRFamide-related neuropeptides, which are expressed in many different cell types, including neuroendocrine cells, interneurons, and perhaps motoneurons. Among these diverse FMRFamide-producing neurons, ETHR-A expression is confined to three pairs of thoracic neurosecretory neurons, Tv1-3. Results of the present study show that the Tv neurons are activated early in pre-ecdysis and that they remain active during ecdysis and postecdysis. However, FMRFa-KO flies show no differences in timing of the ecdysis behavioral sequence. Because FMRFamides enhance twitch tension of larval body-wall muscles through synaptic modulation at the neuromuscular junction, blood-borne FMRFamides released from Tv neurons likely facilitates pre-ecdysis, ecdysis, and postecdysis contractions. Thus the role of Tv neurons as primary ETH targets may be enhancement of muscle contraction during the behaviors. Further work to substantiate this is in progress (Kim, 2006a).
Expression of ETHR-A occurs in in kinin neurons of abdominal neuromeres of Drosophila. Drosophila kinin is known to be involved in water balance, but its central functions have not been described or considered. Expression of ETHR-A in kinin neurons appears to be a conserved mechanism in fly and moth; the Manduca ETHR-A is expressed in abdominal neurosecretory cells (L3,4), which produce kinins and diuretic hormones (DHs). It was further found that the isolated Manduca CNS generates the fictive pre-ecdysis motor pattern upon exposure to a cocktail of kinin and DHs. These findings suggest that ETH activates L3,4 neurons in Manduca to release kinins and DHs centrally, which initiate and execute pre-ecdysis. On the basis of the conservation between Drosophila and Manduca in spatial expression pattern of ETHR, it is proposed that ETH initiates pre-ecdysis behavior indirectly via central release of kinin in Drosophila (Kim, 2006a).
In Drosophila, pupal ecdysis is accomplished by sequential recruitment of three major behavioral units: pre-ecdysis (0-10 min), ecdysis (10-15 min), and postecdysis (15-100 min). Each behavioral unit is programmed in the CNS and sequentially activated by direct actions of ETH, which is synthesized and released from peripheral endocrine Inka cells. Around 4-5 min before pre-ecdysis onset, a sizeable portion (~50%) of Inka cells initiates secretion of ETH into the hemolymph, whereas the remaining portion completes secretion after onset of pre-ecdysis. Appearance of ETH in the hemolymph activates ETHR-A in neurons expressing neuropeptides including kinin, FMRFamides (Tv1-3), EH, or CCAP, MIPs, and bursicon, but they are not released until descending inhibition is removed at key times during the ecdysis sequence. Upon activation of ETHR, the central release of kinin initiates pre-ecdysis contractions, whereas Tv neurons secrete FMRFamides to enhance neuromuscular transmission. ETH activates neurons producing EH, CCAP, CCAP/MIPs, and CCAP/MIPs/bursicon at different times. EH cells in the brain and neurons producing CCAP in TN3 and CCAP/MIPs in AN8,9 become active ~10-13 min after pre-ecdysis initiation. EH participates in timing the activation of ecdysis neurons, whereas CCAP and MIPs from TN3 and AN8,9 control initiation and execution of the ecdysis motor program. At the end of ecdysis (25 min after pre-ecdysis onset), neurons in AN1-4 secrete a cocktail of CCAP, MIPs, and bursicon, which likely regulate postecdysis contractions and processes associated with cuticle expansion, hardening, and tanning (Kim, 2006a).
This study has mapped central ETH receptor neurons, and discovered that they comprise multiple peptidergic ensembles, which are recruited sequentially to generate each phase of the ecdysis sequence. Ensemble-specific knockout analysis supports this interpretation. Each step of the ecdysis sequence (pre-ecdysis, ecdysis, postecdysis) is driven by a central pattern generator (CPG) within the CNS in the absence of sensory input. It is known that amines and peptides can modulate and reconfigure neuronal circuits comprising CPGs so as to elicit a variety of motor patterns. It seems likely that the multiple peptidergic ensembles described in this study as targets for ETH may be involved in configuring and activating CPGs underlying each step of the ecdysis sequence (Kim, 2006a).
Processes in the brain that govern behaviors over longer time frames such as sleep, mood, sexual activities, and even learning and memory could be associated with coordinated release of neuromodulators such as peptides. Further work on activation of central peptidergic ensembles in the CNS may shed light on mechanisms underlying release of a variety of behaviors (Kim, 2006a).
G-protein coupled receptors (GPCRs) are ancient, ubiquitous sensors vital to environmental and physiological signaling throughout organismal life. With the publication of the Drosophila genome, numerous 'orphan' GPCRs have become available for functional analysis. This study analyzes two groups of GPCRs predicted as receptors for peptides with a C-terminal amino acid sequence motif consisting of PRXamide (PRXa). Assuming ligand-receptor coevolution, two alternative hypotheses were constructed and tested. The insect PRXa peptides are evolutionarily related to the vertebrate peptide neuromedin U (NMU), or are related to arginine vasopressin (AVP), both of which have PRXa motifs. Seven Drosophila GPCRs related to receptors for NMU and AVP were cloned and expressed in Xenopus oocytes for functional analysis. Four Drosophila GPCRs in the NMU group (CG11475, CG8795, CG9918, CG8784) are activated by insect PRXa pyrokinins (FXPRXamide), Cap2b-like peptides (FPRXamide), or ecdysis triggering hormones (PRXamide). Three Drosophila GPCRs in the vasopressin receptor group respond to crustacean cardioactive peptide (CCAP), corazonin, or adipokinetic hormone (AKH), none of which are PRXa peptides. These findings support a theory of coevolution for NMU and Drosophila PRXa peptides and their respective receptors (Park, 2002b).
Examination of the three Drosophila GPCRs homologous to the AVP receptor yielded serendipitous findings. CG6111, orthologous to the vasopressin receptor, is activated by CCAP and AKH. CG10698 and CG11325 are activated by corazonin and AKH, respectively. The EC50 values for receptors in the AVP group are consistently lower than those observed in the NMU PRXa group (Park, 2002b).
It is surprising that CG6111, an orthologous gene of AVP receptor, is activated by CCAP and AKH, but not by AVP. The presence of an insect vasopressin-like peptide was reported in locust, but searches of the Drosophila genome sequence to locate a candidate AVP-like peptide sequence have been unsuccessful. CCAP and AVP both are C-terminally amidated, disulfide bridged peptides, but share no significant sequence similarity. The current data set favors assignment of CG6111 as an authentic CCAP receptor because of ligand cross-reactivity within this group of GPCRs. It seems reasonable to have residual functional cross-activity within recent evolutionarily diverged GPCRs. Further work is needed to verify whether CG6111 is an authentic CCAP receptor or is a receptor for unidentified Drosophila AVP-like peptide cross-reacting to the CCAP (Park, 2002b).
CG10698 is activated by corazonin with an EC50 of 1 nM. Similarly, CG11325, previously cloned by its homology to GNRHR, is activated by AKH with an EC50 of 0.3 nM. These evolutionarily related GPCRs, activated by structurally similar signaling peptides, reveals a clear case of receptor-ligand coevolution (Park, 2002b).
CCAP, corazonin, and AKH have overlapping biological functions, and thus it is not unexpected that their receptors would fall into an evolutionarily related group. CCAP was initially identified by its cardioacceleratory action on the heart of the shore crab and in the tobacco hawkmoth, Manduca. The primary structure of this peptide appears to be strictly conserved across the arthropods. Additional functions of CCAP include myotropic actions, induction of AKH release in corpora cardiaca of locust, and induction of ecdysis behaviors. Corazonin is known for its cardioactive function in cockroach and pigment modulation in locust. AKH and related peptides, grouped with red pigment concentrating hormone of crustacea are cardioacceleratory and have metabolic functions such as lipid and carbohydrate mobilization (Park, 2002b).
The present findings favor a hypothesis that the PRXa motif is an evolutionarily conserved signature in both vertebrate NMU and insect PRXa peptides. Examination of potential cross-activity of NMU and insect PRXa peptides for their receptors may provide further support for the theory of ligand-receptor coevolution in the PRXa peptide-receptor group. Another clear case of ligand-receptor coevolution has been shown for recently diverging corazonin and AKH, and their receptors (Park, 2002b).
