Journal of Biological ChemistryDevelopmental BiologyPeer-reviewed journal article
CTCF-binding element regulates ESC differentiation via orchestrating long-range chromatin interaction between enhancers and HoxA
Guangsong SuiD, Wenbin WangiD, Jun CheniD, Man LiuiD, Jian Zheng, Dianhao Guo, Jinfang Bi, Zhongfang Zhao, Jiandang ShiiD, Lei ZhangiD, Wange LuiD
Abstract
Proper expressions of Homeobox A cluster genes (HoxA) are essential for embryonic stem cells (ESC) differentiation and individual development. However, the mechanisms underlying controlling precise spatiotemporal expressions of HoxA during early ESC differentiation remain poorly understood. Herein, we identified a functional CTCF-binding element (CBE+47) closest to the 3-end of HoxA within the same topologically associated domain (TAD) in ESC. CRISPR-Cas9 mediated the CBE+47 deletion significantly promotes retinoic acid (RA)-induced HoxA expression and early ESC abnormal differentiation. In delineating its underlying mechanisms, we find that CBE+47 can precisely organize chromatin interactions between its adjacent enhancers and HoxA by using chromosome conformation capture assay (Capture-C). Furthermore, we also find that its adjacent enhancers as enhancer-enhancer interaction complex (EEIC) are required for RA-induced HoxA activation. Collectively, these results provide a new insight for RA-induced HoxA expression, also highlight the unique and precise regulatory roles of CBE in ESC differentiation.
- organism: mouse
- assay: ChIP-seq
- assay: Hi-C
- research focus: gene regulatory network inference
- research focus: differential expression
- research focus: spatial domain detection
- approach: statistical model
- approach: experimental assay
- Citations
- 14
- FWCI
- 0.71
- Field percentile
- top 36%
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