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人类1型T细胞白血病病毒Tax癌蛋白激活核因子-κB需要泛素结合酶Ubc13。

The human T-cell leukemia virus type 1 Tax oncoprotein requires the ubiquitin-conjugating enzyme Ubc13 for NF-kappaB activation.

作者信息

Shembade Noula, Harhaj Nicole S, Yamamoto Masahiro, Akira Shizuo, Harhaj Edward W

机构信息

Department of Microbiology and Immunology, Sylvester Comprehensive Cancer Center, the University of Miami, Miller School of Medicine, 1550 NW 10 Avenue, Miami, FL 33136, USA.

出版信息

J Virol. 2007 Dec;81(24):13735-42. doi: 10.1128/JVI.01790-07. Epub 2007 Oct 17.

Abstract

Ubiquitination of the human T-cell leukemia virus 1 Tax oncoprotein provides an important regulatory mechanism that promotes the Tax-mediated activation of NF-kappaB. However, the type of polyubiquitin chain linkages and the host factors that are required for Tax ubiquitination have not been identified. Here, we demonstrate that Tax polyubiquitin chains are composed predominantly of lysine 63-linked chains. Furthermore, the ubiquitination of Tax is critically dependent on the E2 ubiquitin-conjugating enzyme Ubc13. Tax interacts with Ubc13, and small interfering RNA-mediated knockdown of Ubc13 expression abrogates Tax ubiquitination and the activation of NF-kappaB. Mouse fibroblasts lacking Ubc13 exhibit impaired Tax activation of NF-kappaB despite normal tumor necrosis factor- and interleukin-1-mediated NF-kappaB activation. Finally, the interaction of Tax with NEMO is disrupted in the absence of Tax ubiquitination and Ubc13 expression, suggesting that Tax ubiquitination is critical for NEMO binding. Collectively, our results reveal that Ubc13 is essential for Tax ubiquitination, its interaction with NEMO, and Tax-mediated NF-kappaB activation.

摘要

人类T细胞白血病病毒1型Tax癌蛋白的泛素化提供了一种重要的调节机制,可促进Tax介导的核因子-κB激活。然而,尚未确定Tax泛素化所需的多聚泛素链连接类型和宿主因子。在此,我们证明Tax多聚泛素链主要由赖氨酸63连接的链组成。此外,Tax的泛素化严重依赖于E2泛素结合酶Ubc13。Tax与Ubc13相互作用,小干扰RNA介导的Ubc13表达敲低消除了Tax泛素化和核因子-κB激活。缺乏Ubc13的小鼠成纤维细胞尽管肿瘤坏死因子和白细胞介素-1介导的核因子-κB激活正常,但Tax激活核因子-κB的能力受损。最后,在缺乏Tax泛素化和Ubc13表达的情况下,Tax与NEMO的相互作用被破坏,这表明Tax泛素化对NEMO结合至关重要。总之,我们的结果表明,Ubc13对于Tax泛素化、其与NEMO的相互作用以及Tax介导的核因子-κB激活至关重要。

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