| First Author | Yi SA | Year | 2016 |
| Journal | Mol Cell | Volume | 62 |
| Issue | 3 | Pages | 443-452 |
| PubMed ID | 27151441 | Mgi Jnum | J:248788 |
| Mgi Id | MGI:6093977 | Doi | 10.1016/j.molcel.2016.03.011 |
| Citation | Yi SA, et al. (2016) S6K1 Phosphorylation of H2B Mediates EZH2 Trimethylation of H3: A Determinant of Early Adipogenesis. Mol Cell 62(3):443-452 |
| abstractText | S6K1 has been implicated in a number of key metabolic responses, which contribute to obesity. Critical among these is the control of a transcriptional program required for the commitment of mesenchymal stem cells to the adipocytic lineage. However, in contrast to its role in the cytosol, the functions and targets of nuclear S6K1 are unknown. Here, we show that adipogenic stimuli trigger nuclear translocation of S6K1, leading to H2BS36 phosphorylation and recruitment of EZH2 to H3, which mediates H3K27 trimethylation. This blocks Wnt gene expression, inducing the upregulation of PPARgamma and Cebpa and driving increased adipogenesis. Consistent with this finding, white adipose tissue from S6K1-deficient mice exhibits no detectable H2BS36 phosphorylation or H3K27 trimethylation, whereas both responses are highly elevated in obese humans or in mice fed a high-fat diet. These findings define an S6K1-dependent mechanism in early adipogenesis, contributing to the promotion of obesity. |