The ligand-activated GPCR responses described in this report provide an important first step in defining authentic physiological roles for these signaling peptides. These findings help to promote a subset of GPCRs from 'orphan' to 'putative' receptors, and provide a direction for further characterization of receptors for PRXa peptides, CCAP, corazonin, and AKH. Expanded studies in Drosophila and in other insects will help to validate these initial findings (Park, 2002b).
The multiple ligand sensitivity exhibited by certain GPCRs such as CG8795 and CG6111 raises the obvious question of physiological significance. One possible interpretation is that, in contrast to a one ligand-one receptor model, certain receptors may be involved in the transduction of multiple peptide signals, thus providing a pleiotropic model of functional regulation. This possibility deserves careful examination in more physiologically relevant bioassays, as well as in vivo (Park, 2002b).
DIG-labeled antisense probes synthesized using the Ccap cDNA were used to determine the in situ pattern of expression of the gene corresponding to this cDNA in the CNS of 3rd instar larvae. The observed pattern of RNA expression matches that of the known patterns of Ccap-immunoreactivity [Ccap-IR; (Ewer, 1996)]. In Drosophila the Ccap peptide is consistently expressed in 2 pairs of neurons in the brain, 5 pairs in the subesophageal ganglion, 1-2 pairs in at least 8 ganglia of the ventral nervous system, as well as in 2 pairs of strongly immunoreactive descending axons, one lateral and one medial (see Ewer, 1996). Processing these tissues simultaneously for both RNA expression and immunoreactivity revealed that Ccap immunoreactivity and Ccap mRNA are always co-localized. This complete concordance between the two signals, coupled with the sequence information of the Ccap gene, demonstrate that the cloned sequence encodes the Ccap peptide (Park, 2003).
In Drosophila, a circadian clock controls the timing of adult emergence, with most adults eclosing between subjective dawn and late subjective morning. Although much is known about the circadian clock mechanism, comparatively little is known about how the clock regulates the expression of overt rhythmicity. The co-localization of Lark and Ccap suggests that Ccap neurons could mediate the circadian control of ecdysis, independent of its possible role in the execution of the behavior itself. To determine whether the clock directly regulates the Ccap cells, the relative locations of the clock and Ccap neuronal populations in larval and pharate adult brains were examined. This was accomplished by examining Ccap immunoreactivity in brains expressing green fluorescent protein (GFP) in the clock cell population. Using a timeless-GAL4 driver it was observed that projections from the Tim-containing DN2 neurons overlap with Ccap-immunoreactive synaptic endings in the dorsal aspect of the larval and pharate adult brains. Interestingly, DN2 neurons are postulated to be targets of Pigment dispersing factor (PDF)-containing small ventral lateral neurons (LNv), and they have been implicated in the circadian control of locomotor activity. In a separate experiment using a pdf-GAL4 driver, overlap has been demonstrated between the processes of Ccap neurons and those of tritocerebral Pdf neurons. The latter population arises post-embryonically at the mid-pupal stage, and it has been suggested that it might be involved with the circadian control of adult eclosion (Park, 2003).
Analysis of the Drosophila lark gene indicates that it encodes an RNA-binding protein that functions as a regulatory element of the circadian clock output pathway controlling adult eclosion. The Lark RNA-binding protein oscillates in abundance during the circadian cycle; importantly, the phasing of the Lark rhythm is consistent with gene-dosage studies, which indicate that the protein behaves as a repressor molecule. The Lark protein rhythm persists in constant conditions (continuous darkness and constant temperature) and is eliminated by period gene null mutations, confirming that it is under clock control and suggesting that it acts as an output mechanism that mediates the temporal regulation of adult eclosion. Lark protein oscillates in abundance within a defined group of neuropeptide (CCAP) -containing neurons of the ventral nervous system (VNS), which in other insects are thought to comprise cellular elements of the clock output pathway regulating eclosion (McNeil, 1998).
During insect metamorphosis, neuronal networks undergo extensive remodeling by restructuring their connectivity and recruiting newborn neurons from postembryonic lineages. The neuronal network that directs the essential behavior, ecdysis, generates a distinct behavioral sequence at each developmental transition. Larval ecdysis replaces the cuticle between larval stages, and pupal ecdysis externalizes and expands the head and appendages to their adult position. However, the network changes that support these differences are unknown. Crustacean cardioactive peptide (CCAP) neurons and the peptide hormones they secrete are critical for ecdysis; their targeted ablation alters larval ecdysis progression and results in a failure of pupal ecdysis. This study demonstrates that the CCAP neuron network is remodeled immediately before pupal ecdysis by the emergence of 12 late CCAP neurons. All 12 are CCAP efferents that exit the central nervous system. Importantly, these late CCAP neurons were found to be entirely sufficient for wild-type pupal ecdysis, even after targeted ablation of all other 42 CCAP neurons. Evidence indicates that late CCAP neurons are derived from early, likely embryonic, lineages. However, they do not differentiate to express their peptide hormone battery, nor do they project an axon via lateral nerve trunks until pupariation, both of which are believed to be critical for the function of CCAP efferent neurons in ecdysis. Further analysis implicated ecdysone signaling via ecdysone receptors A/B1 and the nuclear receptor ftz-f1 as the differentiation trigger. These results demonstrate the utility of temporally tuned neuronal differentiation as a hard-wired developmental mechanism to remodel a neuronal network to generate a scheduled change in behavior (Veverytsa, 2012; full text of article).
The heartbeat of adult Drosophila displays two cardiac phases, the anterograde and retrograde beat, which occur in cyclic alternation. Previous work demonstrated that the abdominal heart becomes segmentally innervated during metamorphosis by peripheral neurons that express crustacean cardioactive peptide (CCAP). CCAP has a cardioacceleratory effect when it is applied in vitro. The role of CCAP in adult cardiac function was studied in intact adult flies using targeted cell ablation and RNA interference (RNAi). Optical detection of heart activity showed that targeted ablation of CCAP neurons selectively altered the anterograde beat, without apparently altering the cyclic cardiac reversal. Normal development of the abdominal heart and of the remainder of cardiac innervation in flies lacking CCAP neurons was confirmed by immunocytochemistry. Thus, in addition to its important role in ecdysis behavior (the behavior used by insects to shed the remains of the old cuticle at the end of the molt), CCAP may control the level of activity of the anterograde cardiac pacemaker in the adult fly. Expression of double stranded CCAP RNA in the CCAP neurons (targeted CCAP RNAi) causes a significant reduction in CCAP expression. However, this reduction is not sufficient to compromise CCAP's function in ecdysis behavior and heartbeat regulation (Dulcis, 2005).
Retrograde BMP signaling in neurons plays conserved roles in synaptic efficacy and subtype-specific gene expression. However, a role for retrograde BMP signaling in the behavioral output of neuronal networks has not been established. Insect development proceeds through a series of stages punctuated by ecdysis, a complex patterned behavior coordinated by a dedicated neuronal network. In Drosophila, larval ecdysis sheds the old cuticle between larval stages, and pupal ecdysis everts the head and appendages to their adult external position during metamorphosis. This study found that mutants of the type II BMP receptor wit exhibited a defect in the timing of larval ecdysis and in the completion of pupal ecdysis. These phenotypes largely recapitulate those previously observed upon ablation of CCAP neurons, an integral subset of the ecdysis neuronal network. This study establish that retrograde BMP signaling in only the efferent subset of CCAP neurons (CCAP-ENs) is required to cell-autonomously upregulate expression of the peptide hormones CCAP, Mip and Bursicon β. In wit mutants, restoration of wit exclusively in CCAP neurons significantly rescued peptide hormone expression and ecdysis phenotypes. Moreover, combinatorial restoration of peptide hormone expression in CCAP neurons in wit mutants also significantly rescued wit ecdysis phenotypes. Collectively, these data demonstrate a novel role for retrograde BMP signaling in maintaining the behavioral output of a neuronal network and uncover the underlying cellular and gene regulatory substrates (Veverytsa, 2011).
