| The use 
              of Drosophila to study the control pathways for exogenous 
              and endogenous components of the ecdysis rhythm
               
              J. W. Truman, O. 
              Shafer & S. McNabb 
              Dept. of Zoology, 
              Univ. of Washington, Box 351800, Seattle, WA 98195-1800, USA The rhythm of adult 
              eclosion in Drosophila is one of the most extensively 
              studied rhythms in insects. The final form of the ecdysis rhythm, 
              however, is a product of endogenous time-keeping via the circadian 
              clock and responses to exogenous cues such as the lights-on 
              signal. The latter results in a pronounced skewing of the ecdysis 
              peak just following lights-on. Recent studies in both 
              Drosophila and the moth Manduca have shown that ecdysis 
              is controlled through a complex hormonal cascade that includes the 
              steroid hormone, 20 hydroxyecdysone (20E), and a series of peptide 
              hormones: eclosion hormone (EH), ecdysis-triggering hormone (ETH), 
              and crustacean cardioactive peptide (CCAP). We have been 
              interested in how endogenous and exogenous timing factors impinge 
              on this endocrine control pathway. Through a series of mutations 
              and genetically engineered flies, we have found that endogenous 
              and exogenous factors act through different portions of the 
              control cascade. Removal of the EH neurons renders the ecdysis 
              system incapable of responding to the lights-on signal. Although 
              we originally though that the lights-on signal acted to induce EH 
              release in Drosophila, we now have evidence that this 
              stimulus acts to shorten the delay between EH release and the 
              subsequent release of CCAP. In contrast to the lights-on response, 
              the circadian control of ecdysis in Drosophila does not require 
              the EH neurons. Nor does it apparently require ETH. We think that 
              there is a parallel pathway that can also activate the CCAP 
              neurons -- a prerequisite for ecdysis. This pathway likely 
              involves a circadian control over the timing of the 20E decline at 
              the end of metamorphosis. Evidence for this pathway will be 
              discussed. Index items:
              Drosophila melanogaster, circadian rhythms, photoreception
               
 
                
                Copyright: The copyrights of 
                this original work belong to the authors (see right-most box in 
                title table). This abstract appeared in Session 13 – INSECT 
                PHISIOLOGY, NEUROSCIENCES, IMMUNITY AND CELL BIOLOGY Symposium 
                and Poster Session, ABSTRACT BOOK II – XXI-International 
                Congress of Entomology, Brazil, August 20-26, 2000. 
                
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