Chromatin proteomic profiling reveals novel proteins associated with histone-marked genomic regions

被引:108
作者
Ji, Xiong [1 ]
Dadon, Daniel B. [1 ,2 ]
Abraham, Brian J. [1 ]
Lee, Tong Ihn [1 ]
Jaenisch, Rudolf [1 ,2 ]
Bradner, James E. [3 ,4 ]
Young, Richard A. [1 ,2 ]
机构
[1] Whitehead Inst Biomed Res, Cambridge, MA 02142 USA
[2] MIT, Dept Biol, Cambridge, MA 02139 USA
[3] Dana Farber Canc Inst, Dept Med Oncol, Boston, MA 02115 USA
[4] Harvard Univ, Sch Med, Dept Med, Boston, MA 02115 USA
基金
美国国家卫生研究院;
关键词
chromatin; genomics; proteomics; TRANSCRIPTION FACTORS; MASS SPECTROMETRY; SUPER-ENHANCERS; CELL IDENTITY; RNA; CANCER; PSEUDOURIDYLATION; DEMETHYLATION; EPIGENETICS; EXPRESSION;
D O I
10.1073/pnas.1502971112
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
More than a thousand proteins are thought to contribute to mammalian chromatin and its regulation, but our understanding of the genomic occupancy and function of most of these proteins is limited. Here we describe an approach, which we call "chromatin proteomic profiling," to identify proteins associated with genomic regions marked by specifically modified histones. We used ChIP-MS to identify proteins associated with genomic regions marked by histones modified at specific lysine residues, including H3K27ac, H3K4me3, H3K79me2, H3K36me3, H3K9me3, and H4K20me3, in ES cells. We identified 332 known and 114 novel proteins associated with these histone-marked genomic segments. Many of the novel candidates have been implicated in various diseases, and their chromatin association may provide clues to disease mechanisms. More than 100 histone modifications have been described, so similar chromatin proteomic profiling studies should prove to be valuable for identifying many additional chromatin-associated proteins in a broad spectrum of cell types.
引用
收藏
页码:3841 / 3846
页数:6
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