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

miR-17-92 cluster accelerates adipocyte differentiation by negatively regulating tumor-suppressor Rb2/p130
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.
- University of Chicago United States
- Beijing Information Science & Technology University China (People's Republic of)
- University of Chicago Medical Center United States
- China University of Petroleum, Beijing China (People's Republic of)
Retinoblastoma-Like Protein p130, Reverse Transcriptase Polymerase Chain Reaction, Blotting, Western, Cell Differentiation, Mice, MicroRNAs, Gene Expression Regulation, 3T3-L1 Cells, Adipocytes, Animals, RNA Interference, RNA, Small Interfering, Luciferases, 3' Untranslated Regions, Azo Compounds, DNA Primers
Retinoblastoma-Like Protein p130, Reverse Transcriptase Polymerase Chain Reaction, Blotting, Western, Cell Differentiation, Mice, MicroRNAs, Gene Expression Regulation, 3T3-L1 Cells, Adipocytes, Animals, RNA Interference, RNA, Small Interfering, Luciferases, 3' Untranslated Regions, Azo Compounds, DNA Primers
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