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WASP 家族蛋白的细胞功能一览。

Cellular functions of WASP family proteins at a glance.

机构信息

Division of Oncology Research, College of Medicine, Mayo Clinic, Rochester, MN 55905, USA.

Department of Internal Medicine, UT Southwestern Medical Center, Dallas, TX 75390-9151, USA.

出版信息

J Cell Sci. 2017 Jul 15;130(14):2235-2241. doi: 10.1242/jcs.199570. Epub 2017 Jun 23.

DOI:10.1242/jcs.199570
PMID:28646090
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5536917/
Abstract

Proteins of the Wiskott-Aldrich syndrome protein (WASP) family function as nucleation-promoting factors for the ubiquitously expressed Arp2/3 complex, which drives the generation of branched actin filaments. Arp2/3-generated actin regulates diverse cellular processes, including the formation of lamellipodia and filopodia, endocytosis and/or phagocytosis at the plasma membrane, and the generation of cargo-laden vesicles from organelles including the Golgi, endoplasmic reticulum (ER) and the endo-lysosomal network. Recent studies have also identified roles for WASP family members in promoting actin dynamics at the centrosome, influencing nuclear shape and membrane remodeling events leading to the generation of autophagosomes. Interestingly, several WASP family members have also been observed in the nucleus where they directly influence gene expression by serving as molecular platforms for the assembly of epigenetic and transcriptional machinery. In this Cell Science at a Glance article and accompanying poster, we provide an update on the subcellular roles of WHAMM, JMY and WASH (also known as WASHC1), as well as their mechanisms of regulation and emerging functions within the cell.

摘要

Wiskott-Aldrich 综合征蛋白(WASP)家族的蛋白作为普遍表达的 Arp2/3 复合物的成核促进因子发挥作用,该复合物驱动分支肌动蛋白丝的生成。Arp2/3 生成的肌动蛋白调节多种细胞过程,包括质膜处的片状伪足和丝状伪足的形成、内吞作用和/或吞噬作用,以及来自高尔基体、内质网(ER)和内体-溶酶体网络等细胞器的载货物的小泡的生成。最近的研究还确定了 WASP 家族成员在促进中心体处的肌动蛋白动力学、影响核形状和膜重塑事件方面的作用,这些事件导致自噬体的生成。有趣的是,几个 WASP 家族成员也在核内被观察到,它们通过作为组装表观遗传和转录机制的分子平台,直接影响基因表达。在本期《细胞科学一览》文章和配套海报中,我们提供了 WHAMM、JMY 和 WASH(也称为 WASHC1)的亚细胞作用的最新信息,以及它们在细胞内的调节机制和新兴功能。

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2
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本文引用的文献

1
Defects in ER-endosome contacts impact lysosome function in hereditary spastic paraplegia.内质网-内体接触缺陷影响遗传性痉挛性截瘫中的溶酶体功能。
J Cell Biol. 2017 May 1;216(5):1337-1355. doi: 10.1083/jcb.201609033. Epub 2017 Apr 7.
2
Structural Insights of WHAMM's Interaction with Microtubules by Cryo-EM.通过冷冻电镜对WHAMM与微管相互作用的结构洞察
J Mol Biol. 2017 May 5;429(9):1352-1363. doi: 10.1016/j.jmb.2017.03.022. Epub 2017 Mar 25.
3
Drosophila WASH is required for integrin-mediated cell adhesion, cell motility and lysosomal neutralization.果蝇WASH蛋白对于整合素介导的细胞黏附、细胞运动及溶酶体中和作用是必需的。
J Cell Sci. 2017 Jan 15;130(2):344-359. doi: 10.1242/jcs.193086. Epub 2016 Nov 24.
4
WASH drives early recycling from macropinosomes and phagosomes to maintain surface phagocytic receptors.清洗驱动早期从巨胞饮体和吞噬体进行再循环,以维持表面吞噬受体。
Proc Natl Acad Sci U S A. 2016 Oct 4;113(40):E5906-E5915. doi: 10.1073/pnas.1524532113. Epub 2016 Sep 19.
5
Endosome-ER Contacts Control Actin Nucleation and Retromer Function through VAP-Dependent Regulation of PI4P.内体-内质网接触通过VAP依赖的PI4P调节控制肌动蛋白成核和回收体功能。
Cell. 2016 Jul 14;166(2):408-423. doi: 10.1016/j.cell.2016.06.037.
6
CCC- and WASH-mediated endosomal sorting of LDLR is required for normal clearance of circulating LDL.LDLR的CCCs和WASH介导的内体分选是循环LDL正常清除所必需的。
Nat Commun. 2016 Mar 11;7:10961. doi: 10.1038/ncomms10961.
7
Fat2 acts through the WAVE regulatory complex to drive collective cell migration during tissue rotation.Fat2通过WAVE调节复合体发挥作用,在组织旋转过程中驱动集体细胞迁移。
J Cell Biol. 2016 Feb 29;212(5):591-603. doi: 10.1083/jcb.201508081. Epub 2016 Feb 22.
8
Rab1 recruits WHAMM during membrane remodeling but limits actin nucleation.Rab1在膜重塑过程中招募WHAMM,但限制肌动蛋白成核。
Mol Biol Cell. 2016 Mar 15;27(6):967-78. doi: 10.1091/mbc.E15-07-0508. Epub 2016 Jan 28.
9
WHAMY is a novel actin polymerase promoting myoblast fusion, macrophage cell motility and sensory organ development in Drosophila.WHAMY是一种新型肌动蛋白聚合酶,可促进果蝇中的成肌细胞融合、巨噬细胞运动和感觉器官发育。
J Cell Sci. 2016 Feb 1;129(3):604-20. doi: 10.1242/jcs.179325. Epub 2015 Dec 16.
10
The centrosome is an actin-organizing centre.中心体是一个肌动蛋白组织中心。
Nat Cell Biol. 2016 Jan;18(1):65-75. doi: 10.1038/ncb3285. Epub 2015 Dec 14.