| Literature DB >> 34815549 |
Guangsuo Xing1,2, Zichao Liu1,2,3, Luyuan Huang1,2,3, Danyun Zhao1,2,3, Tao Wang1,2, Hao Yuan1,2, Yi Wu1,2, Linpeng Li1,2, Qi Long1,2, Yanshuang Zhou1,2, Zhihong Hao1,2,3, Yang Liu1,2,3, Jianghuan Lu1,2, Shiting Li1,2, Jieying Zhu1,2, Bo Wang1,2, Junwei Wang1,2, Jing Liu1,2, Jiekai Chen1,2, Duanqing Pei4,5,6, Xingguo Liu7,8,9, Keshi Chen10,11.
Abstract
Somatic cell reprogramming is an ideal model for studying epigenetic regulation as it undergoes dramatic chromatin remodeling. However, a role for phosphorylation signaling in chromatin protein modifications for reprogramming remains unclear. Here, we identified mitogen-activated protein kinase kinase 6 (Mkk6) as a chromatin relaxer and found that it could significantly enhance reprogramming. The function of Mkk6 in heterochromatin loosening and reprogramming requires its kinase activity but does not depend on its best-known target, P38. We identified Gatad2b as a novel target of Mkk6 phosphorylation that acts downstream to elevate histone acetylation levels and loosen heterochromatin. As a result, Mkk6 over-expression facilitates binding of Sox2 and Klf4 to their targets and promotes pluripotency gene expression during reprogramming. Our studies not only reveal an Mkk phosphorylation mediated modulation of chromatin status in reprogramming, but also provide new rationales to further investigate and improve the cell fate determination processes.Entities:
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Year: 2021 PMID: 34815549 PMCID: PMC9090911 DOI: 10.1038/s41418-021-00902-z
Source DB: PubMed Journal: Cell Death Differ ISSN: 1350-9047 Impact factor: 12.067