Schumacher Stefan, Franke Kristin
Institute of Molecular and Cellular Anatomy, Ulm University, Ulm, Germany.
Small GTPases. 2013 Jan-Mar;4(1):42-6. doi: 10.4161/sgtp.22922. Epub 2013 Jan 1.
RhoG is a member of the Rho family of small GTPases sharing highest sequence similarity with Rac and Cdc42. Mig-2 and Mtl represent the functional equivalents of RhoG in Caenorhabditis elegans and Drosophila, respectively. RhoG has attracted great interest because it plays a central role in the regulation of cytoskeletal reorganization in various physiological and pathophysiological situations. For example, it is fundamental to phagocytotic processes, is able to regulate gene expression, cell survival and proliferation, and is involved in cell migration and in the invasion of pathogenic bacteria. The activation of Rac1 via an ELMO/Dock180 module has been elaborated to be important for RhoG signaling. Although a stimulatory role for neurite outgrowth in the pheochromocytoma PC12 cell line has been assigned to RhoG, the exact function of this GTPase for the development of the processes of primary neurons remains to be clarified. In this view, we discuss the impact of RhoG on axonal and dendritic differentiation, its role as a conductor of Rac1 and Cdc42 activity and the functional regulation of RhoG expression by the microRNA miR-124.
RhoG是小GTP酶Rho家族的成员,与Rac和Cdc42具有最高的序列相似性。Mig-2和Mtl分别代表秀丽隐杆线虫和果蝇中RhoG的功能等效物。RhoG引起了极大的兴趣,因为它在各种生理和病理生理情况下的细胞骨架重组调节中起着核心作用。例如,它对吞噬过程至关重要,能够调节基因表达、细胞存活和增殖,并参与细胞迁移和病原菌的入侵。通过ELMO/Dock180模块激活Rac1已被阐述为对RhoG信号传导很重要。尽管已将RhoG对嗜铬细胞瘤PC12细胞系中神经突生长的刺激作用归因于RhoG,但这种GTP酶对原代神经元突起发育的确切功能仍有待阐明。鉴于此,我们讨论了RhoG对轴突和树突分化的影响、其作为Rac1和Cdc42活性传导者的作用以及微小RNA miR-124对RhoG表达的功能调节。