Three Distinct Patterns of Histone H3Y41 Phosphorylation Mark Active Genes

被引:53
作者
Dawson, Mark A. [1 ,2 ,3 ,4 ,5 ,6 ]
Foster, Samuel D. [1 ,2 ,3 ]
Bannister, Andrew J. [4 ,5 ]
Robson, Samuel C. [4 ,5 ]
Hannah, Rebecca [1 ,2 ,3 ]
Wang, Xiaonan [1 ,2 ,3 ]
Xhemalce, Blerta [4 ,5 ]
Wood, Andrew D. [1 ,2 ,3 ]
Green, Anthony R. [1 ,2 ,3 ,6 ]
Goettgens, Berthold [1 ,2 ,3 ]
Kouzarides, Tony [4 ,5 ]
机构
[1] Univ Cambridge, Cambridge Inst Med Res, Dept Haematol, Cambridge CB2 0XY, England
[2] Univ Cambridge, Wellcome Trust, Cambridge CB2 0XY, England
[3] Univ Cambridge, MRC Stem Cell Inst, Cambridge CB2 0XY, England
[4] Gurdon Inst, Cambridge CB2 1QN, England
[5] Dept Pathol, Cambridge CB2 1QN, England
[6] Univ Cambridge, Addenbrookes Hosp, Cambridge CB2 0XY, England
基金
英国生物技术与生命科学研究理事会; 英国惠康基金; 英国医学研究理事会;
关键词
STAT5; BINDING; PROTEIN; JAK2; EXPRESSION; LEUKEMIA; TARGET; CELLS; CIS;
D O I
10.1016/j.celrep.2012.08.016
中图分类号
Q2 [细胞生物学];
学科分类号
071013 [干细胞生物学];
摘要
The JAK2 tyrosine kinase is a critical mediator of cytokine-induced signaling. It plays a role in the nucleus, where it regulates transcription by phosphorylating histone H3 at tyrosine 41 (H3Y41ph). We used chromatin immunoprecipitation coupled to massively parallel DNA sequencing (ChIP-seq) to define the genome-wide pattern of H3Y41ph in human erythroid leukemia cells. Our results indicate that H3Y41ph is located at three distinct sites: (1) at a subset of active promoters, where it overlaps with H3K4me3, (2) at distal cis-regulatory elements, where it coincides with the binding of STAT5, and (3) throughout the transcribed regions of active, tissue-specific hematopoietic genes. Together, these data extend our understanding of this conserved and essential signaling pathway and provide insight into the mechanisms by which extracellular stimuli may lead to the coordinated regulation of transcription.
引用
收藏
页码:470 / 477
页数:8
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