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连接蛋白 43 C 末端:众说纷纭的尾巴。

The connexin 43 C-terminus: A tail of many tales.

机构信息

Department of Molecular Oncology, Institute for Cancer Research, University of Oslo, NO-0424 Oslo, Norway; Centre for Cancer Biomedicine, Faculty of Medicine, University of Oslo, NO-0424 Oslo, Norway.

STIM Laboratory ERL 7368 CNRS - Faculté des Sciences Fondamentales et Appliquées, Université de Poitiers, Poitiers 86073, France.

出版信息

Biochim Biophys Acta Biomembr. 2018 Jan;1860(1):48-64. doi: 10.1016/j.bbamem.2017.05.008. Epub 2017 May 16.

Abstract

Connexins are chordate gap junction channel proteins that, by enabling direct communication between the cytosols of adjacent cells, create a unique cell signalling network. Gap junctional intercellular communication (GJIC) has important roles in controlling cell growth and differentiation and in tissue development and homeostasis. Moreover, several non-canonical connexin functions unrelated to GJIC have been discovered. Of the 21 members of the human connexin family, connexin 43 (Cx43) is the most widely expressed and studied. The long cytosolic C-terminus (CT) of Cx43 is subject to extensive post-translational modifications that modulate its intracellular trafficking and gap junction channel gating. Moreover, the Cx43 CT contains multiple domains involved in protein interactions that permit crosstalk between Cx43 and cytoskeletal and regulatory proteins. These domains endow Cx43 with the capacity to affect cell growth and differentiation independently of GJIC. Here, we review the current understanding of the regulation and unique functions of the Cx43 CT, both as an essential component of full-length Cx43 and as an independent signalling hub. We highlight the complex regulatory and signalling networks controlled by the Cx43 CT, including the extensive protein interactome that underlies both gap junction channel-dependent and -independent functions. We discuss these data in relation to the recent discovery of the direct translation of specific truncated forms of Cx43. This article is part of a Special Issue entitled: Gap Junction Proteins edited by Jean Claude Herve.

摘要

连接蛋白是脊索动物间隙连接通道蛋白,通过使相邻细胞的细胞质直接通讯,形成独特的细胞信号网络。间隙连接细胞间通讯(GJIC)在控制细胞生长和分化以及组织发育和稳态中具有重要作用。此外,还发现了几种与 GJIC 无关的非典型连接蛋白功能。在人类连接蛋白家族的 21 个成员中,连接蛋白 43(Cx43)是表达最广泛和研究最多的。Cx43 的长细胞质 C 末端(CT)受到广泛的翻译后修饰的调节,这些修饰调节其细胞内运输和间隙连接通道门控。此外,Cx43 CT 包含多个参与蛋白相互作用的结构域,允许 Cx43 与细胞骨架和调节蛋白之间进行串扰。这些结构域使 Cx43 具有独立于 GJIC 影响细胞生长和分化的能力。在这里,我们综述了 Cx43 CT 的调节和独特功能的最新认识,既作为全长 Cx43 的重要组成部分,又作为独立的信号枢纽。我们强调了由 Cx43 CT 控制的复杂调节和信号网络,包括基础的间隙连接通道依赖和独立功能的广泛蛋白相互作用组。我们讨论了这些数据与最近发现的特定截断形式的 Cx43 的直接翻译的关系。本文是由 Jean Claude Herve 编辑的特刊“间隙连接蛋白”的一部分。

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