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Wake Forest University

Genetic Dissection of DH31 Signaling in Drosophila

Abstract

dc:description.abstract

Dh31, which is homologous to the mammalian Calcitonin Gene-Related Peptide, is a multifunctional neuropeptide in Drosophila. To evaluate the roles of Dh31 signaling in Drosophila, we took advantage of the KG09001 line because it has a transposable element inserted in the third intron of the Dh31 gene. We employed an excision screen to mobilize the element and generated 500 excision lines. Evaluation of these excision lines led to the identification of a revertant, Dh31rev, and two mutant alleles, Dh3101 and Dh3102. Subsequent analysis of these alleles indicated that revertant lines exhibited wild type responses to osmotic and starvation stress, whereas mutant lines were hypersensitive to stress-inducing conditions. Expression analysis of Dh31 in both larval and adult CNS showed that mutant alleles had no DH31 immunoreactivity, while revertant lines appeared wild-type for Dh31 expression. Locomotor analysis of mutant lines demonstrated abnormal locomotor phenotypes under both normal and stress conditions. Provocatively, RNAi knockdown of the receptor for DH31, resulted in a phenocopy of lifespan phenotypes, but not locomotor phenotypes. Our results refine our understanding of the multiple roles of Dh31 signaling in Drosophila, and suggest a conservation of CGRP signaling in mediating stress behaviors throughout the Metazoa.

Degree

thesis:*
Grantor dc:publisher
Wake Forest University
Year dc:date.issued
2009

Author and committee

dc:creator, dc:contributor.*
Author dc:creator
  • Bretz, Colin

Subjects

dc:subject × 1

Rights

Language dc:language.iso
en_US

Identifiers

dc:identifier.*
Handle dc:identifier.uri
http://hdl.handle.net/10339/14900
OAI identifier oai:identifier
oai:wakespace.lib.wfu.edu:10339/14900

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Wake Forest University
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Last updated
2026-07-27
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citation

Bretz, Colin. Genetic Dissection of DH31 Signaling in Drosophila. Wake Forest University, 2009. http://hdl.handle.net/10339/14900