肌动蛋白单体结合蛋白对细胞骨架动力学的调控

Regulation of cytoskeletal dynamics by actin-monomer-binding proteins.

作者信息

Paavilainen Ville O, Bertling Enni, Falck Sandra, Lappalainen Pekka

机构信息

Program in Cellular Biotechnology, Institute of Biotechnology, PO Box 56, University of Helsinki, Helsinki 00014, Finland.

出版信息

Trends Cell Biol. 2004 Jul;14(7):386-94. doi: 10.1016/j.tcb.2004.05.002.

Abstract

The actin cytoskeleton is a vital component of several key cellular and developmental processes in eukaryotes. Many proteins that interact with filamentous and/or monomeric actin regulate the structure and dynamics of the actin cytoskeleton. Actin-filament-binding proteins control the nucleation, assembly, disassembly and crosslinking of actin filaments, whereas actin-monomer-binding proteins regulate the size, localization and dynamics of the large pool of unpolymerized actin in cells. In this article, we focus on recent advances in understanding how the six evolutionarily conserved actin-monomer-binding proteins - profilin, ADF/cofilin, twinfilin, Srv2/CAP, WASP/WAVE and verprolin/WIP - interact with actin monomers and regulate their incorporation into filament ends. We also present a model of how, together, these ubiquitous actin-monomer-binding proteins contribute to cytoskeletal dynamics and actin-dependent cellular processes.

摘要

肌动蛋白细胞骨架是真核生物中几个关键细胞和发育过程的重要组成部分。许多与丝状和/或单体肌动蛋白相互作用的蛋白质调节着肌动蛋白细胞骨架的结构和动力学。肌动蛋白丝结合蛋白控制肌动蛋白丝的成核、组装、解聚和交联,而肌动蛋白单体结合蛋白则调节细胞中大量未聚合肌动蛋白的大小、定位和动力学。在本文中,我们重点关注在理解六种进化上保守的肌动蛋白单体结合蛋白——丝切蛋白、ADF/丝切蛋白、双丝蛋白、Srv2/CAP、WASP/WAVE和维普洛林/WIP——如何与肌动蛋白单体相互作用并调节它们掺入丝末端方面的最新进展。我们还提出了一个模型,说明这些普遍存在的肌动蛋白单体结合蛋白如何共同促进细胞骨架动力学和肌动蛋白依赖性细胞过程。

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