4.8 Article

BEND3 safeguards pluripotency by repressing differentiation-associated genes

出版社

NATL ACAD SCIENCES
DOI: 10.1073/pnas.2107406119

关键词

BEND3; differentiation; p21; promoter; transcription repression

资金

  1. NIH [GM125196, GM132458, AG065748]
  2. Cancer Center at Illinois (CCIL) Seed Grant [MCB1723008]
  3. Prairie Dragon Paddlers
  4. NSF Early-Concept Grants for Exploratory Research (EAGER) [MCB1723008]
  5. NSF [1243372, 1818286]
  6. CCIL
  7. Div Of Molecular and Cellular Bioscience
  8. Direct For Biological Sciences [1818286] Funding Source: National Science Foundation

向作者/读者索取更多资源

BEND3, a quadruple BEN domain-containing protein, is highly expressed in pluripotent cells and plays a crucial role in regulating chromatin function and transcription repression, thereby contributing to normal development and preventing differentiation.
BEN domain-containing proteins are emerging rapidly as an important class of factors involved in modulating gene expression, yet the molecular basis of how they regulate chromatin function and transcription remains to be established. BEND3 is a quadruple BEN domain-containing protein that associates with heterochromatin and functions as a transcriptional repressor. We find that BEND3 is highly expressed in pluripotent cells, and the induction of differentiation results in the down-regulation of BEND3. The removal of BEND3 from pluripotent cells results in cells exhibiting upregulation of the differentiation-inducing gene expression signature. We find that BEND3 binds to the promoters of differentiation-associated factors and key cell cycle regulators, including CDKN1A, encoding the cell cycle inhibitor p21, and represses the expression of differentiation-associated genes by enhancing H3K27me3 decoration at these promoters. Our results support a model in which transcription repression mediated by BEND3 is essential for normal development and to prevent differentiation.

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

4.8
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