4.8 Article

Three Distinct Patterns of Histone H3Y41 Phosphorylation Mark Active Genes

期刊

CELL REPORTS
卷 2, 期 3, 页码 470-477

出版社

CELL PRESS
DOI: 10.1016/j.celrep.2012.08.016

关键词

-

资金

  1. Cancer Research UK
  2. Leukaemia & Lymphoma Research UK
  3. UK Medical Research Council
  4. Wellcome Trust
  5. Leukemia & Lymphoma Society of America
  6. NIHR Cambridge Biomedical Research Centre
  7. 6th Research Framework Programme of the European Union (Epitron and SMARTER)
  8. Biotechnology and Biological Sciences Research Council [BB/I00050X/1] Funding Source: researchfish
  9. Cancer Research UK [12765] Funding Source: researchfish
  10. Medical Research Council [G0800784B, G0800784] Funding Source: researchfish
  11. National Centre for the Replacement, Refinement and Reduction of Animals in Research (NC3Rs) [G0900729/1] Funding Source: researchfish
  12. BBSRC [BB/I00050X/1] Funding Source: UKRI
  13. MRC [G0800784] Funding Source: UKRI

向作者/读者索取更多资源

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.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.8
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据