Trim71 cooperates with microRNAs to repress Cdkn1a expression and promote embryonic stem cell proliferation

被引:126
作者
Chang, Hao-Ming [1 ]
Martinez, Natalia J. [1 ]
Thornton, James E. [1 ]
Hagan, John P. [1 ]
Nguyen, Khang D. [1 ]
Gregory, Richard I. [1 ]
机构
[1] Harvard Univ, Childrens Hosp Boston, Sch Med,Harvard Stem Cell Inst, Stem Cell Program,Dept Biol Chem & Mol Pharmacol, Boston, MA 02115 USA
来源
NATURE COMMUNICATIONS | 2012年 / 3卷
基金
美国国家科学基金会;
关键词
SELF-RENEWAL; LET-7; MICRORNA; TARGET GENE; BRAIN-TUMOR; MOUSE; LIN-41; BIOGENESIS; ARGONAUTE2; PATHWAY; MEI-P26;
D O I
10.1038/ncomms1909
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
Pluripotent embryonic stem cells have a shortened cell cycle that enables their rapid proliferation. The embryonic stem cell-specific miR-290 and miR-302 microRNA families promote proliferation whereas let-7 microRNAs inhibit self-renewal, and promote cell differentiation. Lin28 suppresses let-7 expression in embryonic stem cells. Here to gain further insight into mechanisms controlling embryonic stem cell self-renewal, we explore the molecular and cellular role of the let-7 target Trim71 (mLin41). We show that Trim71 associates with Argonaute2 and microRNAs, and represses expression of Cdkn1a, a cyclin-dependent kinase inhibitor that negatively regulates the G1-S transition. We identify protein domains required for Trim71 association with Argonaute2, localization to P-bodies, and for repression of reporter messenger RNAs. Trim71 knockdown prolongs the G1 phase of the cell cycle and slows embryonic stem cell proliferation, a phenotype that was rescued by depletion of Cdkn1a. Thus, we demonstrate that Trim71 is a factor that facilitates the G1-S transition to promote rapid embryonic stem cell self-renewal.
引用
收藏
页数:10
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