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小GTP酶Rac1在痘苗病毒基于肌动蛋白的运动中所起的作用。

A role for the small GTPase Rac1 in vaccinia actin-based motility.

作者信息

Alvarez Diego E, Agaisse Hervé

机构信息

a Instituto de Investigaciones Biotecnológicas Dr. Rodolfo A. Ugalde ; Universidad Nacional de San Martín-CONICET ; San Martín , Buenos Aires , Argentina.

出版信息

Small GTPases. 2014;5(2):e29038. doi: 10.4161/sgtp.29038. Epub 2014 Oct 31.

Abstract

Vaccinia virus dissemination relies on the recruitment of the nucleation promoting factor N-WASP underneath cell-associated extracellular virus (CEVs) and subsequent recruitment and activation of the ARP2/3 complex, a major actin nucleator of the host cell. We have recently discovered that, in addition to the N-WASP/ARP2/3 pathway, vaccinia actin-based motility also relies on the small GTPase Rac1 and its downstream effector the formin-type actin nucleator FHOD1. Here we discuss the potential signaling mechanisms supporting the integration of the N-WASP/ARP2/3 and Rac1/FHOD1 pathways. We suggest the existence of a receptor tyrosine kinase family member that would integrate the Src-dependent activation of the N-WASP/ARP2/3 pathway and the GTP exchange factor-dependent activation of the Rac1/FHOD1 pathway.

摘要

痘苗病毒的传播依赖于在细胞相关细胞外病毒(CEV)下方募集成核促进因子N-WASP,以及随后募集和激活ARP2/3复合物,后者是宿主细胞主要的肌动蛋白成核因子。我们最近发现,除了N-WASP/ARP2/3途径外,基于肌动蛋白的痘苗病毒运动还依赖于小GTP酶Rac1及其下游效应器formin型肌动蛋白成核因子FHOD1。在这里,我们讨论支持N-WASP/ARP2/3和Rac1/FHOD1途径整合的潜在信号机制。我们认为存在一种受体酪氨酸激酶家族成员,它将整合N-WASP/ARP2/3途径的Src依赖性激活和Rac1/FHOD1途径的GTP交换因子依赖性激活。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/306f/4205144/84d4795702fd/sgtp-5-e29038-g1.jpg

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