4.6 Article

Chd5 Regulates MuERV-L/MERVL Expression in Mouse Embryonic Stem Cells Via H3K27me3 Modification and Histone H3.1/H3.2

期刊

JOURNAL OF CELLULAR BIOCHEMISTRY
卷 117, 期 3, 页码 780-792

出版社

WILEY
DOI: 10.1002/jcb.25368

关键词

CHROMATIN REMODELING ENZYME; Chd5; RETROTRANSPOSON; STEM CELL BIOLOGY

资金

  1. Japan Society for the Promotion of Science (JSPS) [25116010, 26290064]
  2. Grants-in-Aid for Scientific Research [15K15365, 15K18457, 13J04024, 25116010, 25503003, 25840087, 24118002] Funding Source: KAKEN

向作者/读者索取更多资源

Chd5 is an essential factor for neuronal differentiation and spermatogenesis and is a known tumor suppressor. H3K27me3 and H3K4un are modifications recognized by Chd5; however, it remains unclear how Chd5 remodels chromatin structure. We completely disrupted the Chd5 locus using the CRISPR-Cas9 system to generate a 52 kbp long deletion and analyzed Chd5 function in mouse embryonic stem cells. Our findings show that Chd5 represses murine endogenous retrovirus-L (MuERV-L/MERVL), an endogenous retrovirus-derived retrotransposon, by regulating H3K27me3 and H3.1/H3.2 function. (C) 2015 Wiley Periodicals, Inc.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.6
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据