miR-17-92 cluster accelerates adipocyte differentiation by negatively regulating. tumor-suppressor Rb2/p130

被引:291
作者
Wang, Qiang [1 ]
Li, Yan Chun [1 ]
Wang, Jinhua [1 ]
Kong, Juan [1 ]
Qi, Yuchen [2 ]
Quigg, Richard J. [1 ]
Li, Xinmin [1 ]
机构
[1] Univ Chicago, Dept Med, Div Biol Sci, Chicago, IL 60637 USA
[2] Beijing Univ, Coll Life Sci, Beijing 10091, Peoples R China
关键词
D O I
10.1073/pnas.0800178105
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
Adipogenesis involves cell proliferation and differentiation, both of which have been shown to be regulated by micro (mi)RNA. During mouse preadipocyte 3T3L1 cell differentiation, we found that miR-17-92, a miRNA cluster that promotes cell proliferation in various cancers, was significantly up-regulated at the clonal expansion stage of adipocyte differentiation. Stable transfection of 3T3L1 cells with miR-17-92 resulted in accelerated differentiation and increased triglyceride accumulation after hormonal stimulation. By using a luciferase reporter assay, we demonstrated that miR-17-92 directly targeted the 3' UTR region of Rb2/p130, accounting for subsequently reduced Rb2/p130 mRNA and protein quantities at the stage of clonal expansion. siRNA-mediated knock-down of Rb2/p130 at the same stage of clonal expansion recapitulated the phenotype of overexpression of miR-17-92 in the stably transfected 3T3L1 cells. These data indicate that miR-17-92 promotes adipocyte differentiation by targeting and negatively regulating Rb2/p130.
引用
收藏
页码:2889 / 2894
页数:6
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