miR-294/miR-302 Promotes Proliferation, Suppresses G1-S Restriction Point, and Inhibits ESC Differentiation through Separable Mechanisms

被引:101
作者
Wang, Yangming [1 ,2 ,3 ]
Melton, Collin [2 ,3 ]
Li, Ya-Pu [1 ]
Shenoy, Archana [2 ,3 ]
Zhang, Xin-Xin [1 ]
Subramanyam, Deepa [2 ,3 ]
Blelloch, Robert [2 ,3 ]
机构
[1] Peking Univ, Peking Tsinghua Joint Ctr Life Sci, Inst Mol Med, Beijing 100871, Peoples R China
[2] Univ Calif San Francisco, Dept Urol, Ctr Reprod Sci, San Francisco, CA 94143 USA
[3] Univ Calif San Francisco, Eli & Edythe Broad Ctr Regenerat Med & Stem Cell, 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
EMBRYONIC STEM-CELLS; SELF-RENEWAL; CYCLE REGULATION; MICRORNA BIOGENESIS; MATURE MICRORNAS; MOUSE; PLURIPOTENCY; TRANSITION; EXPRESSION; FIBROBLASTS;
D O I
10.1016/j.celrep.2013.05.027
中图分类号
Q2 [细胞生物学];
学科分类号
071013 [干细胞生物学];
摘要
The miR-294 and miR-302 microRNAs promote the abbreviated G1 phase of the embryonic stem cell (ESC) cell cycle and suppress differentiation induced by let-7. Here, we evaluated the role of the retinoblastoma (Rb) family proteins in these settings. Under normal growth conditions, miR-294 promoted the rapid G1-S transition independent of the Rb family. In contrast, miR-294 suppressed the further accumulation of cells in G1 in response to nutrient deprivation and cell-cell contact in an Rb-dependent fashion. We uncovered five additional miRNAs (miR-26a, miR-99b, miR-193, miR-199a-5p, and miR-218) that silenced ESC self-renewal in the absence of other miRNAs, all of which were antagonized by miR-294 and miR-302. Four of the six differentiation-inducing miRNAs induced an Rb-dependent G1 accumulation. However, all six still silenced self-renewal in the absence of the Rb proteins. These results show that the miR-294/miR-302 family acts through Rb-dependent and -independent pathways to regulate the G1 restriction point and the silencing of self-renewal, respectively.
引用
收藏
页码:99 / 109
页数:11
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