| Literature DB >> 35385732 |
Yawei Song1, Zhengyu Liang2, Jie Zhang3, Gongcheng Hu1, Juehan Wang3, Yaoyi Li1, Rong Guo3, Xiaotao Dong1, Isaac A Babarinde4, Wangfang Ping3, Ying-Liang Sheng5, Huanhuan Li6, Zhaoming Chen7, Minghui Gao6, Yang Chen8, Ge Shan9, Michael Q Zhang10, Andrew P Hutchins4, Xiang-Dong Fu11, Hongjie Yao12.
Abstract
CTCF mediates chromatin insulation and long-distance enhancer-promoter (EP) interactions; however, little is known about how these regulatory functions are partitioned among target genes in key biological processes. Here, we show that Ctcf expression is progressively increased during induced pluripotency. In this process, CTCF first functions as a chromatin insulator responsible for direct silencing of the somatic gene expression program and, interestingly, elevated Ctcf expression next ensures chromatin accessibility and contributes to increased EP interactions for a fraction of pluripotency-associated genes. Therefore, CTCF functions in a context-specific manner to modulate the 3D genome to enable cellular reprogramming. We further discover that these context-specific CTCF functions also enlist SMARCA5, an imitation switch (ISWI) chromatin remodeler, together rewiring the epigenome to facilitate cell-fate switch. These findings reveal the dual functions of CTCF in conjunction with a key chromatin remodeler to drive reprogramming toward pluripotency.Entities:
Keywords: CP: Molecular biology; CP: Stem cell research; CTCF; SMARCA5; chromatin accessibility; chromatin insulation; enhancer-promoter interactions; reprogramming
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Year: 2022 PMID: 35385732 DOI: 10.1016/j.celrep.2022.110626
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423