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用于细胞极性的蛋白质聚类:以Par-3为例

Protein clustering for cell polarity: Par-3 as a paradigm.

作者信息

Harris Tony J C

机构信息

Department of Cell & Systems Biology, University of Toronto, Toronto, Canada.

出版信息

F1000Res. 2017 Aug 31;6:1620. doi: 10.12688/f1000research.11976.1. eCollection 2017.

DOI:10.12688/f1000research.11976.1
PMID:29026528
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5583741/
Abstract

The scaffold protein Par-3 ( Bazooka) is a central organizer of cell polarity across animals. This review focuses on how the clustering of Par-3 contributes to cell polarity. It begins with the Par-3 homo-oligomerization mechanism and its regulation by Par-1 phosphorylation. The role of polarized cytoskeletal networks in distributing Par-3 clusters to one end of the cell is then discussed, as is the subsequent maintenance of polarized Par-3 clusters through hindered mobility and inhibition from the opposite pole. Finally, specific roles of Par-3 clusters are reviewed, including the bundling of microtubules, the cortical docking of centrosomes, the growth and positioning of cadherin-catenin clusters, and the inhibition of the Par-6-aPKC kinase cassette. Examples are drawn from , mammalian cell culture, and biochemical studies.

摘要

支架蛋白Par-3(巴左卡)是动物细胞极性的核心组织者。本综述重点关注Par-3的聚集如何促成细胞极性。它始于Par-3的同型寡聚化机制及其受Par-1磷酸化的调控。接着讨论了极化细胞骨架网络在将Par-3簇分布到细胞一端中的作用,以及随后通过受阻迁移和来自相反极的抑制来维持极化的Par-3簇。最后,综述了Par-3簇的特定作用,包括微管的捆绑、中心体的皮质对接、钙黏蛋白-连环蛋白簇的生长和定位,以及对Par-6-aPKC激酶盒的抑制。实例取自、哺乳动物细胞培养和生化研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce0c/5583741/94db71626f17/f1000research-6-12949-g0000.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce0c/5583741/94db71626f17/f1000research-6-12949-g0000.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce0c/5583741/94db71626f17/f1000research-6-12949-g0000.jpg

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Dev Cell. 2017 Aug 21;42(4):416-434.e11. doi: 10.1016/j.devcel.2017.07.024.
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aPKC Cycles between Functionally Distinct PAR Protein Assemblies to Drive Cell Polarity.非典型蛋白激酶C在功能不同的PAR蛋白组装体之间循环以驱动细胞极性。
Dev Cell. 2017 Aug 21;42(4):400-415.e9. doi: 10.1016/j.devcel.2017.07.007. Epub 2017 Aug 3.
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Cortical forces and CDC-42 control clustering of PAR proteins for Caenorhabditis elegans embryonic polarization.
Thy-1(CD90)调控间充质细胞的细胞黏附与迁移:对黏附体、机械力和信号通路的见解
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Persistent cell contacts enable E-cadherin/HMR-1- and PAR-3-based symmetry breaking within a developing C. elegans epithelium.持续的细胞接触使得 E-钙黏蛋白/HMR-1-和 PAR-3 能够在一个正在发育的 C.elegans 上皮细胞中打破对称性。
Dev Cell. 2023 Oct 9;58(19):1830-1846.e12. doi: 10.1016/j.devcel.2023.07.008. Epub 2023 Aug 7.
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