Development and Stem Cells Program, Monash Biomedicine Discovery Institute and Department of Anatomy and Developmental Biology, Monash University, Melbourne, Victoria, Australia.
Biotech Research and Innovation Centre, University of Copenhagen, Copenhagen, Denmark.
PLoS Genet. 2018 Sep 28;14(9):e1007670. doi: 10.1371/journal.pgen.1007670. eCollection 2018 Sep.
Rac GTPases act as master switches to coordinate multiple interweaved signaling pathways. A major function for Rac GTPases is to control neurite development by influencing downstream effector molecules and pathways. In Caenorhabditis elegans, the Rac proteins CED-10, RAC-2 and MIG-2 act in parallel to control axon outgrowth and guidance. Here, we have identified a single glycine residue in the CED-10/Rac1 Switch 1 region that confers a non-redundant function in axon outgrowth but not guidance. Mutation of this glycine to glutamic acid (G30E) reduces GTP binding and inhibits axon outgrowth but does not affect other canonical CED-10 functions. This demonstrates previously unappreciated domain-specific functions within the CED-10 protein. Further, we reveal that when CED-10 function is diminished, the adaptor protein NAB-1 (Neurabin) and its interacting partner SYD-1 (Rho-GAP-like protein) can act as inhibitors of axon outgrowth. Together, we reveal that specific domains and residues within Rac GTPases can confer context-dependent functions during animal development.
Rac GTPases 充当协调多个交织信号通路的主开关。Rac GTPases 的主要功能之一是通过影响下游效应分子和途径来控制神经突发育。在秀丽隐杆线虫中,Rac 蛋白 CED-10、RAC-2 和 MIG-2 平行作用以控制轴突生长和导向。在这里,我们在 CED-10/Rac1 Switch 1 区域中鉴定了一个单一的甘氨酸残基,该残基赋予轴突生长而非导向的非冗余功能。将该甘氨酸突变为谷氨酸(G30E)会降低 GTP 结合并抑制轴突生长,但不会影响 CED-10 的其他典型功能。这证明了 CED-10 蛋白内以前未被重视的特定域功能。此外,我们揭示了当 CED-10 功能减弱时,接头蛋白 NAB-1(神经连接蛋白)及其相互作用伙伴 SYD-1(Rho-GAP 样蛋白)可以作为轴突生长的抑制剂。总之,我们揭示了 Rac GTPases 中的特定结构域和残基可以在动物发育过程中赋予上下文相关的功能。