Retrograde BMP signaling is required to maintain the behavioral output of neuronal networks. Collectively, these data show that retrograde BMP signaling upregulates the expression of a combination of peptide hormones, exclusively in the CCAP-EN subset of CCAP neurons and to a level required for those neurons to contribute to the normal execution of ecdysis behaviors. These findings in relation to the function of CCAP-ENs in ecdysis, as well as the utility of retrograde signaling as a conserved mechanism for differentiating neuronal identity and regulating behavior (Veverytsa, 2011).
A feed-forward peptide hormone cascade coordinates ecdysis. Larval and pupal pre-ecdysis is initiated by Ecdysis triggering hormone (ETH) from peripheral Inka cells stimulating Eclosion hormone (EH) secretion from brain Vm neurons. ETH and EH then act together on CCAP neurons to stimulate CCAP and Mip release. Work on the isolated Manduca central nervous system demonstrates that CCAP and MIP synergistically terminate pre-ecdysis and initiate ecdysis proper motor rhythm. This is supported by Drosophila studies; CCAP neuron ablation prolongs pre-ecdysis and ecdysis proper in larvae, and results in a deficit in the execution of the ecdysis program in pupae that reduces head and appendage eversion and extension. This role for CCAP neurons has largely been attributed to abdominal CCAP-INs acting locally on motoneurons. However, these observations indicate an essential role for BMP-dependent peptide hormone expression in CCAP-ENs. A detailed analysis of ETH-driven neuronal activity during Drosophila pupal ecdysis supports these conclusions. This study shows that T3 and A8/A9 CCAP neurons are active at the start of ecdysis proper, coincident with head eversion, and that A1-A4 CCAP neurons are active secondarily and throughout the remainder of ecdysis proper, coincident with appendage and head extension. It is suggested that the A1-A4 CCAP neurons active during pupal ecdysis proper and required for leg extension are CCAP-ENs. How would CCAP-ENs that secrete hormones into the hemolymph regulate ecdysis? It has been argued that hemolymph-borne CCAP, Mip and bursicon regulate heart rate, hemolymph pressure and cuticle expansion. However, these peptide hormones might also regulate the activity of central circuits, either indirectly or directly, as established for ETH. Genetic analysis of CCAP, Mip and bursicon peptide hormones and their receptors would provide valuable answers to these questions (Veverytsa, 2011).
CCAP-ENs require peripherally derived Gbb for BMP signaling and enhanced peptide hormone expression. CCAP-EN axons terminate on muscle 12. Muscle expresses Gbb and this study found that muscle-derived (but not neuronal-derived) Gbb significantly rescued BMP signaling and peptide hormone expression in CCAP-ENs. pMad immunoreactivity and GFP-Tkv (expressed from Ccap-GAL4) were also observed within type III boutons, indicative of local BMP signaling. Thus, together with reports that muscle-derived Gbb is sufficient for retrograde BMP signaling in motoneurons, the weight of evidence supports the somatic muscle as a primary target for Gbb access for CCAP-ENs. However, the possibility cannot be ruled out that other sources for Gbb exist, perhaps secreting the ligand into the circulating hemolymph. In this regard, it has been reported that, in gbb mutants, restoration of Gbb in another peripheral tissue, the fat body, failed to rescue BMP signaling in neurons, suggesting that distant signaling via the hemolymph is not sufficient. Further detailed analysis will be required to identify necessary and/or redundant roles for other tissues in neuronal BMP signaling (Veverytsa, 2011).
Although muscle is the likeliest target with respect to gbb, the muscle is unlikely to be the primary target for CCAP-EN peptide hormones. Ultrastructural analysis shows that type III boutons lie superficially on the muscle surface and that dense core vesicles exocytose towards the hemolymph and muscle. Furthermore, bursicon immunoreactivity is detectable in the hemolymph. CCAP-EN peptide hormones are known to target the wing, cuticle and cardiac and visceral muscle, but not the somatic muscle. This situation is unusual, as target-derived factors are typically viewed as influencing neuronal gene expression profiles pertinent to the target itself. Footpad-derived cytokines induce cholinergic differentiation of sympathetic neurons required for footpad sweat secretion. Axial differences in BMP4 ligand expression in the murine face direct subset-specific gene expression in innervating trigeminal neurons that shapes the formation of somatosensory maps. Activin and nerve growth factor in the developing skin induce expression of the hyperalgesic neuropeptide calcitonin gene-related peptide (CGRP) in nociceptive afferents (Veverytsa, 2011).
Without evidence for such a mutualistic relationship, what purpose could retrograde BMP-dependent gene expression play in CCAP-ENs? The tremendous cellular diversity of the nervous system is achieved through the progressive refinement of transcriptional cascades within increasingly diversified neuronal progenitor populations . Subsequently, retrograde signaling further differentiates the expression profile in postmitotic neurons. In such cases, unique access to extrinsic ligands allows for a certain mechanistic economy, enabling a somewhat common regulatory landscape to be adapted towards distinct gene expression profiles. In this context, it is postulated that retrograde BMP signaling functions to diversify the expression levels of peptide hormones in CCAP neurons. Drosophila interneurons and efferents can be sharply distinguished on the basis of BMP activity. Moreover, this study shows that BMP activation in CCAP-INs is capable of enhancing their peptide hormone expression, implicating a similar gene regulatory landscape in CCAP-ENs and CCAP-INs. Thus, the BMP dependence of CCAP, Mip and Bursß offers a simple solution to the problem of how to selectively enhance peptide hormone expression in CCAP-ENs (Veverytsa, 2011).
BMP signaling offers an additional advantage to neuronal diversification. Studies of axial patterning in Drosophila have unveiled a wealth of mechanisms that diversify and gauge transcriptional responses to BMP signaling. These mechanisms revolve around the outcome of pMad/Medea activity at a gene's cis-regulatory sequence, as influenced by their affinity for specific cis-regulatory sequences and local interactions with other transcription factors, co-activators and co-repressors. As a result, pMad/Medea activity can be extensively shaped to generate gene- and cell-specific responses and determine whether genes are on or off or up- or downregulated. This flexibility is likely to underpin the differential sensitivity of CCAP, Mip and Bursß to a common retrograde BMP signal within a single cell, as well as the utility of BMP signaling as a common retrograde regulator of subset-specific gene expression in distinct neuronal populations (Veverytsa, 2011).
Finally, the differential regulation of Bursα and Bursβ is intriguing because they are believed to only function as a heterodimer. Although the possibility of functional homodimers cannot be discounted, it is postulated that the selective BMP dependence of Bursβ might be an efficient mechanism for modulating the activity of the active bursicon hormone. This would be analogous, and perhaps orthologous, to the regulation of follicle-stimulating hormone in mammals. Its cyclical upregulation during the oestrous cycle is dictated by the regulation of only one of its subunits, FSHβ, by the TGFβ family ligand activin (Veverytsa, 2011).
Numerous studies have described the impact of retrograde signaling on neuronal network formation and function. During spinal sensory motor circuit development, retrograde neurotrophin signaling induces specific transcription factor expression in motoneurons and Ia afferents that is required for appropriate motor sensory central connectivity, which, when inoperative, results in ataxic limb movement. Similarly, murine trigeminal neurons utilize spatially patterned BMP4 expression in the developing face to target their centrally projecting axons in a somatotopically appropriate manner. Retrograde signaling also modulates physiologically responsive neuronal gene expression. In vertebrates, skin injury induces cutaneous activin and nerve growth factor expression, which retrogradely upregulates sensory neuron expression of CGRP, which mediates hyperalgesia. In sensory motor circuits of Aplysia, retrograde signals are required to upregulate presynaptic sensorin, a neuropeptide required for long-term facilitation of the sensorimotor synapse (Veverytsa, 2011).
The current evidence suggests that the function of BMP signaling is not mediated within a specific developmental window, but is required on an ongoing basis. The Ccap-GAL4 transgene is not active until late larval stage L1, after CCAP neuron network assembly and peptide hormone initiation. Yet, wit phenotypes were significantly rescued using Ccap-GAL4. Together with observation of persistent pMad immunoreactivity in CCAP-ENs, it is concluded that BMP signaling acts permissively to maintain the capacity of CCAP-ENs to contribute to ecdysis, rather than acting phasically at ecdysis to instructively activate ecdysis behaviors or enable CCAP-ENs to contribute. Such a maintenance role is supported by previous work showing that maintained expression of the neuropeptide FMRFa requires persistent retrograde BMP signaling. It was also found that type III synapses on muscle 12 have significantly fewer boutons and shorter branches in wit mutants, implicating a role for BMP signaling in CCAP-EN synaptic morphology, as first described for type I neuromuscular junctions in wit mutants. It will be of interest to investigate whether dense core vesicle exocytosis is also perturbed in wit mutants, akin to the reduced synaptic vesicle exocytosis at type I boutons in wit mutants (Veverytsa, 2011).
