4.7 Article

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

Journal

CELL DEATH AND DIFFERENTIATION
Volume 29, Issue 5, Pages 1042-1054

Publisher

SPRINGERNATURE
DOI: 10.1038/s41418-021-00902-z

Keywords

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Funding

  1. National Key Research and Development Program of China [2018YFA0107100, 2017YFA0106300, 2017YFA0102900, 2017YFA0504100, 2019YFA09004500]
  2. Strategic Priority Research Program of the Chinese Academy of Sciences [XDA16030505]
  3. National Natural Science Foundation projects of China [32025010, 31900614, 31970709, 81901275, 32070729, 32100619, 32170747, 31830060]
  4. Key Research Program of Frontier Sciences, CAS [QYZDB-SSW-SMC001]
  5. International Cooperation Program, CAS [154144KYSB20200006]
  6. Guangdong Province Science and Technology Program [2020B1212060052, 2018A030313825, 2018GZR110103002, 2020A1515011200, 2020A1515010919, 2020A1515011410, 2021A1515012513]
  7. Guangzhou Science and Technology Program [201807010067, 202002030277, 202102020827, 202102080066]
  8. Open Research Program of Key Laboratory of Regenerative Biology, CAS [KLRB201907, KLRB202014]
  9. CAS Youth Innovation Promotion Association

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The study revealed that Mkk6 acts as a chromatin relaxer during reprogramming by promoting histone acetylation levels and facilitating transcription factor binding, ultimately enhancing pluripotency gene expression.
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.

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