Department of Biology, University of Miami, Coral Gables, FL 33146, USA.
Genetics. 2022 Jul 4;221(3). doi: 10.1093/genetics/iyac084.
Activated Gαq signals through phospholipase-Cβ and Trio, a Rho GTPase exchange factor (RhoGEF), but how these distinct effector pathways promote cellular responses to neurotransmitters like serotonin remains poorly understood. We used the egg-laying behavior circuit of Caenorhabditis elegans to determine whether phospholipase-Cβ and Trio mediate serotonin and Gαq signaling through independent or related biochemical pathways. Our genetic rescue experiments suggest that phospholipase-Cβ functions in neurons while Trio Rho GTPase exchange factor functions in both neurons and the postsynaptic vulval muscles. While Gαq, phospholipase-Cβ, and Trio Rho GTPase exchange factor mutants fail to lay eggs in response to serotonin, optogenetic stimulation of the serotonin-releasing HSN neurons restores egg laying only in phospholipase-Cβ mutants. Phospholipase-Cβ mutants showed vulval muscle Ca2+ transients while strong Gαq and Trio Rho GTPase exchange factor mutants had little or no vulval muscle Ca2+ activity. Treatment with phorbol 12-myristate 13-acetate that mimics 1,2-diacylglycerol, a product of PIP2 hydrolysis, rescued egg-laying circuit activity and behavior defects of Gαq signaling mutants, suggesting both phospholipase-C and Rho signaling promote synaptic transmission and egg laying via modulation of 1,2-diacylglycerol levels. 1,2-Diacylglycerol activates effectors including UNC-13; however, we find that phorbol esters, but not serotonin, stimulate egg laying in unc-13 and phospholipase-Cβ mutants. These results support a model where serotonin signaling through Gαq, phospholipase-Cβ, and UNC-13 promotes neurotransmitter release, and that serotonin also signals through Gαq, Trio Rho GTPase exchange factor, and an unidentified, phorbol 12-myristate 13-acetate-responsive effector to promote postsynaptic muscle excitability. Thus, the same neuromodulator serotonin can signal in distinct cells and effector pathways to coordinate activation of a motor behavior circuit.
激活的 Gαq 通过磷脂酶-Cβ 和 Trio(一种 Rho GTP 酶交换因子(RhoGEF))发出信号,但这些不同的效应物途径如何促进细胞对血清素等神经递质的反应仍知之甚少。我们使用秀丽隐杆线虫的产卵行为回路来确定磷脂酶-Cβ 和 Trio 是否通过独立或相关的生化途径介导血清素和 Gαq 信号。我们的遗传挽救实验表明,磷脂酶-Cβ 在神经元中起作用,而 Trio Rho GTP 酶交换因子在神经元和突触后 vulval 肌肉中都起作用。虽然 Gαq、磷脂酶-Cβ 和 Trio Rho GTP 酶交换因子突变体不能对血清素作出产卵反应,但光遗传学刺激释放血清素的 HSN 神经元只能恢复磷脂酶-Cβ 突变体的产卵。磷脂酶-Cβ 突变体显示 vulval 肌肉 Ca2+瞬变,而强 Gαq 和 Trio Rho GTP 酶交换因子突变体几乎没有或没有 vulval 肌肉 Ca2+活性。用佛波醇 12-肉豆蔻酸 13-乙酸酯处理,模拟 PIP2 水解的产物 1,2-二酰基甘油,挽救了 Gαq 信号突变体的产卵电路活性和行为缺陷,表明磷脂酶-C 和 Rho 信号都通过调节 1,2-二酰基甘油水平来促进突触传递和产卵。1,2-二酰基甘油激活包括 UNC-13 在内的效应物;然而,我们发现佛波醇酯,但不是血清素,刺激 unc-13 和磷脂酶-Cβ 突变体产卵。这些结果支持了一种模型,即 Gαq、磷脂酶-Cβ 和 UNC-13 通过血清素信号促进神经递质释放,而血清素也通过 Gαq、Trio Rho GTP 酶交换因子和一种未鉴定的、佛波醇 12-肉豆蔻酸 13-乙酸酯反应性效应物信号来促进突触后肌肉兴奋性。因此,相同的神经调质血清素可以在不同的细胞和效应物途径中发出信号,以协调运动行为回路的激活。