To produce animals lacking Ccap neurons, expression of the cell death gene reaper (rpr) was driven in Ccap neurons, using the Ccap-GAL4 transgenic strain. A similar approach has been successfully used to study the function of other Drosophila neuropeptides and hormones. To investigate the consequences of loss of Ccap neurons on larval ecdysis, Ccap neurons had to be absent, at the latest, prior to the last larval ecdysis (from 2nd to 3rd larval instar). The targeted expression of rpr using the Ccap-GAL4 driver was shown to produce late 2nd instar larvae that are probably entirely devoid of Ccap function. In certain experiments that examined post-larval ecdyses, animals were transferred to 20°C after collection as first instar larvae and raised at this temperature until pupation or eclosion. At this lower temperature the vast majority of the CNSs was also mostly devoid of Ccap neurons by the end of the 3rd instar (at wandering). Thus, of 22 CNSs examined at this time, 15 showed no Ccap- or ß-gal-immunoreactive neurons or processes, while four, two and one CNSs had one, two and four weakly stained neurons, respectively, and none of these CNSs had visible immunoreactive processes. When the CNS of animals raised using the eclosion rhythm paradigm (25°C to 18°C) was processed for Ccap- and ß-gal-IR immediately after adult eclosion, 25 of 28 CNSs showed no immunoreactivity, while two and one CNSs had one and two weakly staining neurons, respectively, lacking visible processes (Park, 2003).
In the moth Manduca sexta, addition of CCAP to an isolated larval abdominal CNS turns on the ecdysis motor program (Gammie, 1997b; Zitnan, 2000). This, and other evidence (reviewed by Ewer, 2002), strongly implicates the CCAP neuropeptide in the control of ecdysis behavior in this moth. In the CNS of Drosophila larvae, Ccap-IR decreases shortly before the onset of larval ecdysis, suggesting that Ccap is similarly important for the control of ecdysis in this insect (Park, 2003).
In Drosophila, there are two larval intermolts, the intermolt between first and send larval instars, and the intermolt between second and third instars. To investigate directly the role of Ccap in larval ecdysis, animals lacking the Ccap neuronal population were characterized. Surprisingly, it was found that genetic ablation of the Ccap neurons is not lethal during the larval stages. Indeed, the survival rate of Ccap-KO from 1st instar to the end of the 3rd (last) instar is indistinguishable from that of the control population (97% vs. 95%, respectively). This indicates that Ccap is not essential for viability during (at least) the latter part of the 2nd larval intermolt period and the entire 3rd larval instar. Most significantly, animals lacking Ccap neurons were able to shed their old cuticle at the end of molt to the 3rd instar. Independent studies show that animals homozygous for small chromosomal deletions including Ccap (and 14 other genes) survive until the 3rd instar. Thus, survival of Ccap-KO larvae until this stage is not due to persisting (but immunohistochemically undetectable) Ccap peptide (Park, 2003).
To determine whether ecdysis behavior is normal in KO animals, the sequence and timing of ecdysis behavior from the 2nd to the 3rd instar was examined. The earliest obvious marker for the impending ecdysis is the appearance of pigmentation in the mouth plates of the future 3rd instar (double mouth plates stage; DMP), which occurs about 30 minutes before ecdysis. Approximately 16 minutes after the DMP stage, air enters the new trachea; this is followed shortly by the onset of the preparatory behavior called pre-ecdysis ( Park, 2002a). Approximately 15 minutes after air filling, pre-ecdysis stops and the animal executes a characteristic 'biting' behavior during which it appears to be attempting to tear the anterior region of the old cuticle. This period is then followed by the onset of ecdysis proper, which is characterized by vigorous peristaltic waves sweeping along the animal in a posterior-to-anterior direction. Typically after three to four waves, the anterior cuticle breaks, freeing the 3rd instar of its 2nd instar cuticle. After a period of a few minutes the animal resumes feeding and locomotory behavior (Park, 2003).
Although the Ccap-KO larvae are clearly able to initiate ecdysis behavior and use this behavior to free themselves from the 2nd instar cuticle, there are subtle but significant differences between the behavior of Ccap-KO and control animals. The duration of events up to the onset of pre-ecdysis is indistinguishable for these two groups of larvae. The first notable difference between Ccap-KOs and control larvae is a modest but significant lengthening of pre-ecdysis behavior, although pre-ecdysis behavior itself appears normal (Park, 2003).
Additionally, the subsequent events that lead to cuticle shedding takes approx. three times longer in Ccap-KO larvae than in controls. Both the biting period, which occurs between the end of pre-ecdysis and ecdysis onset, and the duration of ecdysis itself, are significantly extended in Ccap-KO animals. Interestingly, Ccap-KO larvae exhibit anterior to posterior peristaltic waves interspersed with the typically occurring posterior to anterior waves, a behavior never observed in control animals. Because the waves moving in the anterior to posterior direction do not aid in breaking the old cuticle, the time to successful shedding of the old cuticle is lengthened (Park, 2003).
These results reveal that the ablation of Ccap neurons is associated with defects that are strictly confined to the execution of ecdysis itself. Thus, while the entire duration of the period between DMP and ecdysis is increased by only 14%, from the normal 31.9±1.0 minutes to 36.3±0.9 minutes, the timing and organization of ecdysis behavior itself is quite severely disrupted in the KO animals (Park, 2003).
In higher Diptera such as Drosophila , pupal ecdysis (pupation) corresponds to the behavior referred to as 'head eversion'. During head eversion, the brain, which in the larva is located behind the mouthparts, is pushed anteriorly to a position in front of the thorax and the mouthparts. At the same time, the appendages, which were formed from the eversion of the imaginal discs at pupariation (the onset of the larval-pupal transition), are extended to attain their final size and shape (Park, 2003).
In contrast to the situation observed in the larva, most Ccap-KO animals die during the pupal stage. Furthermore, the appearance of KO animals at the end of pupation and of metamorphosis suggests that the primary cause of their death is a specific failure of pupal ecdysis. Indeed, in KO pupae and pharate adults, the head is located much more to the anterior than normal or is only partially everted; the larval tracheae have not been completely shed; and the appendages have not been properly extended, resulting in a pharate adult that has abnormally short wings and legs (Park, 2003).
In order to determine the bases for these defects, the timecourse of pupal ecdysis was examined in KO animals. In Drosophila , pupation occurs approx. 12 hours after pupariation. Pupal ecdysis is preceded by a preparatory behavior (termed here pre-ecdysis by analogy to the corresponding larval behavior), during which the posterior part of the animal rhythmically retracts from the puparium. About 9-10 minutes after the onset of pre-ecdysis, a short succession of peristaltic waves sweeps from the posterior to the anterior of the animal and causes the eversion of the head, the shedding of the larval tracheae, and a rapid extension of the appendages. Head eversion is followed by a long post-ecdysis period of several hours during which regular contractions, primarily of the abdomen, occur; this presumably aids in giving the insect its final form (Park, 2003).
Ccap-KO animals initiate normal pre-ecdysis behavior (for instance the frequency of abdominal 'sweeps' is the same as in controls). However, this behavior lasts significantly longer than in controls and is not followed by head eversion. Instead, abdominal pre-ecdysis movements eventually cease during a final retraction and are followed by a period that resembles the postecdysis period seen in the control (but which is significantly shorter in Ccap-KO animals (Park, 2003).
Although the KO pre-pupae all lack Ccap neurons, the morphological phenotype seen at the end of metamorphosis is somewhat variable, with, for instance, a variable amount of the adult head visible at the end of adult development. However, all flies show shortened appendages, and all animals whose pupation behavior was observed in detail show no pupal ecdysis. The basis for this variable phenotype is currently unknown (Park, 2003).
