Wang Zhibin, Zang Chongzhi, Rosenfeld Jeffrey A, Schones Dustin E, Barski Artem, Cuddapah Suresh, Cui Kairong, Roh Tae-Young, Peng Weiqun, Zhang Michael Q, Zhao Keji
Laboratory of Molecular Immunology, National Heart, Lung, and Blood Institute, US National Institutes of Health, Bethesda, Maryland 20892, USA.
Nat Genet. 2008 Jul;40(7):897-903. doi: 10.1038/ng.154. Epub 2008 Jun 15.
Histones are characterized by numerous posttranslational modifications that influence gene transcription. However, because of the lack of global distribution data in higher eukaryotic systems, the extent to which gene-specific combinatorial patterns of histone modifications exist remains to be determined. Here, we report the patterns derived from the analysis of 39 histone modifications in human CD4(+) T cells. Our data indicate that a large number of patterns are associated with promoters and enhancers. In particular, we identify a common modification module consisting of 17 modifications detected at 3,286 promoters. These modifications tend to colocalize in the genome and correlate with each other at an individual nucleosome level. Genes associated with this module tend to have higher expression, and addition of more modifications to this module is associated with further increased expression. Our data suggest that these histone modifications may act cooperatively to prepare chromatin for transcriptional activation.
组蛋白的特征是存在大量影响基因转录的翻译后修饰。然而,由于高等真核生物系统中缺乏全局分布数据,组蛋白修饰的基因特异性组合模式存在的程度仍有待确定。在这里,我们报告了对人类CD4(+) T细胞中39种组蛋白修饰分析得出的模式。我们的数据表明,大量模式与启动子和增强子相关。特别是,我们鉴定出一个由在3286个启动子处检测到的17种修饰组成的常见修饰模块。这些修饰倾向于在基因组中共定位,并且在单个核小体水平上相互关联。与该模块相关的基因往往具有更高的表达,并且向该模块添加更多修饰与进一步增加的表达相关。我们的数据表明,这些组蛋白修饰可能协同作用,为转录激活准备染色质。