| Literature DB >> 27702986 |
Keshi Chen1, Qi Long1, Tao Wang1, Danyun Zhao1, Yanshuang Zhou1, Juntao Qi1, Yi Wu1, Shengbiao Li1, Chunlan Chen1, Xiaoming Zeng1, Jianguo Yang1, Zisong Zhou1, Weiwen Qin1, Xiyin Liu1, Yuxing Li1, Yingying Li1, Xiaofen Huang1, Dajiang Qin1, Jiekai Chen1, Guangjin Pan1, Hans R Schöler2, Guoliang Xu3, Xingguo Liu4, Duanqing Pei4.
Abstract
Reprogramming of somatic cells to induced pluripotent stem cells rewrites the code of cell fate at the chromatin level. Yet, little is known about this process physically. Here, we describe a fluorescence recovery after photobleaching method to assess the dynamics of heterochromatin/euchromatin and show significant heterochromatin loosening at the initial stage of reprogramming. We identify growth arrest and DNA damage-inducible protein a (Gadd45a) as a chromatin relaxer in mouse embryonic fibroblasts, which also enhances somatic cell reprogramming efficiency. We show that residue glycine 39 (G39) in Gadd45a is essential for interacting with core histones, opening chromatin and enhancing reprogramming. We further demonstrate that Gadd45a destabilizes histone-DNA interactions and facilitates the binding of Yamanaka factors to their targets for activation. Our study provides a method to screen factors that impact on chromatin structure in live cells, and identifies Gadd45a as a chromatin relaxer.Entities:
Keywords: zzm321990FRAPzzm321990; Gadd45a; chromatin relaxer; heterochromatin relaxation; reprogramming
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Year: 2016 PMID: 27702986 PMCID: PMC5090707 DOI: 10.15252/embr.201642402
Source DB: PubMed Journal: EMBO Rep ISSN: 1469-221X Impact factor: 8.807