Oncogenic steroid receptor coactivator-3 is a key regulator of the white adipogenic program.

The white adipocyte is at the center of dysfunctional regulatory pathways in various pathophysiological processes, including obesity, diabetes, inflammation, and cancer. Here, we show that the oncogenic steroid receptor coactivator-3 (SRC-3) is a critical regulator of white adipocyte development. Indeed, in SRC-3(-/-) mouse embryonic fibroblasts, adipocyte differentiation was severely impaired, ...
and reexpression of SRC-3 was able to restore it. The early stages of adipocyte differentiation are accompanied by an increase in nuclear levels of SRC-3, which accumulates to high levels specifically in the nucleus of differentiated fat cells. Moreover, SRC-3(-/-) animals showed reduced body weight and adipose tissue mass with a significant decrease of the expression of peroxisome proliferator-activated receptor gamma2 (PPARgamma2), a master gene required for adipogenesis. At the molecular level, SRC-3 acts synergistically with the transcription factor CAAT/enhancer-binding protein to control the gene expression of PPARgamma2. Collectively, these data suggest a crucial role for SRC-3 as an integrator of the complex transcriptional network controlling adipogenesis.
Mesh Terms:
3T3 Cells, Adipocytes, White, Animals, Body Weight, CCAAT-Enhancer-Binding Proteins, Cell Differentiation, Fibroblasts, Gene Expression Regulation, Developmental, HeLa Cells, Histone Acetyltransferases, Humans, Male, Mice, Mice, Inbred C57BL, Mice, Knockout, Nuclear Receptor Coactivator 3, PPAR gamma, Promoter Regions, Genetic, Trans-Activators, Transcription, Genetic
Proc. Natl. Acad. Sci. U.S.A.
Date: Nov. 21, 2006
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