If head eversion is stimulated by Ccap, the neuropeptide should be released at this time. Indeed, in wild type animals, a substantial decrease in Ccap-IR is detected following pupation in descending Ccap immunopositive axons. The slight increase in the number of Ccap-immunoreactive varicosities that is apparent at the start of pre-ecdysis is a reflection of a subtle fragmentation in the pattern of Ccap-IR that is seen at this time, and may be the first sign that Ccap has started to be released. The ETH peptides are known to be essential for larval pre-ecdysis in Drosophila (Park, 2002a), and the drop in ETH-IR that is observed at the onset of pupal pre-ecdysis suggests that these peptides may also control this behavior at pupation (Park, 2003).
The KO animals that formed relatively normal heads at the end of metamorphosis are usually able to exit from the pupal case. A careful examination of eclosion has shown that the developmental and behavioral events that take place at this time occurs in the correct sequence in Ccap-KO animals, although some quantitative differences in the duration or number of events are observed. Thus, while tracheal filling occurs before the start of the eclosion behaviors, in Ccap-KO animals it takes longer than in controls. However, the ptilinum, which is used to rupture the anterior of the pupal case, is deployed normally at the expected time. Finally, and most significantly, the bouts of rapid anteriorly directed peristalses of ecdysis proper occurred in the KO animals. Interestingly, however, these bouts are relatively ineffective at propelling the animal forward. This is not due to a difference in the characteristics of the bouts themselves, which careful cinematographic analyses shows are very similar to those of control animals. Instead, this failure occurred because the abdomen of KO animals is not distended at this time, severely reducing the traction exerted by the body on the inner walls of the pupal case: this is needed in order for the abdominal peristalses to cause the rapid net forward movement that is seen in control animals. Although most KO animals (nine out of 10 examined) eventually succeeded in eclosing, extrication took much longer than normal. Thus, unlike larval and pupal ecdysis, the actual ecdysis motor program of the adult appears to be relatively normal in KO animals (however, the frequency of peristalses is lower than in controls, even when the two groups are compared during the first minute after the onset of eclosion, which corresponds approximately to the duration of eclosion in controls. Therefore, the most dramatic deficiency of Ccap-KO animals at eclosion appears to be due to the absence of a function required to expand the body rather than to a failure in the adult ecdysis motor program itself (Park, 2003).
The phenotypes of adult Ccap-KO flies suggest that Ccap neurons play some role in post-eclosion events. KO adults do not inflate their wings, and their cuticle appears to remain soft and untanned, as evidenced by the dimpling that is observed on the dorsal thorax at sites of thoracic muscle insertion. The defect in wing expansion may be due, in part, to the failure in wing extension at the time of pupation (Park, 2003). The tanning defect of the KO flies may occur because a subset of the Ccap neurons expresses the gene encoding the tanning hormone, bursicon (E. Dewey and H. W. Honegger, personal communication to Park, 2003).
In another experiment, the Ccap-GAL4 driver was used to overexpress a temperature-sensitive form of shibire (shi; the fly dynamin homolog) in the CCAP cell population (using a UAS-shits transgene). When reared at 29°C, progeny carrying both the Ccap-GAL4 and UAS-shits transgenes exhibited defects in wing expansion ~80%-100% of the populations), whereas control progeny (with only one transgene) have normal wings. At 25°C, both types of progeny have normal wings, indicative of a temperature-sensitive effect (Park, 2003).
To examine circadian rhythms of eclosion, Ccap-KO and control animals were reared under conditions that produced the maximal number of pharate adults, and then adult emergence was scored at two-hour intervals over the course of several days, both under a light:dark cycle (LD 12:12) and in constant darkness (DD). In three separate experiments using one Ccap-GAL4 line and in two separate experiments using a second independent transgenic line, a clear rhythmicity was observed under both LD and DD conditions, with most of the animals eclosing in the dawn-early morning (or subjective dawn-early morning) interval. Nevertheless, there were differences between the eclosion profiles of KO and control populations. Most notably, the temporal gate of eclosion was lengthened in KO animals, with significant emergence occurring in the late night/predawn period. Coupled with this wider eclosion 'gate', a significant diminution was observed in the amplitude of the eclosion burst that occurs immediately following lights-on, which in control populations constitutes approximately 40% of the flies that emerge on any given day. No consistent difference in the peak time of eclosion was observed between KO and control populations in LD or DD conditions (Park, 2003).
A neuropeptide hormone-signalling pathway controls events surrounding eclosion in Drosophila. Ecdysis-triggering hormone, eclosion hormone and crustacean cardioactive peptide (CCAP) together control pre-eclosion and eclosion events, whereas bursicon, through its receptor rickets (RK), controls post-eclosion development. Cuticular tanning is a convenient visible marker of the temporally precise post-eclosion developmental progression, and this study investigated how it is controlled by the ecdysis neuropeptide cascade. Together, two enzymes, tyrosine hydroxylase (TH, encoded by ple) and dopa decarboxylase (DDC, encoded by Ddc), produce the dopamine that is required for tanning. Levels of both the ple and Ddc transcripts begin to accumulate before eclosion, coincident with the onset of pigmentation of the pharate adult bristles and epidermis. Since DDC activity is high before the post-eclosion onset of tanning, a different factor must be regulated to switch on tanning. Transcriptional control of ple does not regulate the onset of tanning because ple transcript levels remain unchanged from 24 hours before to 12 hours after eclosion. TH protein present before eclosion is degraded, and no TH activity can be detected at eclosion. However, TH protein rapidly accumulates within an hour of eclosion, and evidence is provided that CCAP controls this process. Furthermore, TH is shown to be transiently activated during tanning by phosphorylation at Ser32, as a result of bursicon signalling. It is concluded that the ecdysis hormone cascade acts as a regulatory switch to control the precise onset of tanning by both translational and activational control of TH (Davis, 2007).
In Drosophila, the onset of tanning of the puparium occurs within 1 hour after the wandering larva becomes sessile. This requires metabolites of DA, the production of which is dependent on the actions of TH and DDC. Transcripts levels of both genes, and TH protein and activity levels, are all high in white pre-pupae (WPP). Unlike at eclosion, TH does not appear to be activated by PKA phosphorylation for the rapid tanning of the pupal case at pupariation. This is not unexpected because the ecdysis neuropeptides are not released until a full 12 hours APF. During the late third instar, the relatively insoluble tyrosine, which is indispensable for tanning, is stored as a more soluble derivative, tyrosine-O-phosphate (tyr-P). Tanning at pupariation is probably controlled by the release of tyrosine from tyr-P. No appreciable accumulation of tyr-P occurs before eclosion, suggesting that post-eclosion tanning is switched on by a different mechanism (Davis, 2007).
This study establishes a role for the ecdysis neuropeptide cascade in post-eclosion tanning by examining the regulation of two genes, ple and Ddc, which encode two enzymes with critical roles in tanning. Semi-quantitative RT-PCR was used to examine the profile of transcription after puparium formation. Levels of both transcripts are high in WPP, but they drop and then rise again before eclosion. Ddc levels begin to increase 60 hours APF, reach their peak 84 hours APF, and decline thereafter. DDC enzyme activity is required before eclosion for pigmentation of the pharate adult bristles and epidermis and after eclosion for tanning of the adult cuticle, and reaches a peak at eclosion. This indicates that Ddc is transcribed and translated before eclosion to ensure enzyme activity is present when substrate becomes available. This study investigated whether the control of substrate availability, and therefore the control of tanning, is effected by the transcriptional, translational, or post-translational regulation of TH (Davis, 2007).
Levels of ple transcripts are high during the 24 hour period spanning eclosion. The early appearance of ple transcripts is not surprising, because pigmentation of the pharate adult bristles and epidermis occurs between 84 and 96 hours APF. Both ple (and Ddc) transcription are normal in EH-KO, CCAP-KO, bursZ1091 and rk4 flies. The accumulation of ple transcripts before eclosion, the maintenance of high levels of TH transcription until 12 hours after eclosion and the fact that neuropeptide mutant and ablation knockout flies exhibit normal ple transcription, led to the conclusion that the precise onset of tanning following eclosion is not due to regulation of ple transcription (Davis, 2007).
