The Polycomb Protein Ezh2 Impacts on Induced Pluripotent Stem Cell Generation

被引:49
作者
Ding, Xiaolei [1 ,2 ]
Wang, Xiaoying [1 ,2 ]
Sontag, Stephanie [1 ,2 ]
Qin, Jie [1 ,2 ]
Wanek, Paul [1 ,2 ]
Lin, Qiong [1 ,2 ]
Zenke, Martin [1 ,2 ]
机构
[1] Rhein Westfal TH Aachen, Sch Med, Inst Biomed Engn, Dept Cell Biol, D-52074 Aachen, Germany
[2] Rhein Westfal TH Aachen, Helmholtz Inst Biomed Engn, D-52074 Aachen, Germany
关键词
GROUP GENE EZH2; SOMATIC-CELLS; DEVELOPMENTAL REGULATORS; EPIGENETIC REGULATION; DIFFERENTIATED CELLS; IPS CELLS; CHROMATIN; EXPRESSION; PRC2; METHYLATION;
D O I
10.1089/scd.2013.0267
中图分类号
Q813 [细胞工程];
学科分类号
100113 [医学细胞生物学];
摘要
Reprogramming of somatic cells toward pluripotency involves extensive chromatin reorganization and changes in gene expression. Polycomb group (PcG) proteins are key regulators of chromatin structure, cell identity, and development. In this study, we investigated the impact of Ezh2, a core subunit of Polycomb repressive complex 2 (PRC2), on the generation of induced pluripotent stem (iPS) cells. We found that Ezh2 expression is induced during iPS cell generation and iPS cells contain high levels of Ezh2 mRNA and protein. Importantly, shRNA knockdown of Ezh2 during reprogramming severely impairs iPS cell generation. Mechanistically, Ezh2 acts during reprogramming at least in part through repressing the Ink4a/Arf locus, which represents a major roadblock for iPS cell generation. Interestingly, knockdown of Ezh2 in established pluripotent cells leaves pluripotency and self-renewal of embryonic stem cells and iPS cells unaffected. Altogether, our results demonstrate that Ezh2 is critical for efficient iPS cell generation, whereas it is dispensable for maintaining the reprogrammed iPS cell state.
引用
收藏
页码:931 / 940
页数:10
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