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本文引用的文献

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Nucleosome assembly and epigenetic inheritance.核小体组装与表观遗传遗传。
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2
Partitioning of histone H3-H4 tetramers during DNA replication-dependent chromatin assembly.组蛋白 H3-H4 四聚体在 DNA 复制依赖性染色质组装过程中的分配。
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Chromatin structure and the inheritance of epigenetic information.染色质结构与表观遗传信息的传递。
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MSQuant, an open source platform for mass spectrometry-based quantitative proteomics.MSQuant,一个基于质谱的定量蛋白质组学的开源平台。
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Role of the polycomb protein EED in the propagation of repressive histone marks.多梳蛋白EED在抑制性组蛋白标记传播中的作用。
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Epigenetic inheritance during the cell cycle.细胞周期中的表观遗传继承。
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Histone crosstalk between H2B monoubiquitination and H3 methylation mediated by COMPASS.由COMPASS介导的H2B单泛素化与H3甲基化之间的组蛋白串扰。
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Arginine methylation at histone H3R2 controls deposition of H3K4 trimethylation.组蛋白H3第2位精氨酸的甲基化调控H3K4三甲基化的沉积。
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组蛋白赖氨酸甲基化不需要核小体内部的全局对称修饰。

Symmetrical modification within a nucleosome is not required globally for histone lysine methylation.

机构信息

Life Science College, Beijing Normal University, Beijing 100875, China.

出版信息

EMBO Rep. 2011 Mar;12(3):244-51. doi: 10.1038/embor.2011.6. Epub 2011 Feb 18.

DOI:10.1038/embor.2011.6
PMID:21331095
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3059902/
Abstract

Two copies of each core histone exist in every nucleosome; however, it is not known whether both histones within a nucleosome are required to be symmetrically methylated at the same lysine residues. We report that for most lysine methylation states, wild-type histones paired with mutant, unmethylatable histones in mononucleosomes have comparable methylation levels to bulk histones. Our results indicate that symmetrical histone methylation is not required on a global scale. However, wild-type H4 histones paired with unmethylatable H4K20R histones showed reduced levels of H4K20me2 and H4K20me3, suggesting that some fractions of these modifications might exist symmetrically, and enzymes mediating these modifications might, to some extent, favour nucleosome substrates with premethylated H4K20.

摘要

每个核小体中存在两份每种核心组蛋白;然而,尚不清楚核小体中的两个组蛋白是否都需要在相同的赖氨酸残基上对称地甲基化。我们报告说,对于大多数赖氨酸甲基化状态,在单核小体中,野生型组蛋白与突变的、不可甲基化的组蛋白配对具有与整体组蛋白相当的甲基化水平。我们的结果表明,全局范围内不需要对称的组蛋白甲基化。然而,野生型 H4 组蛋白与不可甲基化的 H4K20R 组蛋白配对显示出 H4K20me2 和 H4K20me3 的水平降低,这表明这些修饰的某些部分可能是对称存在的,并且介导这些修饰的酶可能在某种程度上偏爱具有预甲基化 H4K20 的核小体底物。