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Cell Death Differ. 2012 Aug;19(8):1381-9. doi: 10.1038/cdd.2012.15. Epub 2012 Mar 2.

Mdm2 controls CREB-dependent transactivation and initiation of adipocyte differentiation.

Author information

1
Department of Biochemistry and Molecular Biology, University of Southern Denmark, Odense, Denmark.

Abstract

The role of the E3 ubiquitin ligase murine double minute 2 (Mdm2) in regulating the stability of the p53 tumor suppressor is well documented. By contrast, relatively little is known about p53-independent activities of Mdm2 and the role of Mdm2 in cellular differentiation. Here we report a novel role for Mdm2 in the initiation of adipocyte differentiation that is independent of its ability to regulate p53. We show that Mdm2 is required for cAMP-mediated induction of CCAAT/enhancer-binding protein δ (C/EBPδ) expression by facilitating recruitment of the cAMP regulatory element-binding protein (CREB) coactivator, CREB-regulated transcription coactivator (Crtc2)/TORC2, to the c/ebpδ promoter. Our findings reveal an unexpected role for Mdm2 in the regulation of CREB-dependent transactivation during the initiation of adipogenesis. As Mdm2 is able to promote adipogenesis in the myoblast cell line C2C12, it is conceivable that Mdm2 acts as a switch in cell fate determination.

PMID:
22388350
PMCID:
PMC3392627
DOI:
10.1038/cdd.2012.15
[Indexed for MEDLINE]
Free PMC Article

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