| First Author | Park JH | Year | 2013 |
| Journal | Dev Cell | Volume | 26 |
| Issue | 4 | Pages | 393-404 |
| PubMed ID | 23987512 | Mgi Jnum | J:204551 |
| Mgi Id | MGI:5532794 | Doi | 10.1016/j.devcel.2013.07.002 |
| Citation | Park JH, et al. (2013) A multifunctional protein, EWS, is essential for early brown fat lineage determination. Dev Cell 26(4):393-404 |
| abstractText | The recent surge in obesity has provided an impetus to better understand the mechanisms of adipogenesis, particularly in brown adipose tissue (BAT) because of its potential utilization for antiobesity therapy. Postnatal brown adipocytes arise from early muscle progenitors, but how brown fat lineage is determined is not completely understood. Here, we show that a multifunctional protein, Ewing Sarcoma (EWS), is essential for determining brown fat lineage during development. BATs from Ews null embryos and newborns are developmentally arrested. Ews mutant brown preadipocytes fail to differentiate due to loss of Bmp7 expression, a critical early brown adipogenic factor. We demonstrate that EWS, along with its binding partner Y-box binding protein 1 (YBX1), activates Bmp7 transcription. Depletion of either Ews or Ybx1 leads to loss of Bmp7 expression and brown adipogenesis. Remarkably, Ews null BATs and brown preadipocytes ectopically express myogenic genes. These results demonstrate that EWS is essential for early brown fat lineage determination. |
