EGFR and FGFR pathways have distinct roles in Drosophila mushroom body development and ethanol-induced behavior

Epidermal Growth Factor Receptor (EGFR) signaling has a conserved role in ethanol-induced behavior in flies and mice, affecting ethanol-induced sedation in both species. However it is not known what other effects EGFR signaling may have on ethanol-induced behavior, or what roles other Receptor Tyros...

Full description

Saved in:
Bibliographic Details
Published in:PloS one Vol. 9; no. 1; p. e87714
Main Authors: King, Ian F G, Eddison, Mark, Kaun, Karla R, Heberlein, Ulrike
Format: Journal Article
Language:English
Published: United States Public Library of Science 31-01-2014
Public Library of Science (PLoS)
Subjects:
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:Epidermal Growth Factor Receptor (EGFR) signaling has a conserved role in ethanol-induced behavior in flies and mice, affecting ethanol-induced sedation in both species. However it is not known what other effects EGFR signaling may have on ethanol-induced behavior, or what roles other Receptor Tyrosine Kinase (RTK) pathways may play in ethanol induced behaviors. We examined the effects of both the EGFR and Fibroblast Growth Factor Receptor (FGFR) RTK signaling pathways on ethanol-induced enhancement of locomotion, a behavior distinct from sedation that may be associated with the rewarding effects of ethanol. We find that both EGFR and FGFR genes influence ethanol-induced locomotion, though their effects are opposite - EGFR signaling suppresses this behavior, while FGFR signaling promotes it. EGFR signaling affects development of the Drosophila mushroom bodies in conjunction with the JNK MAP kinase basket (bsk), and with the Ste20 kinase tao, and we hypothesize that the EGFR pathway affects ethanol-induced locomotion through its effects on neuronal development. We find, however, that FGFR signaling most likely affects ethanol-induced behavior through a different mechanism, possibly through acute action in adult neurons.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
Competing Interests: The authors have declared that no competing interests exist.
Current address: Howard Hughes Medical Institute, Janelia Farm Research Campus, Ashburn, Virginia, United States of America
Conceived and designed the experiments: IFGK UH. Performed the experiments: IFGK ME KRK. Wrote the paper: IFGK.
Current address: Department of Cell Biology and Physiology, University of North Carolina, Chapel Hill, North Carolina, United States of America
Current address: Department of Neuroscience, Brown University, Providence, Rhode Island, United States of America
ISSN:1932-6203
1932-6203
DOI:10.1371/journal.pone.0087714