Lamb Reagan, Scales Michael, Watkins Julie, Werner Martin, Cherra Salvatore J
Department of Neuroscience, University of Kentucky College of Medicine.
present address: Department of Genetics, Yale University School of Medicine.
bioRxiv. 2025 May 30:2025.05.27.656318. doi: 10.1101/2025.05.27.656318.
Small G proteins coordinate the development of nerve terminals. The activity of G proteins is finely tuned by GTPase regulatory proteins. Previously, we observed that PXF-1, a GTPase regulatory protein, is required for the function of cholinergic motor neurons. Here, we investigated how PXF-1 coordinates the development of presynaptic terminals at the molecular level. We observed that PXF-1 acts through RAP-1 to promote synapse development. Subsequently, we found that mutants display a reduction in RAC-2 activity, which is required for cholinergic synapse development. We observed that RAC-2 acts downstream of RAP-1. Finally, we identified a physical interaction between RAP-1 and TIAM-1, a Rac guanine exchange factor, which links PXF-1 function to the presynaptic actin cytoskeleton through RAC-2 activation. These findings highlight how small G protein signaling pathways interact to coordinate the development of presynaptic terminals.
小G蛋白协调神经末梢的发育。G蛋白的活性由GTP酶调节蛋白精细调控。此前,我们观察到PXF-1(一种GTP酶调节蛋白)是胆碱能运动神经元功能所必需的。在此,我们研究了PXF-1在分子水平上如何协调突触前末梢的发育。我们观察到PXF-1通过RAP-1发挥作用以促进突触发育。随后,我们发现突变体中RAC-2活性降低,而RAC-2活性是胆碱能突触发育所必需的。我们观察到RAC-2在RAP-1的下游发挥作用。最后,我们鉴定出RAP-1与Rac鸟嘌呤交换因子TIAM-1之间存在物理相互作用,该相互作用通过激活RAC-2将PXF-1的功能与突触前肌动蛋白细胞骨架联系起来。这些发现突出了小G蛋白信号通路如何相互作用以协调突触前末梢的发育。