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组蛋白修饰作为转录的关键调节因子。

Histone modifications as key regulators of transcription.

作者信息

Khan Asad U, Krishnamurthy Shankarling

机构信息

Interdisciplinary Biotechnology Unit, Aligarh Muslim University, Aligarh 202002 India.

出版信息

Front Biosci. 2005 Jan 1;10:866-72. doi: 10.2741/1580.

DOI:10.2741/1580
PMID:15569624
Abstract

Covalent modifications of the amino-termini of the core histones in nucleosomes have been shown to be one of the key regulatory mechanisms in transcription regulation. Recently, new roles for histone modifications have been uncovered for the efficient functioning of RNA Pol II. Besides acetylation, which is the most characterized to date these modifications comprise phosphorylation, methylation, and ubiquitination. This review gives comprehensive view of all the major histone modifications and their effect on transcriptional regulation, in Saccharomyces cerevisiae.

摘要

核小体中核心组蛋白氨基末端的共价修饰已被证明是转录调控中的关键调节机制之一。最近,人们发现组蛋白修饰在RNA聚合酶II的有效功能中具有新的作用。除了乙酰化(这是迄今为止研究最多的修饰)外,这些修饰还包括磷酸化、甲基化和泛素化。本文综述了酿酒酵母中所有主要的组蛋白修饰及其对转录调控的影响。

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Histone modifications as key regulators of transcription.组蛋白修饰作为转录的关键调节因子。
Front Biosci. 2005 Jan 1;10:866-72. doi: 10.2741/1580.
2
H2B-K123 ubiquitination stimulates RNAPII elongation independent of H3-K4 methylation.H2B赖氨酸123位的泛素化可刺激RNA聚合酶II的延伸,且不依赖于H3赖氨酸4位的甲基化。
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A site to remember: H3K36 methylation a mark for histone deacetylation.一个值得铭记的位点:H3K36甲基化——组蛋白去乙酰化的一个标记
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RSC exploits histone acetylation to abrogate the nucleosomal block to RNA polymerase II elongation.RSC利用组蛋白乙酰化来消除核小体对RNA聚合酶II延伸的阻碍。
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