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R-Ras填补了信号素信号传导中的另一个GAP。

R-Ras fills another GAP in semaphorin signalling.

作者信息

Pasterkamp R Jeroen

机构信息

Department of Pharmacology and Anatomy, Rudolf Magnus Institute of Neuroscience, University Medical Center Utrecht, Universiteitsweg 100, 3584 CG Utrecht, The Netherlands.

出版信息

Trends Cell Biol. 2005 Feb;15(2):61-4. doi: 10.1016/j.tcb.2004.12.005.

Abstract

Plexins are cell-surface receptors for the semaphorin family of neuronal guidance cues. Following semaphorin binding, the plexin cytoplasmic region initiates poorly understood signal-transduction events that lead to modifications of the cytoskeleton. Recent findings shed new light on the signalling network downstream of semaphorins and plexins by demonstrating that one of the plexins, plexin-B1, possesses an intrinsic GTPase-activating protein (GAP) activity towards R-Ras. Inactivation of R-Ras by the plexin-B1 GAP domains is required for plexin-B1-mediated effects on the cytoskeleton. These results indicate that plexins not only bind to but also regulate directly the activity of some of their downstream effectors.

摘要

丛状蛋白是神经导向信号分子semaphorin家族的细胞表面受体。在semaphorin结合后,丛状蛋白的胞质区域启动了人们了解甚少的信号转导事件,这些事件导致细胞骨架的改变。最近的研究结果通过证明丛状蛋白之一丛状蛋白-B1对R-Ras具有内在的GTP酶激活蛋白(GAP)活性,为semaphorin和丛状蛋白下游的信号网络提供了新的线索。丛状蛋白-B1的GAP结构域使R-Ras失活是丛状蛋白-B1介导的对细胞骨架作用所必需的。这些结果表明,丛状蛋白不仅与其一些下游效应器结合,而且还直接调节它们的活性。

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