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Wwp2,一种将转录因子Oct-4作为泛素化靶点的E3泛素连接酶。

Wwp2, an E3 ubiquitin ligase that targets transcription factor Oct-4 for ubiquitination.

作者信息

Xu Hui Ming, Liao Bing, Zhang Qian Jun, Wang Bei Bei, Li Hui, Zhong Xiao Min, Sheng Hui Zhen, Zhao Ying Xin, Zhao Ying Ming, Jin Ying

机构信息

Developmental Biology Department, Health Science Center, Shanghai Second Medical University and Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, 411 He Fei Road, Shanghai 200025, China.

出版信息

J Biol Chem. 2004 May 28;279(22):23495-503. doi: 10.1074/jbc.M400516200. Epub 2004 Mar 26.

Abstract

The POU transcription factor Oct-4 is a master regulator affecting the fate of pluripotent embryonic stem cells. However, the precise mechanisms by which the activation and expression of Oct-4 are regulated still remain to be elucidated. We describe here a novel murine ubiquitin ligase, Wwp2, that specifically interacts with Oct-4 and promotes its ubiquitination both in vivo and in vitro. Remarkably, the expression of a catalytically inactive point mutant of Wwp2 abolishes Oct-4 ubiquitination. Moreover, Wwp2 promotes Oct-4 degradation in the presence of overexpressed ubiquitin. The degradation is blocked by treatment with proteasome inhibitor. Fusion of a single ubiquitin to Oct-4 inactivates its transcriptional activity in a heterologous Oct-4-driven reporter system. Furthermore, overexpression of Wwp2 in embryonic stem cells significantly reduces the Oct-4-transcriptional activities. Collectively, we demonstrate for the first time that Oct-4 can be post-translationally modified by ubiquitination and that this modification dramatically suppresses its transcriptional activity. These results reveal that the functional status of Oct-4, in addition to its expression level, dictates its transcriptional activity, and the results open up a new avenue to understand how Oct-4 defines the fate of embryonic stem cells.

摘要

POU转录因子Oct-4是影响多能胚胎干细胞命运的主要调节因子。然而,Oct-4激活和表达的精确调控机制仍有待阐明。我们在此描述一种新型小鼠泛素连接酶Wwp2,它在体内和体外均能特异性地与Oct-4相互作用并促进其泛素化。值得注意的是,Wwp2催化失活点突变体的表达消除了Oct-4的泛素化。此外,在过表达泛素的情况下,Wwp2促进Oct-4降解。蛋白酶体抑制剂处理可阻断这种降解。在异源Oct-4驱动的报告系统中,将单个泛素与Oct-4融合会使其转录活性失活。此外,在胚胎干细胞中过表达Wwp2会显著降低Oct-4的转录活性。总体而言,我们首次证明Oct-4可通过泛素化进行翻译后修饰,且这种修饰会显著抑制其转录活性。这些结果表明,Oct-4的功能状态除了其表达水平外,还决定其转录活性,并且这些结果为理解Oct-4如何决定胚胎干细胞的命运开辟了一条新途径。

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