目前对组蛋白磷酸化在调节染色质生物学中的重要性的认识。

Beatriz Pérez-Cadahía, Bojan Drobic, Protiti Khan, Chaitra C Shivashankar, James R Davie
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引用次数: 0

摘要

核心组蛋白H2A、H2B、H3和H4发生各种翻译后修饰,如乙酰化、甲基化和磷酸化。核心组蛋白磷酸化参与多种生物反应,包括转录、有丝分裂、DNA修复和细胞凋亡。组蛋白磷酸化可能破坏染色质结构和/或为非组蛋白染色体蛋白募集或阻断染色质提供“密码”。在较好表征的组蛋白磷酸化事件中,H3在Ser10和Ser 28位点的磷酸化,以及H2A变体H2A的磷酸化。Ser139处的X。染色质中许多其他核心组蛋白磷酸化事件的功能仍有待了解。本文综述了核心组蛋白磷酸化在哺乳动物细胞中的生物学作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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Current understanding and importance of histone phosphorylation in regulating chromatin biology.

The core histones H2A, H2B, H3 and H4, undergo various post-translational modifications, such as acetylation, methylation and phosphorylation. Core histone phosphorylation has roles in several biological responses, including transcription, mitosis, DNA repair and apoptosis. Histone phosphorylation may disrupt chromatin structure and/or provide a 'code' for the recruitment or occlusion of non-histone chromosomal proteins to chromatin. Among the better-characterized histone phosphorylation events are the phosphorylation of H3 at Ser10 and Ser 28, and the phosphorylation of the H2A variant H2A.X at Ser139. Much remains to be learned about the function of the many other core histone phosphorylation events in chromatin. This review provides an overview of the biological roles of core histone phosphorylation in mammalian cells.

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