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本文引用的文献

1
Early adipogenesis is regulated through USP7-mediated deubiquitination of the histone acetyltransferase TIP60.早期脂肪生成受 USP7 介导的组蛋白乙酰转移酶 TIP60 的去泛素化调控。
Nat Commun. 2013;4:2656. doi: 10.1038/ncomms3656.
2
Deubiquitination of Tip60 by USP7 determines the activity of the p53-dependent apoptotic pathway.USP7 通过去泛素化 Tip60 来决定 p53 依赖性凋亡途径的活性。
Mol Cell Biol. 2013 Aug;33(16):3309-20. doi: 10.1128/MCB.00358-13. Epub 2013 Jun 17.
3
Dynamic and distinct histone modifications modulate the expression of key adipogenesis regulatory genes.动态且独特的组蛋白修饰调节关键脂肪生成调节基因的表达。
Cell Cycle. 2012 Dec 1;11(23):4310-22. doi: 10.4161/cc.22224. Epub 2012 Oct 19.
4
A novel RNAi lethality rescue screen to identify regulators of adipogenesis.一种用于鉴定脂肪生成调节因子的新型RNA干扰致死性拯救筛选。
PLoS One. 2012;7(6):e37680. doi: 10.1371/journal.pone.0037680. Epub 2012 Jun 5.
5
The ubiquitin system, an immense realm.泛素系统,一个庞大的领域。
Annu Rev Biochem. 2012;81:167-76. doi: 10.1146/annurev-biochem-051910-094049.
6
The ubiquitin ligase Siah2 regulates PPARγ activity in adipocytes.泛素连接酶 Siah2 调节脂肪细胞中 PPARγ 的活性。
Endocrinology. 2012 Mar;153(3):1206-18. doi: 10.1210/en.2011-1725. Epub 2012 Jan 31.
7
Forming functional fat: a growing understanding of adipocyte differentiation.形成功能性脂肪:对脂肪细胞分化的日益深入了解。
Nat Rev Mol Cell Biol. 2011 Sep 28;12(11):722-34. doi: 10.1038/nrm3198.
8
Proteasome alterations during adipose differentiation and aging: links to impaired adipocyte differentiation and development of oxidative stress.蛋白酶体在脂肪分化和衰老过程中的改变:与脂肪细胞分化受损和氧化应激发展的关联。
Free Radic Biol Med. 2011 Nov 1;51(9):1727-35. doi: 10.1016/j.freeradbiomed.2011.08.001. Epub 2011 Aug 10.
9
Regulation of cell fate determination by Skp1-Cullin1-F-box (SCF) E3 ubiquitin ligases.Skp1-Cullin1-F-box(SCF)E3泛素连接酶对细胞命运决定的调控。
Int J Dev Biol. 2011;55(3):249-60. doi: 10.1387/ijdb.103171ch.
10
NCoR1 regulates thyroid hormone receptor isoform-dependent adipogenesis.NCoR1 调节甲状腺激素受体异构体依赖性脂肪生成。
J Mol Endocrinol. 2011 Jun 9;46(3):233-44. doi: 10.1530/JME-10-0163. Print 2011 Jun.

tipped 脂肪生成中的平衡:USP7 介导的 Tip60 稳定。

TIPping the balance in adipogenesis: USP7-mediated stabilization of Tip60.

机构信息

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.

出版信息

Adipocyte. 2014 Apr 1;3(2):160-5. doi: 10.4161/adip.28307. Epub 2014 Feb 25.

DOI:10.4161/adip.28307
PMID:24719792
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3979883/
Abstract

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.

摘要

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。