Hoyt Jill M, Wilson Samuel K, Kasa Madhuri, Rise Jeremy S, Topalidou Irini, Ailion Michael
Department of Biochemistry, University of Washington, Seattle, Washington 98195.
Department of Biochemistry, University of Washington, Seattle, Washington 98195
G3 (Bethesda). 2017 Sep 7;7(9):2979-2989. doi: 10.1534/g3.117.043273.
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 for suppressors of activated Gq. One of the suppressors is an allele of , which encodes a mitogen-activated protein kinase kinase (MAPKK) in the p38 MAPK pathway. Here, we show that mutants have a slow locomotion rate and that acts in acetylcholine neurons to modulate both locomotion rate and Gq signaling. Furthermore, we find that 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).
Gq是一种异源三聚体G蛋白,在神经元中广泛表达并调节神经元活动。为了确定调节神经元Gq信号传导的途径,我们对激活的Gq的抑制因子进行了正向遗传学筛选。其中一个抑制因子是一个等位基因,它在p38丝裂原活化蛋白激酶(MAPK)途径中编码一种丝裂原活化蛋白激酶激酶(MAPKK)。在这里,我们表明该突变体具有缓慢的运动速率,并且该基因在乙酰胆碱能神经元中发挥作用,以调节运动速率和Gq信号传导。此外,我们发现该基因在成熟神经元中发挥作用以调节运动。使用遗传学和行为学方法,我们证明p38 MAPK途径的其他成分在调节运动和Gq信号传导中也发挥积极作用。最后,我们发现SEK-1 p38 MAPK途径中的突变体部分抑制了钠泄漏通道NCA-1/NALCN(Gq信号传导的下游靶点)的激活突变体。我们的结果表明,SEK-1 p38途径可能通过NCA-1(unc-77)调节Gq信号传导的输出。