TH protein and activity levels are high before eclosion when pigmentation of the pharate adult bristles and epidermis occurs. Levels fall rapidly just before eclosion and rise thereafter. During this entire time, ple transcripts are present, suggesting that protein levels are being regulated. The drop in TH protein levels may occur through repression of translation from ple transcripts and/or increased turnover of the protein. The complete failure of CCAP-KO flies to accumulate TH protein following eclosion, although they transcribe ple normally, indicates a role for CCAP in this process. This could occur at the level of translation; alternatively, CCAP signalling may alter TH protein stabilisation. Since PKA signalling has been shown to regulate proteins involved in translational control, it is more likely that CCAP signalling activates PKA to cause translation, not stabilisation, of TH following eclosion (Davis, 2007).
EH-KO, bursZ1091 and rk4 flies all appear to have relatively normal TH protein and activity profiles. Although all three exhibit a considerable range of activity in WPP, the pupal cases of these organisms tan normally. Despite the initial delay in TH accumulation in EH-KO flies following eclosion, these flies, and bursZ1091 and rk4 mutants, maintain high levels of TH until 144 hours APF, a time when TH is undetectable in control flies. This persistence of TH indicates a delay in the execution of the neuropeptide hormone cascade. Interestingly, rk4 flies also show a delay in degradation of TH following pupariation. Perhaps there is a requirement for RK signalling to trigger TH degradation following tanning of the puparium (Davis, 2007).
Neck-ligation of flies at eclosion prevents tanning, whereas flies ligated 30 minutes after eclosion tan normally. Furthermore, tanning of flies neck-ligated at eclosion is rescued by injection of 8-Br-cAMP. TH protein begins to accumulate 1 hour after eclosion in control flies. Phosphorylation of the protein by PKA at Ser32 leads to enzyme activity rising between 1.5 and 3 hours after eclosion. It is concluded that the translational and activational state of TH is responsible for controlling tanning following eclosion. TH protein accumulates, but is not phosphorylated in flies neck-ligated at eclosion resulting in reduced TH activity. Interrupting neuropeptide signalling after eclosion reveals that the element that controls TH translation is released before eclosion. The loss of TH accumulation in CCAP-KO flies and the restoration of TH accumulation upon injection of CCAP suggests that CCAP is responsible for inducing TH translation (Davis, 2007).
Flies neck-ligated 30 minutes after eclosion, translate and phosphorylate TH normally. By allowing neuropeptide signalling after eclosion, it has been demonstrated that a factor is released within 30 minutes of eclosion that causes phosphorylation and therefore activation of TH. The reduced phosphorylation of Ser32 in bursZ1091 flies, and complete loss of phosphorylation in rk4, bursZ1091/bursZ5569 and rk1/rk4 flies suggests that bursicon signalling through RK controls this process. Activity levels of TH are significantly reduced in flies neck-ligated at eclosion compared with control flies. Flies ligated 30 minutes after eclosion show twofold higher levels than flies neck-ligated at eclosion and this difference probably accounts for the presence or absence of tanning. This suggests that a critical threshold of TH activity exists that is surpassed in the flies ligated at 30 minutes. Thus, although the activity present in these flies is significantly less than that in control flies, the organisms have sufficient TH activity to tan, whereas flies ligated at eclosion do not attain the threshold of activity required for tanning. Injection of 8-Br-cAMP into flies neck-ligated at eclosion rescues tanning by restoring phosphorylation and therefore activation of TH. Although injection of 8-Br-cAMP does not restore TH activity to control levels, it increases activity nearly sixfold, achieving the threshold of activity required for tanning following eclosion (Davis, 2007).
These results, taken together, suggest that at least two factors control the precise timing of tanning after eclosion. One, released before eclosion, causes translation of TH; the other, released after eclosion, causes phosphorylation and activation of TH. Both EH and CCAP are released before eclosion to control pre-ecdysis and ecdysis, respectively. EH-KO and CCAP-KO flies both exhibit extreme post-eclosion tanning defects. EH-KO flies take more than 9 hours to tan and CCAP-KO flies fail to tan. TH protein is undetectable in EH-KO flies immediately following eclosion, but these flies do eventually accumulate TH and tan. The complete failure of CCAP-KO flies to tan, combined with the fact that CCAP-KO flies fail to accumulate TH from the ple transcripts that are present at eclosion, suggest that CCAP is responsible for inducing TH translation. The initial failure of EH-KO flies to accumulate TH is probably caused by a failure to trigger the rapid release of CCAP. Presumably, enough CCAP is eventually released in these flies to effect the translation of TH and eventually tanning, because the EH genetic ablation is leaky. Consistent with this prediction, EH-KO flies that expand their wings accumulate TH normally, suggesting that CCAP is released normally in these flies. TH translation is restored in CCAP-KO flies injected with CCAP and rescue of TH accumulation and phosphorylation occurs when EH-KO and CCAP-KO flies are injected with 8-Br-cAMP. Rescue of both defects probably occurs because injection of 8-Br-cAMP activates PKA in CCAP target cells, thus circumventing the need for CCAP release, and also activates PKA in TH-expressing cells, leading to phosphorylation and activation of TH (Davis, 2007).
These data suggest that the post-eclosion factor causing the phosphorylation of Ser32 is the heterodimeric hormone bursicon. It is responsible for tanning and wing expansion and acts through its receptor RK. Consistent with the role of bursicon in the phosphorylation of TH, rk4 flies fail to phosphorylate TH and have reduced activity. These flies show a delay in tanning, taking up to 9 hours to tan. Injection of 8-Br-cAMP rescues tanning by restoring phosphorylation and therefore activation of TH (Davis, 2007).
Two mutants in the α subunit of bursicon have been identified, of which one (bursZ5569) shows a delay in tanning in 40% of the progeny, whereas a delay is present in 82% of bursZ1091/bursZ5569 flies. The bursZ1091 mutant does not show a delay in tanning, although phosphorylation of TH is reduced in these flies. Phosphorylation of Ser32 is undetectable in bursZ1091/bursZ5569 flies, probably causing the more severe tanning defect seen in these flies. The reduced phosphorylation of TH in bursZ1091 flies corresponds to a minor loss of TH activity. Thus, it seems that the threshold TH activity required for proper tanning is achieved in bursZ1091 flies, although they do not have wild-type levels of TH phosphorylation or activity. Normal tanning in these flies cannot be attributed to residual activity of the β subunit of bursicon, CG15284, proposed to be encoded by pu (S. McNabb and J. Truman, personal communication to Davis, 2007), because neither subunit independently confers bursicon activity. The bursZ1091 allele is probably a hypomorph, and creation of a null allele would be useful. Additional studies on the activational state of TH in pu or burs null mutants will help to elucidate why tanning is not delayed in bursZ1091 flies (Davis, 2007).
The data indicate that CCAP is responsible for initiating TH translation following eclosion. In Drosophila, translational regulation often occurs through microRNA (miRNA)-dependent RNAi-mediated repression through binding sites in the 3'UTR of transcripts. Three miRNAs - let-7, mir-iab-4-3p and mir-iab-4-5p - have been predicted to regulate TH translation in Drosophila. It is conceivable that one or more of these miRNAs, in association with the RISC complex, could bind to ple transcripts to cause the repression of translation through a miRNA-dependent RNAi-mediated mechanism. It is also plausible that PKA, activated by CCAP signalling, might relieve repression of TH translation by phosphorylation of one of the subunits of the RISC complex or associated proteins. Future work will establish whether there is a role for these miRNAs in the repression of TH translation before eclosion (Davis, 2007).
Ecdysis behavior allows insects to shed their old exoskeleton at the end of every molt. It is controlled by a suite of interacting hormones and neuropeptides, and has served as a useful behavior for understanding how bioactive peptides regulate CNS function. Previous findings suggest that crustacean cardioactive peptide (CCAP) activates the ecdysis motor program; the hormone bursicon is believed to then act downstream of CCAP to inflate, pigment, and harden the exoskeleton of the next stage. However, the exact roles of these signaling molecules in regulating ecdysis remain unclear. This study used a genetic approach to investigate the functions of CCAP and bursicon in Drosophila ecdysis. Null mutants in CCAP were shown to express no apparent defects in ecdysis and postecdysis producing normal adults. By contrast, a substantial fraction of flies genetically null for one of the two subunits of bursicon [encoded by the partner of bursicon gene (pburs)] show severe defects in ecdysis, with escaper adults exhibiting the expected failures in wing expansion and exoskeleton pigmentation and hardening. Furthermore, flies lacking both CCAP and bursicon show much more severe defects at ecdysis than do animals null for either neuropeptide alone. The results show that the functions thought to be subserved by CCAP are partially effected by bursicon, and that bursicon plays an important and heretofore undescribed role in ecdysis behavior itself. These findings have important implications for understanding the regulation of this vital insect behavior and the mechanisms by which hormones and neuropeptides control the physiology and behavior of animals (Lahr, 2012).
