| First Author | Du J | Year | 2016 |
| Journal | Biochem Biophys Res Commun | Volume | 475 |
| Issue | 1 | Pages | 140-8 |
| PubMed ID | 27179777 | Mgi Jnum | J:235764 |
| Mgi Id | MGI:5800636 | Doi | 10.1016/j.bbrc.2016.05.057 |
| Citation | Du J, et al. (2016) Methylation of miR-145a-5p promoter mediates adipocytes differentiation. Biochem Biophys Res Commun 475(1):140-8 |
| abstractText | MicroRNAs (miRNAs, miR) play important roles in adipocyte development. Recent studies showed that the expression of several miRNAs is closely related with promoter methylation. However, it is not known whether miRNA mediates adipocytes differentiation by means of DNA methylation. Here, we showed that miR-145a-5p was poorly expressed in adipose tissue from mice fed a high fat diet (HFD). Overexpression or inhibition of miR-145a-5p was unfavorable or beneficial, respectively, for adipogenesis, and these effects were achieved by regulating adipocyte-specific genes involved in lipogenic transcription, fatty acid synthesis, and fatty acid transportation. Particularly, we first suggested that miR-145a-5p mimics or inhibitors promoted or repressed adipocytes proliferation by regulating p53 and p21, which act as cell cycle regulating factors. Surprisingly, the miR-145a-5p-repressed adipocyte differentiation was enhanced or rescued when cells treated with 5-Aza-dC were transfected with miR-145a-5p mimics or inhibitors, respectively. These data indicated that, as a new mean to positively regulate adipocyte proliferation, the process of miR-145a-5p-inhibited adipogenesis may be regulated by DNA methylation. |
