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


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 ? (C/EBP?) expression by facilitating recruitment of the cAMP regulatory element-binding protein (CREB) coactivator, CREB-regulated transcription coactivator (Crtc2)/TORC2, to the c/ebp? 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.

SUBMITTER: Hallenborg P 

PROVIDER: S-EPMC3392627 | biostudies-literature | 2012 Aug

REPOSITORIES: biostudies-literature

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

Hallenborg P P   Feddersen S S   Francoz S S   Murano I I   Sundekilde U U   Petersen R K RK   Akimov V V   Olson M V MV   Lozano G G   Cinti S S   Gjertsen B T BT   Madsen L L   Marine J-C JC   Blagoev B B   Kristiansen K K  

Cell death and differentiation 20120302 8


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  ...[more]

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