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MAP2K6 重塑染色质,并通过激活 Gatad2b 磷酸化依赖性异染色质松弛来促进重编程。

MAP2K6 remodels chromatin and facilitates reprogramming by activating Gatad2b-phosphorylation dependent heterochromatin loosening.

机构信息

CAS Key Laboratory of Regenerative Biology, Joint School of Life Sciences, Guangzhou Institutes of Biomedicine and Health, Chinese Academy of Sciences; Bioland Laboratory (Guangzhou Regenerative Medicine and Health Guangdong Laboratory), Guangzhou Medical University, 510530, Guangzhou, China.

Guangdong Provincial Key Laboratory of Stem Cell and Regenerative Medicine, CUHK-GIBH Joint Research Laboratory on Stem Cells and Regenerative Medicine, Institute for Stem Cell and Regeneration, Guangzhou Institutes of Biomedicine and Health, Chinese Academy of Sciences, 510530, Guangzhou, China.

出版信息

Cell Death Differ. 2022 May;29(5):1042-1054. doi: 10.1038/s41418-021-00902-z. Epub 2021 Nov 24.

DOI:10.1038/s41418-021-00902-z
PMID:34815549
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9090911/
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.

摘要

体细胞重编程是研究表观遗传调控的理想模型,因为它经历了剧烈的染色质重塑。然而,磷酸化信号在染色质蛋白修饰重编程中的作用尚不清楚。在这里,我们鉴定出丝裂原活化蛋白激酶激酶 6(Mkk6)作为一种染色质松弛剂,并发现它可以显著增强重编程。Mkk6 在异染色质松弛和重编程中的功能需要其激酶活性,但不依赖于其最著名的靶标 P38。我们鉴定出 Gatad2b 是 Mkk6 磷酸化的一个新的靶标,它作为下游因子来提高组蛋白乙酰化水平并松弛异染色质。结果,Mkk6 的过表达促进了 Sox2 和 Klf4 与其靶标的结合,并在重编程过程中促进多能性基因的表达。我们的研究不仅揭示了 Mkk 磷酸化在重编程过程中对染色质状态的调节作用,而且为进一步研究和改善细胞命运决定过程提供了新的依据。

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MAP2K6 remodels chromatin and facilitates reprogramming by activating Gatad2b-phosphorylation dependent heterochromatin loosening.MAP2K6 重塑染色质,并通过激活 Gatad2b 磷酸化依赖性异染色质松弛来促进重编程。
Cell Death Differ. 2022 May;29(5):1042-1054. doi: 10.1038/s41418-021-00902-z. Epub 2021 Nov 24.
2
Correction to: MAP2K6 remodels chromatin and facilitates reprogramming by activating Gatad2b-phosphorylation dependent heterochromatin loosening.对《MAP2K6通过激活依赖Gatad2b磷酸化的异染色质松弛来重塑染色质并促进重编程》的修正
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本文引用的文献

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Protocol for detecting chromatin dynamics and screening chromatin relaxer by FRAP assay.通过 FRAP assay 检测染色质动力学和筛选染色质松弛剂的方案。
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