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在脂肪生成过程中,被激活的 STAT1 的蛋白抑制剂(PIAS1)被鉴定为 CCAAT/增强子结合蛋白β(C/EBPβ)的 SUMO E3 连接酶。

Protein inhibitor of activated STAT 1 (PIAS1) is identified as the SUMO E3 ligase of CCAAT/enhancer-binding protein β (C/EBPβ) during adipogenesis.

机构信息

Key Laboratory of Molecular Medicine, Ministry of Education, and Department of Biochemistry and Molecular Biology, Fudan University Shanghai Medical College, Shanghai, People's Republic of China.

出版信息

Mol Cell Biol. 2013 Nov;33(22):4606-17. doi: 10.1128/MCB.00723-13. Epub 2013 Sep 23.

Abstract

It is well recognized that PIAS1, a SUMO (small ubiquitin-like modifier) E3 ligase, modulates such cellular processes as cell proliferation, DNA damage responses, and inflammation responses. Recent studies have shown that PIAS1 also plays a part in cell differentiation. However, the role of PIAS1 in adipocyte differentiation remains unknown. CCAAT/enhancer-binding protein β (C/EBPβ), a major regulator of adipogenesis, is a target of SUMOylation, but the E3 ligase responsible for the SUMOylation of C/EBPβ has not been identified. The present study showed that PIAS1 functions as a SUMO E3 ligase of C/EBPβ to regulate adipogenesis. PIAS1 expression was significantly and transiently induced on day 4 of 3T3-L1 adipocyte differentiation, when C/EBPβ began to decline. PIAS1 was found to interact with C/EBPβ through the SAP (scaffold attachment factor A/B/acinus/PIAS) domain and SUMOylate it, leading to increased ubiquitination and degradation of C/EBPβ. C/EBPβ became more stable when PIAS1 was silenced by RNA interference (RNAi). Moreover, adipogenesis was inhibited by overexpression of wild-type PIAS1 and promoted by knockdown of PIAS1. The mutational study indicated that the catalytic activity of SUMO E3 ligase was required for PIAS1 to restrain adipogenesis. Importantly, the inhibitory effect of PIAS1 overexpression on adipogenesis was rescued by overexpressed C/EBPβ. Thus, PIAS1 could play a dynamic role in adipogenesis by promoting the SUMOylation of C/EBPβ.

摘要

众所周知,PIAS1 是一种 SUMO(小泛素样修饰物)E3 连接酶,可调节细胞增殖、DNA 损伤反应和炎症反应等细胞过程。最近的研究表明,PIAS1 也参与细胞分化。然而,PIAS1 在脂肪细胞分化中的作用尚不清楚。CCAAT/增强子结合蛋白β(C/EBPβ)是脂肪生成的主要调节因子,是 SUMOylation 的靶标,但负责 C/EBPβ SUMOylation 的 E3 连接酶尚未确定。本研究表明,PIAS1 作为 C/EBPβ 的 SUMO E3 连接酶发挥作用,调节脂肪生成。在 3T3-L1 脂肪细胞分化的第 4 天,当 C/EBPβ 开始下降时,PIAS1 的表达明显且短暂地被诱导。发现 PIAS1 通过 SAP(支架附着因子 A/B/acinus/PIAS)结构域与 C/EBPβ 相互作用,并对其进行 SUMOylation,导致 C/EBPβ 的泛素化和降解增加。当 PIAS1 通过 RNA 干扰(RNAi)沉默时,C/EBPβ 变得更加稳定。此外,过表达野生型 PIAS1 抑制脂肪生成,而敲低 PIAS1 则促进脂肪生成。突变研究表明,SUMO E3 连接酶的催化活性对于 PIAS1 抑制脂肪生成是必需的。重要的是,PIAS1 过表达对脂肪生成的抑制作用可以通过过表达的 C/EBPβ 得到挽救。因此,PIAS1 可以通过促进 C/EBPβ 的 SUMOylation 在脂肪生成中发挥动态作用。

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