Pennington Biomedical Research Center, Louisiana State University System, Baton Rouge, Louisiana, USA.
Obesity (Silver Spring). 2021 Jan;29(1):98-107. doi: 10.1002/oby.23013. Epub 2020 Nov 6.
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.
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.
Siah2 is expressed in platelet-derived growth factor receptor α (PDGFRα) 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.
Siah2 is expressed in PDGFRα+ 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.
锌指蛋白 423(ZFP423)是脂肪细胞前体细胞中关键的促脂肪生成转录因子,其表达受促脂肪生成早期 B 细胞因子 1(EBF1)和抗脂肪生成 ZFP521 的相互作用调节。泛素连接酶七缺失同源物 2(SIAH2)将 ZFP521 作为靶标进行降解。本研究探讨了 SIAH2 是否在脂肪细胞前体细胞中表达,以及 SIAH2 是否与 ZFP521 和 EBF1 相互作用,以在脂肪生成过程中调节 ZFP521 蛋白水平。
在接受对照或高脂肪饮食喂养的野生型和 SIAH2 基因敲除小鼠的原代细胞和组织中评估前体细胞中的 SIAH2 表达。使用原代细胞、3T3-L1 前脂肪细胞和 HEK293T 细胞分析 Siah2、Ebf1 和 Zfp521 的表达以及 SIAH2 介导的 ZFP521 和 EBF1 蛋白水平的变化。
Siah2 在血小板衍生生长因子受体α(PDGFRα)和干细胞抗原-1(SCA1)脂肪细胞前体细胞中表达。SIAH2 耗竭减少 Ebf1 基因表达,并增加早期而非晚期脂肪生成中的 EBF1 蛋白水平。在早期脂肪生成中,SIAH2 与 EBF1 和 ZFP521 形成蛋白质复合物,增强 SIAH2 介导的 ZFP521 泛素化和降解,同时增加 EBF1 蛋白水平。
Siah2 在 PDGFRα+脂肪细胞前体细胞中表达,并通过与 EBF1 和 ZFP521 蛋白相互作用,与前体细胞向脂肪生成的定向作用相关,以将抗脂肪生成的 ZFP521 作为靶标进行降解。