生物
组蛋白甲基转移酶
组蛋白甲基化
表观遗传学
遗传学
组蛋白密码
染色质
组蛋白H2A
组蛋白
组蛋白H1
EZH2型
分子生物学
核小体
DNA甲基化
基因
基因表达
作者
Artem Barski,Suresh Cuddapah,Kairong Cui,Tae‐Young Roh,Dustin E. Schones,Zhibin Wang,Gang Wei,Iouri Chepelev,Keji Zhao
出处
期刊:Cell
[Elsevier]
日期:2007-05-01
卷期号:129 (4): 823-837
被引量:6178
标识
DOI:10.1016/j.cell.2007.05.009
摘要
Histone modifications are implicated in influencing gene expression. We have generated high-resolution maps for the genome-wide distribution of 20 histone lysine and arginine methylations as well as histone variant H2A.Z, RNA polymerase II, and the insulator binding protein CTCF across the human genome using the Solexa 1G sequencing technology. Typical patterns of histone methylations exhibited at promoters, insulators, enhancers, and transcribed regions are identified. The monomethylations of H3K27, H3K9, H4K20, H3K79, and H2BK5 are all linked to gene activation, whereas trimethylations of H3K27, H3K9, and H3K79 are linked to repression. H2A.Z associates with functional regulatory elements, and CTCF marks boundaries of histone methylation domains. Chromosome banding patterns are correlated with unique patterns of histone modifications. Chromosome breakpoints detected in T cell cancers frequently reside in chromatin regions associated with H3K4 methylations. Our data provide new insights into the function of histone methylation and chromatin organization in genome function.
科研通智能强力驱动
Strongly Powered by AbleSci AI