期刊
OBESITY
卷 29, 期 1, 页码 98-107出版社
WILEY
DOI: 10.1002/oby.23013
关键词
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资金
- National Institutes of Health (NIDDK) [1R01 DK099625]
- Center of Biological Research Excellence (COBRE) [NIH8 P30GM118430-01]
- Nutrition Obesity Research Center (NORC) [NIH P30 DK072476]
- John S. McIlhenny Endowed Postdoctoral Fellowship
SIAH2 is expressed in adipocyte precursor cells and interacts with EBF1 and ZFP521 to enhance the degradation of ZFP521 while increasing EBF1 levels, revealing its role in regulating adipogenesis.
Objective Expression of zinc finger protein 423 (ZFP423), a key proadipogenic transcription factor in adipocyte precursor cells, is regulated by interaction of the proadipogenic early B-cell factor 1 (EBF1) and antiadipogenic ZFP521. The ubiquitin ligase seven-in-absentia homolog 2 (SIAH2) targets ZFP521 for degradation. This study asked whether SIAH2 is expressed in adipocyte precursor cells and whether SIAH2 interacts with ZFP521 and EBF1 to regulate ZFP521 protein levels during adipogenesis. Methods SIAH2 expression in precursor cells was assessed in primary cells and tissues from wild-type and SIAH2 null mice fed a control or high-fat diet. Primary cells, 3T3-L1 preadipocytes, and HEK293T cells were used to analyze Siah2, Ebf1, and Zfp521 expression and SIAH2-mediated changes in ZFP521 and EBF1 protein levels. Results Siah2 is expressed in platelet-derived growth factor receptor alpha (PDGFR alpha)(+) and stem cell antigen-1 (SCA1)(+) adipocyte precursor cells. SIAH2 depletion reduces Ebf1 gene expression and increases EBF1 protein levels in early but not late adipogenesis. In early adipogenesis, SIAH2 forms a protein complex with EBF1 and ZFP521 to enhance SIAH2-mediated ubiquitylation and degradation of ZFP521 while increasing EBF1 protein levels. Conclusions Siah2 is expressed in PDGFR alpha+ adipocyte precursor cells and is linked to precursor cell commitment to adipogenesis by interacting with EBF1 and ZFP521 proteins to target the antiadipogenic ZFP521 for degradation.
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