| Literature DB >> 25936917 |
Junjun Ding1, Xin Huang1, Ningyi Shao2, Hongwei Zhou1, Dung-Fang Lee1, Francesco Faiola1, Miguel Fidalgo1, Diana Guallar1, Arven Saunders3, Pavel V Shliaha4, Hailong Wang5, Avinash Waghray3, Dmitri Papatsenko1, Carlos Sánchez-Priego1, Dan Li3, Ye Yuan3, Ihor R Lemischka6, Li Shen2, Kevin Kelley7, Haiteng Deng8, Xiaohua Shen8, Jianlong Wang9.
Abstract
Super-enhancers (SEs) are large clusters of transcriptional enhancers that are co-occupied by multiple lineage-specific transcription factors driving expression of genes that define cell identity. In embryonic stem cells (ESCs), SEs are highly enriched for the core pluripotency factors Oct4, Sox2, and Nanog. In this study, we sought to dissect the molecular control mechanism of SE activity in pluripotency and reprogramming. Starting from a protein interaction network surrounding Sox2, we identified Tex10 as a key pluripotency factor that plays a functionally significant role in ESC self-renewal, early embryo development, and reprogramming. Tex10 is enriched at SEs in a Sox2-dependent manner and coordinates histone acetylation and DNA demethylation at SEs. Tex10 activity is also important for pluripotency and reprogramming in human cells. Our study therefore highlights Tex10 as a core component of the pluripotency network and sheds light on its role in epigenetic control of SE activity for cell fate determination.Entities:
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Year: 2015 PMID: 25936917 PMCID: PMC4458159 DOI: 10.1016/j.stem.2015.04.001
Source DB: PubMed Journal: Cell Stem Cell ISSN: 1875-9777 Impact factor: 24.633