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First published online January 27, 2004
Journal of Experimental Biology 207, 743-748 (2004)
Published by The Company of Biologists 2004
doi: 10.1242/jeb.00818
Drosophila CG8422 encodes a functional diuretic hormone receptor

1 Department of Anatomy and Neurobiology, Washington University School of
Medicine, Saint Louis, MO 63110, USA
2 Department of Cell Biology, Duke University, Durham, NC 27710,
USA
Author for correspondence (e-mail:
taghertp{at}pcg.wustl.edu)
Accepted 3 December 2003
Diuretic hormone 44 (DH) is a bioactive neuropeptide that mediates osmotic
balance in a wide variety of insects through increases in cAMP. It is
structurally similar to mammalian corticotrophin releasing factor (CRF)
peptides. In the moth Manduca and the cricket Acheta,
functional studies have shown that its cognate receptor (DH-R) is related to
the mammalian CRF receptor. The Drosophila genome contains two genes
(CG8422 and CG12370) orthologous to Manduca and
Acheta DH-Rs. Here, we present multiple lines of evidence to support
the hypothesis that the orphan CG8422 G-protein-coupled receptor is a
functional DH-R. When expressed in mammalian cells, CG8422 conferred
selective sensitivity to DH, as indicated by translocation of a
ß-arrestin-2-GFP reporter from the cytoplasm to the cell membrane.
Consistent with its in vivo activities in other insects, DH
activation of CG8422 elicited increases in a cAMP reporter system
(CRE-luciferase), with an EC50 of 1.7 nmol l-1.
CG8422 activation by DH also led to increases in intracellular
calcium but at substantially higher doses (EC50
300 nmol
l-1). By microarray analysis, the CG8422 transcript was
detectable in Drosophila head mRNA of different genotypes and under
different environmental conditions. The identification of a
Drosophila receptor for the DH neuropeptide provides a basis for
genetic analysis of this critical factor's roles in maintaining physiological
homeostasis.
Key words: neuropeptide, GPCR, receptor, Drosophila, diuretic hormone, ß-arrestin-2, GFP, cAMP
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