Year: 2016
Type: article
Abstract: Adipogenesis is orchestrated by a highly ordered network of transcription factors including peroxisome-proliferator activated receptor-gamma (PPARγ) and CCAAT-enhancer binding protein (C/EBP) family proteins. High mobility group protein AT-hook 2 (HMGA2), an architectural transcription factor, has been reported to play an essential role in preadipocyte proliferation, and its overexpression has been implicated in obesity in mice and humans. However, the direct role of HMGA2 in regulating the gene expression program during adipogenesis is not known. Here, we demonstrate that HMGA2 is required for C/EBPβ-mediated expression of PPARγ, and thus promotes adipogenic differentiation. We observed a transient but marked increase of Hmga2 transcript at an early phase of differentiation of mouse 3T3-L1 preadipocytes. Importantly, Hmga2 knockdown greatly impaired adipocyte formation, while its overexpression promoted the formation of mature adipocytes. We found that HMGA2 colocalized with C/EBPβ in the nucleus and was required for the recruitment of C/EBPβ to its binding element at the Pparγ2 promoter. Accordingly, HMGA2 and C/EBPβ cooperatively enhanced the Pparγ2 promoter activity. Our results indicate that HMGA2 is an essential constituent of the adipogenic transcription factor network, and thus its function may be affected during the course of obesity.
Language: English
Subfield: Molecular Biology
Domain: Life Sciences
Open Access status: hybrid
Estimated APC paid: $3,110
Funders: Takeda Science Foundation, Nakatomi Foundation, Japan Agency for Medical Research and Development, Ministry of Education, Culture, Sports, Science and Technology, National Natural Science Foundation of China, Ningbo University, Natural Science Foundation of Ningbo, Japan Society for the Promotion of Science, K. C. Wong Magna Fund in Ningbo University, Core Research for Evolutional Science and Technology
Awards: G2599811567, Molecular mechanisms of a functional linkage between epigenome and mitochondria, and its pathophysiological association, G3181274460, Study on the epigenetic regulation of metabolic programming and energy homeostasis, G6497730220, G7423070718, Functional analysis of epigenetic factors that inhibit cellular senescence, LincRNA-p21对PTEN乙酰化修饰在抗肺纤维化中的作用和机制
OpenAlex ID: W2302445780
