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自噬中的乙酰化新靶点。

New targets for acetylation in autophagy.

机构信息

INSERM U984, University Paris-Sud 11, 92296 Châtenay-Malabry, France.

出版信息

Sci Signal. 2012 Jul 3;5(231):pe29. doi: 10.1126/scisignal.2003187.

Abstract

Macroautophagy is an evolutionarily conserved homeostatic process that mediates the degradation of long-lived cytoplasmic components in eukaryotes, which allows cells to survive stresses such as inflammation, hypoxia, and deprivation of nutrients or growth factors. At least 30 members of the Atg (autophagy-related) protein family orchestrate this degradative process. Additional complexity resides in the signaling networks controlling the autophagic process, which include various posttranslational modifications of key components. Evidence is accumulating that protein acetylation represents an evolutionarily conserved mechanism tightly regulating macroautophagy.

摘要

自噬是一种进化上保守的稳态过程,它介导真核生物中长寿细胞质成分的降解,使细胞能够在炎症、缺氧、营养物质或生长因子缺乏等应激条件下存活。至少有 30 种 Atg(自噬相关)蛋白家族成员协调这一降解过程。控制自噬过程的信号网络的复杂性还在于包括关键成分的各种翻译后修饰。越来越多的证据表明,蛋白质乙酰化代表了一种进化上保守的机制,可严格调节巨自噬。

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