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通过肽质量指纹图谱鉴定新型组蛋白翻译后修饰

Identification of novel histone post-translational modifications by peptide mass fingerprinting.

作者信息

Zhang Liwen, Eugeni Ericka E, Parthun Mark R, Freitas Michael A

机构信息

Department of Chemistry, The Ohio State University, Columbus, OH 43210, USA.

出版信息

Chromosoma. 2003 Aug;112(2):77-86. doi: 10.1007/s00412-003-0244-6. Epub 2003 Jul 9.

Abstract

The extent and pattern of histone post-translational modifications is a key determinant dictating the structure of chromatin. We employed mass spectrometry to map the post-translational modifications present on mammalian core histones. Using accurate peptide mass fingerprinting on proteolytic digests of purified histones, we identified more than 20 novel sites of histone modification. One newly identified site of methylation, histone H4 lysine 59, maps to the surface of the nucleosome in close proximity to the site of the only identified histone core modification, histone H3 lysine 79. Consistent with the role of histone H3 lysine 79 methylation in the formation of silent chromatin structure, histone H4 lysine 59 is essential for transcriptional silencing at the yeast silent mating loci and telomeres.

摘要

组蛋白翻译后修饰的程度和模式是决定染色质结构的关键因素。我们采用质谱法绘制了哺乳动物核心组蛋白上存在的翻译后修饰图谱。通过对纯化组蛋白的蛋白水解消化产物进行精确的肽质量指纹分析,我们鉴定出了20多个组蛋白修饰的新位点。一个新鉴定的甲基化位点,组蛋白H4赖氨酸59,位于核小体表面,紧邻唯一已鉴定的组蛋白核心修饰位点,组蛋白H3赖氨酸79。与组蛋白H3赖氨酸79甲基化在沉默染色质结构形成中的作用一致,组蛋白H4赖氨酸59对于酵母沉默交配位点和端粒处的转录沉默至关重要。

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