1. Academic Validation
  2. Transcriptional regulation of adipocyte differentiation: a central role for CCAAT/enhancer-binding protein (C/EBP) β

Transcriptional regulation of adipocyte differentiation: a central role for CCAAT/enhancer-binding protein (C/EBP) β

  • J Biol Chem. 2015 Jan 9;290(2):755-61. doi: 10.1074/jbc.R114.619957.
Liang Guo 1 Xi Li 1 Qi-Qun Tang 2
Affiliations

Affiliations

  • 1 From the Key Laboratory of Metabolism and Molecular Medicine, the Ministry of Education and Department of Biochemistry and Molecular Biology, Fudan University Shanghai Medical College, Shanghai 200032, China.
  • 2 From the Key Laboratory of Metabolism and Molecular Medicine, the Ministry of Education and Department of Biochemistry and Molecular Biology, Fudan University Shanghai Medical College, Shanghai 200032, China [email protected].
Abstract

A detailed understanding of the processes controlling adipogenesis is instrumental in the fight against the obesity epidemic. Adipogenesis is controlled by a transcriptional cascade composed of a large number of transcriptional factors, among which CCAAT/enhancer-binding protein (C/EBP) β plays an essential role. During 3T3-L1 adipocyte differentiation, C/EBPβ is induced early to transactivate the expression of C/EBPα and Peroxisome Proliferator-activated Receptor γ (PPARγ), two master transcription factors for terminal adipocyte differentiation. Studies in recent years have revealed many new target genes of C/EBPβ, implicating its participation in many other processes during adipogenesis, such as mitotic clonal expansion, epigenetic regulation, unfolded protein response, and Autophagy. Moreover, the function of C/EBPβ is highly regulated by post-translational modifications, which are crucial for the proper activation of the adipogenic program. Advances toward elucidation of the function and roles of the post-translational modification of C/EBPβ during adipogenesis will greatly improve our understanding of the molecular mechanisms governing adipogenesis.

Keywords

Autophagy; CCAAT-Enhancer-binding Protein (C/EBP); Cell Proliferation; Epigenetics; Post-translational Modification (PTM); Unfolded Protein Response (UPR); adipogenesis.

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