Nucleosome dynamics define transcriptional enhancers

被引:360
作者
He, Housheng Hansen [1 ,2 ,3 ,4 ]
Meyer, Clifford A. [1 ,2 ]
Shin, Hyunjin [1 ,2 ]
Bailey, Shannon T. [3 ,4 ]
Wei, Gang [5 ]
Wang, Qianben [3 ,4 ]
Zhang, Yong [1 ,2 ]
Xu, Kexin [3 ,4 ]
Ni, Min [3 ,4 ]
Lupien, Mathieu [3 ,4 ]
Mieczkowski, Piotr [6 ,7 ]
Lieb, Jason D. [6 ,7 ]
Zhao, Keji [5 ]
Brown, Myles [3 ,4 ]
Liu, X. Shirley [1 ,2 ]
机构
[1] Dana Farber Canc Inst, Dept Biostat & Computat Biol, Boston, MA 02115 USA
[2] Harvard Univ, Sch Publ Hlth, Boston, MA 02115 USA
[3] Dana Farber Canc Inst, Dept Med Oncol, Boston, MA 02115 USA
[4] Harvard Univ, Sch Med, Boston, MA USA
[5] NHLBI, Lab Mol Immunol, NIH, Bethesda, MD 20892 USA
[6] Univ N Carolina, Dept Biol, Carolina Ctr Genome Sci, Chapel Hill, NC USA
[7] Univ N Carolina, Lineberger Comprehens Canc Ctr, Chapel Hill, NC 27599 USA
基金
美国国家卫生研究院;
关键词
ANDROGEN RECEPTOR; PROSTATE-CANCER; HIGH-RESOLUTION; HUMAN GENOME; CHROMATIN-STRUCTURE; CHIP-SEQ; PROMOTERS; GENE; NKX3.1; MODEL;
D O I
10.1038/ng.545
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Chromatin plays a central role in eukaryotic gene regulation. We performed genome-wide mapping of epigenetically marked nucleosomes to determine their position both near transcription start sites and at distal regulatory elements, including enhancers. In prostate cancer cells, where androgen receptor binds primarily to enhancers, we found that androgen treatment dismisses a central nucleosome present at androgen receptor binding sites that is flanked by a pair of marked nucleosomes. A new quantitative model built on the behavior of such nucleosome pairs correctly identified regions bound by the regulators of the immediate androgen response, including androgen receptor and FOXA1. More importantly, this model also correctly predicted previously unidentified binding sites for other transcription factors present after prolonged androgen stimulation, including OCT1 and NKX3-1. Therefore, quantitative modeling of enhancer structure provides a powerful predictive method to infer the identity of transcription factors involved in cellular responses to specific stimuli.
引用
收藏
页码:343 / U101
页数:6
相关论文
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