Opposing microRNA families regulate self-renewal in mouse embryonic stem cells

被引:537
作者
Melton, Collin [1 ,2 ]
Judson, Robert L. [1 ,2 ]
Blelloch, Robert [1 ,2 ]
机构
[1] Univ Calif San Francisco, Eli & Edythe Broad Ctr Regenerat Med & Stem Cell, Program Biomed Sci, Ctr Reprod Sci, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Dept Urol, San Francisco, CA 94143 USA
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
TRANSCRIPTIONAL NETWORK; DNA METHYLATION; C-MYC; PLURIPOTENCY; RNA; DIFFERENTIATION; EXPRESSION; LIN-28; NANOG; URIDYLATION;
D O I
10.1038/nature08725
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
When embryonic stem cells (ESCs) differentiate, they must both silence the ESC self-renewal program and activate new tissue-specific programs. In the absence of DGCR8 (Dgcr8(-/-)), a protein required for microRNA (miRNA) biogenesis, mouse ESCs are unable to silence self-renewal. Here we show that the introduction of let-7 miRNAs-a family of miRNAs highly expressed in somatic cells-can suppress self-renewal in Dgcr8(-/-) but not wild-type ESCs. Introduction of ESC cell cycle regulating (ESCC) miRNAs into the Dgcr8(-/-) ESCs blocks the capacity of let-7 to suppress self-renewal. Profiling and bioinformatic analyses show that let-7 inhibits whereas ESCC miRNAs indirectly activate numerous self-renewal genes. Furthermore, inhibition of the let-7 family promotes de-differentiation of somatic cells to induced pluripotent stem cells. Together, these findings show how the ESCC and let-7 miRNAs act through common pathways to alternatively stabilize the self-renewing versus differentiated cell fates.
引用
收藏
页码:621 / U45
页数:8
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