The fragmentary understanding of the regulation of ecdysis behavior indicates that it is controlled by a suite of neuropeptides and hormones that show complex hierarchical and reciprocal relationships, and in which a given neuropeptide (or hormone) may act on different targets or act in a combinatorial manner on a specific target with other neuropeptides (or hormones). This study isolated mutants null for CCAP and pburs to better define the functions of these genes and to investigate possible synergistic actions. It was surprising to find that animals lacking CCAP expressed normal pupal ecdysis behavior because CCAP is believed to be the key neuropeptide that controls ecdysis. For instance, application of CCAP to an isolated Manduca CNS will turn on the ecdysis motor program. Also, RNA interference (RNAi) of CCAP or its receptor, CCAPR-2, by injection of double-stranded RNA, causes arrest at ecdysis in Tribolium. Furthermore, because bursicon has previously only been associated with the regulation of postecdysis events following adult eclosion, it was were also surprising to discover that pburs-null mutants showed severe defects at pupation. Nevertheless, RNAi of both bursicon subunits as well as of its receptor (rickets, rk) cause a quantitative weakening of preecdysis behavior in Tribolium, and release of bursicon during Drosophila pupal preecdysis has recently been reported, suggesting a role in the control of early phases of the ecdysis sequence. Furthermore, it has been reported that interference of rk function in Drosophila causes defects at pupation, although the range of additional nonecdysial defects observed suggest that such manipulations interfered with other pathways, rendering the interpretation of these findings more difficult. In this regard, the results using animals mutant for pburs indicate that PBURS plays an important role, and that this role is primarily restricted to the correct execution of ecdysis behaviors (a role in postecdysis has not been investigated at this stage). A role for bursicon specifically at pupal ecdysis was recently uncovered by showing that defects at pupation, caused by the elimination of the retrograde signal needed for CCAP and PBURS expression in the CNS, could be partially rescued by specifically restoring pburs expression in the relevant neurons (Veverytsa, 2011; Lahr, 2012).
Although flies lacking CCAP were ostensibly entirely normal, it was possible to uncover a critical function for this peptide at ecdysis by examining pupation in animals lacking pburs function. Indeed, in this mutant background, eliminating CCAP caused an almost complete failure of ecdysis. This suggests that both CCAP and PBURS regulate ecdysis, with CCAP playing a minor role and PBURS playing a major role. The bases of CCAP and bursicon actions, however, remains unclear. The CCAP-expressing neurons in the ventral CNS consist of a pair of efferent neurons in segments T3-A4; homologous to cell 27s in other insects, and a pair of interneurons (CCAPIN) in segments T1-A9; homologous to IN704 in other insects. In Manduca, addition of CCAP to an isolated CNS can activate and sustain the ecdysis motor program. The limited arborization of CCAPE within the CNS would imply that this activational role would be subserved by CCAPIN, and is consistent with the type of role that these neurons play after adult emergence; by contrast, CCAPE neurons release bursicon into the hemolymph to first plasticize then harden and melanize the wings and exoskeleton, and play no behavioral role. Alternatively, the activation of ecdysis could be mediated by a pair of CCAP neurons in the subesophageal ganglion (SEG). At least at adult emergence, it is these neurons that command postecdysial behaviors, such as air-swallowing and wing inflation. However, both CCAP neurons in the SEG and the CCAPINs express CCAP but not PBURS, and no ecdysial defects were detected in CCAP-null mutants. By contrast, recent findings show that reducing CCAP and bursicon expression from CCAPEs causes severe defects in pupation, implying that these neurons may be key for the activation of ecdysis behavior. Since CCAPEs have a sparse arborization within the CNS, these results would also imply that the activational roles of CCAP and bursicon could be indirect (Lahr, 2012).
While pupation requires activation of motor programs, changes in hemolymph pressure may also be essential for correct eversion of the head and the proper extension of legs and wings. Thus, it is also possible that CCAP's role in Drosophila ecdysis is at least in part based on its cardioactive function, instead of or in addition to a neural activation role. Indeed, CCAP is cardioactive in insects including Drosophila and, in addition to serving to better disperse coreleased neuropeptides and neurohormones, including bursicon, this cardioactive function may be necessary for the successful transformation into a pupa. The identification of the direct targets of CCAP and bursicon coupled with functional studies will be needed for the full understanding of the exact roles that these peptides play at pupation (Lahr, 2012).
Independent of the exact nature of their functions, the actions of CCAP and bursicon show the hallmark complexity of neuropeptide control of physiology and behavior. In addition to each of these molecules acting on different targets (e.g., bursicon, which activates ecdysis and also causes wing inflation and the hardening and pigmentation of the adult exoskeleton), it was shown that CCAP and bursicon act synergistically to control ecdysis behavior. Such convergence is seen in a number of peptide systems, and appears to be the basis for the integration of multiple signals and many time-independent signals. Such a situation occurs, for example, in the control of arousal, which depends on inputs related to food intake and satiation, as well as from inputs from the circadian clock. Another role for multiple peptidergic inputs may be to increase the precision and robustness of a response. For example, mammalian circadian clocks cause daily rhythms of locomotor activity to be expressed with a precision of ~1 min/d. The basis for this precision is not entirely understood, but is likely mediated by the action of multiple clock output neuropeptides, all of which can affect the pattern of activity/inactivity. Ecdysis likewise shows a very precise timing, and naturally occurring failures are extremely rare. Although this study has shown that CCAP is not essential for ecdysis in the laboratory, it may nevertheless provide a signal that, under particular conditions, is essential for the successful and seamless execution of the behavior. This signal may also vary in different insects, reflecting a bias toward one of several possible actions in organisms with different body plans. Thus, for instance, CCAP may primarily play a cardioactive role in some insects, whereas for others it may play a critical role in activating a motor program itself. It is hoped that future comparative work using insects with different developmental and anatomical constraints will help elucidate the logic behind such biases. In addition to such an approach, work in Drosophila and Tribolium has clearly shown that molecular genetics provides a unique tool to understand the essential as well as the redundant functions of every ecdysis neuropeptide and hormone. The combination of both approaches will shed light on the mechanism that enables insects to flawlessly complete a complex behavioral sequence almost regardless of conditions. It will also provide a useful model for understanding how neuropeptides control the physiology and behavior of all animals (Lahr, 2012).
Arakane, Y., Li, B., Muthukrishnan, S., Beeman, R. W., Kramer, K. J. and Park, Y. (2008). Functional analysis of four neuropeptides, EH, ETH, CCAP and bursicon, and their receptors in adult ecdysis behavior of the red flour beetle, Tribolium castaneum. Mech. Dev. 125(11-12): 984-95. PubMed Citation: 18835439
Baker, J. D., McNabb, S. L. and Truman, J. W. (1999). The hormonal coordination of behavior and physiology at adult ecdysis in Drosophila melanogaster. J. Exp. Biol. 202: 3037-3048. 10518485
Brody, T. and Cravchik, A. (2000). Drosophila melanogaster G protein-coupled receptors. J. Cell Biol. 150: F83-F88. 10908591
Cheung, C. C., Loi, P. K., Sylwester, A. W., Lee, T. D. and Tublitz, N. J. (1992). Primary structure of a cardioactive neuropeptide from the tobacco hawkmoth, Manduca sexta. FEBS Lett. 313(2): 165-8. 1426284
Chung, J. S., Dircksen, H. and Webster, S. G. (1999). A remarkable, precisely timed release of hyperglycemic hormone from endocrine cells in the gut is associated with ecdysis in the crab Carcinus maenas. Proc. Natl. Acad. Sci. 96: 13103-13107. 10557280
Davis, M. M., et al. (2007). A neuropeptide hormone cascade controls the precise onset of post-eclosion cuticular tanning in Drosophila melanogaster. Development 134: 4395-4404. PubMed Citation: 18003740
Davis, N. T., Homberg, U., Dircksen, H., Levine, R. B. and Hildebrand, J. G. (1993). Crustacean cardioactive peptide-immunoreactive neurons in the hawkmoth Manduca sexta and changes in their immunoreactivity during postembryonic development. J. Comp. Neurol. 338: 612-627. 8132864
Dircksen, H. (1998). Conserved crustacean cardioactive peptide (CCAP) neuronal networks and functions in arthropod evolution. In: Recent advances in Arthropod Endocrinology, vol. 65 (ed. G. M. Coast and S. G. Webster), pp. 302-333. Cambridge: Cambridge University Press.
