Molecular Cancer Research; Center for Molecular Medicine; University Medical Centre Utrecht; Utrecht, The Netherlands ; Department of Biochemistry and Molecular Biology; School of Medicine; Soochow University; Suzhou, PR China.
Molecular Cancer Research; Center for Molecular Medicine; University Medical Centre Utrecht; Utrecht, The Netherlands.
Adipocyte. 2014 Apr 1;3(2):160-5. doi: 10.4161/adip.28307. Epub 2014 Feb 25.
Adipogenesis is regulated by a complex interplay between transcription factors, in concert with-among others-transcriptional cofactors, signaling cascades and miRNAs. Several studies have implicated the transcriptional cofactor and acetyltransferase Tip60 in PPARγ signaling and adipocyte differentiation. Since Tip60 protein levels, but not mRNA levels, are upregulated during adipogenesis, and since Tip60 can be degraded by the proteasome, we hypothesized that Tip60 protein may be stabilized through deubiquitination during adipogenesis. Indeed, Tip60 is protected from proteasomal degeradation by the deubiquitinase USP7, which is particularly important for mitotic clonal expansion (MCE), an early step in adipogenesis. Besides this novel role in early differentiation, earlier studies indicated that Tip60 is also important during the later stages of differentiation, indicating a dual role for this protein in adipogenesis. Our recent study sheds new light on the role of Tip60 in cellular differentiation and provide new insights into the importance of a regulatory process that has not been studied intensively in adipogenesis: protein (de)ubiquitination.
脂肪生成受转录因子之间的复杂相互作用调节,与转录共因子、信号级联和 miRNA 一起。几项研究表明,转录共因子和乙酰转移酶 Tip60 参与了 PPARγ 信号和脂肪细胞分化。由于 Tip60 蛋白水平而不是 mRNA 水平在脂肪生成过程中上调,并且由于 Tip60 可以被蛋白酶体降解,因此我们假设 Tip60 蛋白可能在脂肪生成过程中通过去泛素化而稳定。事实上,去泛素酶 USP7 保护 Tip60 免受蛋白酶体降解,这对有丝分裂克隆扩增(MCE)特别重要,MCE 是脂肪生成的早期步骤。除了在早期分化中的这个新作用外,早期研究表明 Tip60 在分化的后期阶段也很重要,这表明该蛋白在脂肪生成中具有双重作用。我们最近的研究揭示了 Tip60 在细胞分化中的作用,并为尚未在脂肪生成中深入研究的调控过程的重要性提供了新的见解:蛋白质(去)泛素化。