TY - JOUR
T1 - A conserved GEF for Rho-family GTPases acts in an EGF signaling pathway to promote sleep-like quiescence in Caenorhabditis elegans
AU - Fry, Amanda L.
AU - Laboy, Jocelyn T.
AU - Huang, Huiyan
AU - Hart, Anne C.
AU - Norman, Kenneth R.
N1 - Funding Information:
We thank the people in the Norman laboratory for help with cloning and transgenesis and valuable discussions. Many strains were provided by the Caenorhabditis Genetics Center, which is funded by the National Institutes of Health (NIH) Office of Research Infrastructure Programs (P40-OD010440). This work was supported by NIH grants GM-088213 (K.N.) and NS-055813 (A.H.), as well as a Brown Institute for Brain Science and the Norman Prince Neuro-sciences Institute Postdoctoral Fellowship in Translational Neuroscience (H.H.).
Publisher Copyright:
© 2016 by the Genetics Society of America.
PY - 2016/3
Y1 - 2016/3
N2 - Sleep is evolutionarily conserved and required for organism homeostasis and survival. Despite this importance, the molecular and cellular mechanisms underlying sleep are not well understood. Caenorhabditis elegans exhibits sleep-like behavioral quiescence and thus provides a valuable, simple model system for the study of cellular and molecular regulators of this process. In C. elegans, epidermal growth factor receptor (EGFR) signaling is required in the neurosecretory neuron ALA to promote sleep-like behavioral quiescence after cellular stress. We describe a novel role for VAV-1, a conserved guanine nucleotide exchange factor (GEF) for Rho-family GTPases, in regulation of sleep-like behavioral quiescence. VAV-1, in a GEF-dependent manner, acts in ALA to suppress locomotion and feeding during sleep-like behavioral quiescence in response to cellular stress. Additionally, VAV-1 activity is required for EGF-induced sleep-like quiescence and normal levels of EGFR and secretory dense core vesicles in ALA. Importantly, the role of VAV-1 in promoting cellular stress–induced behavioral quiescence is vital for organism health because VAV-1 is required for normal survival after cellular stress.
AB - Sleep is evolutionarily conserved and required for organism homeostasis and survival. Despite this importance, the molecular and cellular mechanisms underlying sleep are not well understood. Caenorhabditis elegans exhibits sleep-like behavioral quiescence and thus provides a valuable, simple model system for the study of cellular and molecular regulators of this process. In C. elegans, epidermal growth factor receptor (EGFR) signaling is required in the neurosecretory neuron ALA to promote sleep-like behavioral quiescence after cellular stress. We describe a novel role for VAV-1, a conserved guanine nucleotide exchange factor (GEF) for Rho-family GTPases, in regulation of sleep-like behavioral quiescence. VAV-1, in a GEF-dependent manner, acts in ALA to suppress locomotion and feeding during sleep-like behavioral quiescence in response to cellular stress. Additionally, VAV-1 activity is required for EGF-induced sleep-like quiescence and normal levels of EGFR and secretory dense core vesicles in ALA. Importantly, the role of VAV-1 in promoting cellular stress–induced behavioral quiescence is vital for organism health because VAV-1 is required for normal survival after cellular stress.
KW - Behavioral quiescence
KW - Caenorhabditis elegans
KW - Sleep
KW - Vav
UR - http://www.scopus.com/inward/record.url?scp=84979944470&partnerID=8YFLogxK
U2 - 10.1534/genetics.115.183038
DO - 10.1534/genetics.115.183038
M3 - Article
C2 - 26801183
AN - SCOPUS:84979944470
SN - 0016-6731
VL - 202
SP - 1153
EP - 1166
JO - Genetics
JF - Genetics
IS - 3
ER -