The SEK-1 p38 MAP Kinase Pathway Modulates Gq Signaling in Caenorhabditis elegans
Author(s) -
Jill M. Hoyt,
Samuel K. Wilson,
Madhuri Kasa,
Jeremy S. Rise,
Irini Topalidou,
Michael Ailion
Publication year - 2017
Publication title -
g3 genes genomes genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.468
H-Index - 66
ISSN - 2160-1836
DOI - 10.1534/g3.117.043273
Subject(s) - caenorhabditis elegans , gq alpha subunit , heterotrimeric g protein , microbiology and biotechnology , mapk/erk pathway , signal transduction , protein kinase a , biology , mutant , mitogen activated protein kinase , p38 mitogen activated protein kinases , g protein , kinase , genetics , gene
Gq is a heterotrimeric G protein that is widely expressed in neurons and regulates neuronal activity. To identify pathways regulating neuronal Gq signaling, we performed a forward genetic screen in Caenorhabditis elegans for suppressors of activated Gq. One of the suppressors is an allele of sek-1 , which encodes a mitogen-activated protein kinase kinase (MAPKK) in the p38 MAPK pathway. Here, we show that sek-1 mutants have a slow locomotion rate and that sek-1 acts in acetylcholine neurons to modulate both locomotion rate and Gq signaling. Furthermore, we find that sek-1 acts in mature neurons to modulate locomotion. Using genetic and behavioral approaches, we demonstrate that other components of the p38 MAPK pathway also play a positive role in modulating locomotion and Gq signaling. Finally, we find that mutants in the SEK-1 p38 MAPK pathway partially suppress an activated mutant of the sodium leak channel, NCA-1/NALCN, a downstream target of Gq signaling. Our results suggest that the SEK-1 p38 pathway may modulate the output of Gq signaling through NCA-1(unc-77).
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