Transcription factor binding dynamics during human ES cell differentiation

被引:263
|
作者
Tsankov, Alexander M. [1 ,2 ,3 ]
Gu, Hongcang [1 ]
Akopian, Veronika [2 ,3 ]
Ziller, Michael J. [1 ,2 ,3 ]
Donaghey, Julie [1 ,2 ,3 ]
Amit, Ido [1 ,4 ]
Gnirke, Andreas [1 ]
Meissner, Alexander [1 ,2 ,3 ]
机构
[1] Broad Inst MIT & Harvard, Cambridge, MA 02142 USA
[2] Harvard Stem Cell Inst, Cambridge, MA 02138 USA
[3] Harvard Univ, Dept Stem Cell & Regenerat Biol, Cambridge, MA 02138 USA
[4] Weizmann Inst Sci, Dept Immunol, IL-76100 Rehovot, Israel
关键词
EMBRYONIC STEM-CELLS; DNA METHYLATION; CHIP-SEQ; EPIGENOMIC ANALYSIS; REGULATORY NETWORK; SUPER-ENHANCERS; REGIONS; GENOME; STATE; SPECIFICATION;
D O I
10.1038/nature14233
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Pluripotent stem cells provide a powerful system to dissect the underlying molecular dynamics la ell fate changes during mammalian development. Here we report the integrative analysis of genome-wide binding data for 38 transcription factors with extensive epigenume and transcriptional data across the differentiation of human embryonic stem cells to the three germ layers. We describe core regulatory dynamics and show the lineage-specific behaviour of selected factors. In addition to the orchestrated remodelling of the chromatin landscape, we find that the binding of several transcription factors is strongly associated with. specific loss of DNA methylation in one germ layer, and in many cases a reciprocal gain in the other layers. Taken together, our work shows context-dependent rewiring of transcription factor binding, downstream signalling effectors, and the epigenome during human embryonic stem cell differentiation.
引用
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页码:344 / 349
页数:6
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