DGCR8 is essential for microRNA biogenesis and silencing of embryonic stem cell self-renewal

被引:756
作者
Wang, Yangming
Medvid, Rostislav
Melton, Collin
Jaenisch, Rudolf
Blelloch, Robert [1 ]
机构
[1] Univ Calif San Francisco, Dept Urol, Dev & Stem Cell Biol Program, San Francisco, CA 94143 USA
[2] Whitehead Inst Biomed Res, Cambridge, MA 02142 USA
关键词
D O I
10.1038/ng1969
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The molecular controls that govern the differentiation of embryonic stem (ES) cells remain poorly understood. DGCR8 is an RNA-binding protein that assists the RNase III enzyme Drosha in the processing of microRNAs (miRNAs), a subclass of small RNAs. Here we study the role of miRNAs in ES cell differentiation by generating a Dgcr8 knockout model. Analysis of mouse knockout ES cells shows that DGCR8 is essential for biogenesis of miRNAs. On the induction of differentiation, DGCR8-deficient ES cells do not fully downregulate pluripotency markers and retain the ability to produce ES cell colonies; however, they do express some markers of differentiation. This phenotype differs from that reported for Dicer1 knockout cells, suggesting that Dicer has miRNA-independent roles in ES cell function. Our findings indicate that miRNAs function in the silencing of ES cell self-renewal that normally occurs with the induction of differentiation.
引用
收藏
页码:380 / 385
页数:6
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