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细胞器间p53之旅的门票。

Tickets for p53 journey among organelles.

作者信息

Ferecatu Ioana, Rincheval Vincent, Mignotte Bernard, Vayssiere Jean-Luc

机构信息

Laboratoire de Genetique et Biologie Cellulaire, CNRS UMR 8159, Universite de Versailles Saint-Quentin-en-Yvelines, 45 avenue des Etats-Unis, 78035 Versailles cedex, France.

出版信息

Front Biosci (Landmark Ed). 2009 Jan 1;14(11):4214-28. doi: 10.2741/3524.

Abstract

A broad range of stressors - intrinsic and extrinsic to the cell - stabilize and activate p53, affecting it by a series of post-translational modifications such as phosphorylation, acetylation, ubiquitination, methylation and sumoylation. p53 is able to integrate each kind of post-translational modification and to adequately respond by inducing cell cycle arrest, senescence or apoptosis. p53 controls the cell fate at the level of different compartments, and its trafficking among organelles is modulated by different types of post-translational modifications. Thus, miss-location or sequestration of p53 within a compartment might obstruct its function as tumor suppressor leading to cell immortalization and tumorigenesis. The aim of this contribution is to give a unified overview of several reports in the literature, concerning the post-translational modifications endured by p53 which regulate its cellular trafficking and distribution at different organelles.

摘要

多种应激源——细胞内源性和外源性的——可使p53稳定并激活,通过一系列翻译后修饰(如磷酸化、乙酰化、泛素化、甲基化和类泛素化)影响p53。p53能够整合每种翻译后修饰,并通过诱导细胞周期停滞、衰老或凋亡做出充分反应。p53在不同区室水平上控制细胞命运,其在细胞器之间的运输受不同类型翻译后修饰的调节。因此,p53在某个区室内的错误定位或隔离可能会阻碍其作为肿瘤抑制因子的功能,导致细胞永生化和肿瘤发生。本论文的目的是对文献中的几篇报道进行统一概述,这些报道涉及p53所经历的翻译后修饰,这些修饰调节其在不同细胞器中的细胞运输和分布。

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