Donini, A. and Lange, A. B. (2002a). The effects of crustacean cardioactive peptide on locust oviducts are calcium-dependent. Peptides 23(4): 683-91. 11897387
Donini, A., Ngo, C. and Lange, A. B. (2002b). Evidence for crustacean cardioactive peptide-like innervation of the gut in Locusta migratoria. Peptides 23(11): 1915-23. 12431729
Dulcis, D., Levine, R. B. and Ewer, J. (2005). Role of the neuropeptide CCAP in Drosophila cardiac function. J. Neurobiol. 64: 259-274. 15898062
Ewer, J. and Truman, J. W. (1996). Increases in cyclic 3',5'-guanosine monophosphate (cGMP) occur at ecdysis in an evolutionarily conserved crustacean cardioactive peptide-immunoreactive insect neuronal network. J. Comp. Neurol. 370: 330-341. 8799859
Ewer, J. and Truman, J. W. (1997). Invariant association of ecdysis with increases in cyclic 3',5'-guanosine monophosphate (cGMP)-immunoreactivity in a small network of peptidergic neurons in the hornworm, Manduca sexta. J. Comp. Physiol. 181: 319-330. 9342855
Ewer, J. and Reynolds, S. (2002). Neuropeptide control of molting in insects. In: Hormones, brain and behavior, vol. 35 (ed. D. W. Pfaff, A. P. Arnold, S. E. Fahrbach, A. M. Etgen and R. T. Rubin), pp.1-92. San Diego, CA: Academic Press.
Gammie, S. C. and Truman, J. W. (1997a). An endogenous elevation of cGMP increases the excitability of identified insect neurosecretory cells. J. Comp. Physiol. A 180: 329-337. 9106996
Gammie, S. C. and Truman, J. W. (1997b). Neuropeptide hierarchies and the activation of sequential motor behaviors in the hawkmoth, Manduca sexta. J. Neurosci. 17: 4389-4397. 9151755
Gammie, S. C. and Truman, J. W. (1999). Eclosion hormone provides a link between ecdysis-triggering hormone and crustacean cardioactive peptide in the neuroendocrine cascade that controls ecdysis behavior. J. Exp. Biol. 202: 343-352. 9914143
Hewes, R. S. and Taghert, P. H. (2001). Neuropeptides and neuropeptide receptors in the Drosophila melanogaster genome. Genome Res. 11: 1126-1142. 11381038
Kim, Y. J., Zitnan, D., Galizia, C. G., Cho, K. H. and Adams, M. E. (2006a). A command chemical triggers an innate behavior by sequential activation of multiple peptidergic ensembles. Curr. Biol. 16: 1395-1407. 16860738
Kim, Y. J., Zitnan, D., Cho, K. H., Schooley, D. A., Mizoguchi, A. and Adams, M. E. (2006b). Central peptidergic ensembles associated with organization of an innate behavior. Proc. Natl. Acad. Sci. 103(38): 14211-6. 16968777
Kolhekar, A. S., Roberts, M. S., Jiang, N., Johnson, R. C., Mains, R. E., Eipper, B. A. and Taghert, P. H. (1997). Neuropeptide amidation in Drosophila: separate genes encode the two enzymes catalyzing amidation. J. Neurosci. 17: 1363-1376. 9006979
Lahr, E. C., Dean, D. and Ewer, J. (2012). Genetic analysis of ecdysis behavior in Drosophila reveals partially overlapping functions of two unrelated neuropeptides. J. Neurosci. 32(20): 6819-29. PubMed Citation: 22593051
Lehman, H. K., et al. (1993). Crustacean cardioactive peptide in the sphinx moth, Manduca sexta. Peptides 14(4): 735-41. 8234018
Loi, P. K., Emmal, S. A., Park, Y. and Tublitz, N. J. (2001). Indentification, sequence and expression of a crustacean cardioactive peptide (CCAP) gene in the moth Manduca sexta. J. Exp. Biol. 204,2803-2816. 11683436 .
McNabb, S. L., Baker, J. D., Agapite, J., Steller, H., Riddiford, L. M. and Truman, J. W. (1997). Disruption of behavioral sequence by targeted death of peptidergic neurons in Drosophila. Neuron 19: 813-823. 9354328
McNeil, G. P., Zhang, X., Genova, G. and Jackson, F. R. (1998). A molecular rhythm mediating circadian clock output in Drosophila. Neuron 20: 297-303. 9491990
Newby, L. M. and Jackson, F. R. (1993). A new biological rhythm mutant of Drosophila melanogaster that identifies a gene with an essential embryonic function. Genetics 135: 1077-1090. 8307324
Nichols, R., Kaminski, S., Walling, E. and Zornik, E. (1999). Regulating the activity of a cardioacceleratory peptide. Peptides 20, 1153-1158. 10573286
Park, J. H., Schroeder, A. J., Helfrich-Förster, C., Jackson, F. R. and Ewer, J. (2003). Targeted ablation of CCAP neuropeptide-containing neurons of Drosophila causes specific defects in execution and circadian timing of ecdysis behavior. Development 130: 2645-2656. 12736209
Park, Y., Filippov, V., Gill, S. S. and Adams, M. E. (2002a). Deletion of the ecdysis-triggering hormone gene leads to a lethal ecdysis deficiency. Development 129: 493-503. 11807040
Park, Y., Kim, Y. J. and Adams, M. E. (2002b). Identification of G protein-coupled receptors for Drosophila PRXamide peptides, CCAP, corazonin, and AKH supports a theory of ligand-receptor coevolution. Proc. Natl. Acad. Sci. 99: 11423-11428. 12177421
Phlippen, M. K., Webster, S. G., Chung, J. S. and Dircksen, H. (2000). Ecdysis of decapod crustaceans is associated with a dramatic release of crustacean cardioactive peptide into the haemolymph. J, Exp, Biol. 203: 521-536. 10637181
Stangier J, Hilbich C, Dircksen H, Keller R. (1988). Distribution of a novel cardioactive neuropeptide (CCAP) in the nervous system of the shore crab Carcinus maenas. Peptides 9(4): 795-800. 3226956
Veelaert, D., Passier, P., Devreese, B., Vanden Broeck, J., Van Beeumen, J., Vullings, H. G. B., Diederen, J. H. B., Schoofs, L. and De Loof, A. (1997). Endocrinology 138: 138-142. 8977396
Veverytsa, L. and Allan, D. W. (2011). Retrograde BMP signaling controls Drosophila behavior through regulation of a peptide hormone battery. Development 138(15): 3147-57. PubMed Citation: 21750027
Veverytsa, L. and Allan, D. W. (2012). Temporally tuned neuronal differentiation supports the functional remodeling of a neuronal network in Drosophila. Proc. Natl. Acad. Sci. 109(13): E748-56. PubMed Citation: 22393011
Zhang, X., McNeil, G. P., Hilderbrand-Chae, M. J., Franklin, T. M., Schroeder, A. J. and Jackson, F. R. (2000). Circadian regulation of the Lark RNA-binding protein within identifiable neurosecretory cells. J. Neurobiol. 45: 14-29. 10992253
Zitnan, D. and Adams, M. E. (2000). Excitatory and inhibitory roles of central ganglia in initiation of the insect ecdysis behavioural sequence. J. Exp. Biol. 203: 1329-1340. 10729281
date revised: 10 November 2012
Home page: The Interactive Fly © 2003 Thomas B. Brody, Ph.D.
The Interactive Fly resides on the
Society for Developmental Biology's Web server.