Department of Cell and Developmental Biology, School of Molecular and Cellular Biology, University of Illinois at Urbana-Champaign, Urbana, IL 61801.
Developmental Therapeutics Branch, Center for Cancer Research, National Cancer Institute, Bethesda, MD 20892.
Proc Natl Acad Sci U S A. 2022 Mar 1;119(9). doi: 10.1073/pnas.2107406119.
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 , 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.
BEN 结构域蛋白作为一类重要的调节基因表达的因子正在迅速崛起,但它们如何调节染色质功能和转录的分子基础仍有待确定。BEND3 是一种四重 BEN 结构域蛋白,与异染色质相关联,并作为转录抑制剂发挥作用。我们发现 BEND3 在多能细胞中高度表达,诱导分化会导致 BEND3 的下调。从多能细胞中去除 BEND3 会导致细胞表现出分化诱导基因表达特征的上调。我们发现 BEND3 结合到分化相关因子和关键细胞周期调节剂的启动子上,包括编码细胞周期抑制剂 p21 的 ,并通过增强这些启动子上的 H3K27me3 修饰来抑制分化相关基因的表达。我们的结果支持这样一种模型,即由 BEND3 介导的转录抑制对于正常发育和防止分化是必不可少的。