Gene Expression Laboratory and the Howard Hughes Medical Institute, Salk Institute for Biological Studies, 10010 North Torrey Pines, La Jolla, CA 92037, USA; San Raffaele Scientific Institute, Division of Neuroscience, via Olgettina 60, 20132 Milan, Italy.
San Raffaele Scientific Institute, Division of Neuroscience, via Olgettina 60, 20132 Milan, Italy.
Neuron. 2019 May 8;102(3):602-620.e9. doi: 10.1016/j.neuron.2019.02.034. Epub 2019 Mar 19.
The rich functional diversity of the nervous system is founded in the specific connectivity of the underlying neural circuitry. Neurons are often preprogrammed to respond to multiple axon guidance signals because they use sequential guideposts along their pathways, but this necessitates a strict spatiotemporal regulation of intracellular signaling to ensure the cues are detected in the correct order. We performed a mouse mutagenesis screen and identified the Rho GTPase antagonist p190RhoGAP as a critical regulator of motor axon guidance. Rather than acting as a compulsory signal relay, p190RhoGAP uses a non-conventional GAP-independent mode to transiently suppress attraction to Netrin-1 while motor axons exit the spinal cord. Once in the periphery, a subset of axons requires p190RhoGAP-mediated inhibition of Rho signaling to target specific muscles. Thus, the multifunctional activity of p190RhoGAP emerges from its modular design. Our findings reveal a cell-intrinsic gate that filters conflicting signals, establishing temporal windows of signal detection.
神经系统丰富的功能多样性源于其基础神经网络的特定连接性。神经元通常被预先编程为对多种轴突导向信号做出反应,因为它们在路径上使用顺序引导物,但这需要严格的细胞内信号转导时空调节,以确保线索按正确的顺序被检测到。我们进行了一次小鼠诱变筛选,并鉴定出 Rho GTPase 拮抗剂 p190RhoGAP 是运动轴突导向的关键调节因子。p190RhoGAP 并没有作为必需的信号中继,而是采用非传统的 GAP 非依赖性模式,短暂抑制对 Netrin-1 的吸引力,而运动轴突离开脊髓。一旦进入外周,一部分轴突需要 p190RhoGAP 介导的 Rho 信号抑制来靶向特定的肌肉。因此,p190RhoGAP 的多功能活性源自其模块化设计。我们的发现揭示了一个内在的细胞门,它可以过滤冲突的信号,建立信号检测的时间窗口。