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The Epstein-Barr virus miR-BHRF1-1 targets RNF4 during productive infection to promote the accumulation of SUMO conjugates and the release of infectious virus.爱泼斯坦-巴尔病毒的miR-BHRF1-1在增殖性感染期间靶向RNF4,以促进SUMO缀合物的积累和传染性病毒的释放。
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本文引用的文献

1
Sumo paralogs: redundancy and divergencies.相扑旁系同源物:冗余与差异
Front Biosci (Schol Ed). 2013 Jan 1;5(2):544-53. doi: 10.2741/s388.
2
The human cytomegalovirus DNA polymerase processivity factor UL44 is modified by SUMO in a DNA-dependent manner.人巨细胞病毒 DNA 聚合酶延伸因子 UL44 以依赖 DNA 的方式被 SUMO 修饰。
PLoS One. 2012;7(11):e49630. doi: 10.1371/journal.pone.0049630. Epub 2012 Nov 15.
3
Cross-talk between phosphorylation and SUMOylation regulates transforming activities of an adenoviral oncoprotein.磷酸化和 SUMO 化之间的串扰调节腺病毒癌蛋白的转化活性。
Oncogene. 2013 Mar 28;32(13):1626-37. doi: 10.1038/onc.2012.187. Epub 2012 May 21.
4
The RanBP2/RanGAP1*SUMO1/Ubc9 complex is a multisubunit SUMO E3 ligase.RanBP2/RanGAP1*SUMO1/Ubc9 复合物是一种多亚基 SUMO E3 连接酶。
Mol Cell. 2012 May 11;46(3):287-98. doi: 10.1016/j.molcel.2012.02.017. Epub 2012 Mar 29.
5
Induction of type I IFNs by intracellular DNA-sensing pathways.细胞内 DNA 感应途径诱导 I 型干扰素。
Immunol Cell Biol. 2012 May;90(5):474-82. doi: 10.1038/icb.2012.11. Epub 2012 Mar 27.
6
SUMO binding by the Epstein-Barr virus protein kinase BGLF4 is crucial for BGLF4 function.SUMO 结合由 Epstein-Barr 病毒蛋白激酶 BGLF4 介导,对 BGLF4 功能至关重要。
J Virol. 2012 May;86(10):5412-21. doi: 10.1128/JVI.00314-12. Epub 2012 Mar 7.
7
DeSUMOylating isopeptidase: a second class of SUMO protease.去 SUMO 化异构酶:第二类 SUMO 蛋白酶。
EMBO Rep. 2012 Apr;13(4):339-46. doi: 10.1038/embor.2012.3.
8
Post-Translational Modifications of Kaposi's Sarcoma-Associated Herpesvirus Regulatory Proteins - SUMO and KSHV.卡波西肉瘤相关疱疹病毒调节蛋白的翻译后修饰——小泛素样修饰蛋白与卡波西肉瘤相关疱疹病毒
Front Microbiol. 2012 Feb 14;3:31. doi: 10.3389/fmicb.2012.00031. eCollection 2012.
9
Regulation of vaccinia virus E3 protein by small ubiquitin-like modifier proteins.小泛素样修饰蛋白对牛痘病毒 E3 蛋白的调节。
J Virol. 2011 Dec;85(24):12890-900. doi: 10.1128/JVI.05628-11. Epub 2011 Sep 28.
10
A viral ubiquitin ligase has substrate preferential SUMO targeted ubiquitin ligase activity that counteracts intrinsic antiviral defence.一种病毒泛素连接酶具有底物偏好性 SUMO 靶向泛素连接酶活性,可对抗固有抗病毒防御。
PLoS Pathog. 2011 Sep;7(9):e1002245. doi: 10.1371/journal.ppat.1002245. Epub 2011 Sep 15.

病毒对细胞蛋白质缀合途径的操控:小泛素样修饰蛋白的启示

Viral manipulation of cellular protein conjugation pathways: The SUMO lesson.

作者信息

Mattoscio Domenico, Segré Chiara V, Chiocca Susanna

机构信息

Domenico Mattoscio, Chiara V Segré, Susanna Chiocca, Department of Experimental Oncology, European Institute of Oncology, Via Adamello 16, 20139 Milan, Italy.

出版信息

World J Virol. 2013 May 12;2(2):79-90. doi: 10.5501/wjv.v2.i2.79.

DOI:10.5501/wjv.v2.i2.79
PMID:24175232
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3785051/
Abstract

Small ubiquitin-like modifier (SUMO)ylation is a key post-translational modification mechanism that controls the function of a plethora of proteins and biological processes. Given its central regulatory role, it is not surprising that it is widely exploited by viruses. A number of viral proteins are known to modify and/or be modified by the SUMOylation system to exert their function, to create a cellular environment more favorable for virus survival and propagation, and to prevent host antiviral responses. Since the SUMO pathway is a multi-step cascade, viral proteins engage with it at many levels, to advance and favor each stage of a typical infection cycle: replication, viral assembly and immune evasion. Here we review the current knowledge on the interplay between the host SUMO system and viral lifecycle.

摘要

小泛素样修饰物(SUMO)化是一种关键的翻译后修饰机制,可控制众多蛋白质的功能及生物过程。鉴于其核心调控作用,病毒广泛利用这一机制也就不足为奇了。已知许多病毒蛋白会被SUMO化系统修饰和/或对该系统进行修饰,以发挥其功能、营造更有利于病毒存活和传播的细胞环境,并阻止宿主的抗病毒反应。由于SUMO途径是一个多步骤级联反应,病毒蛋白在多个层面与之相互作用,以推进并促进典型感染周期的各个阶段:复制、病毒组装和免疫逃逸。在此,我们综述了关于宿主SUMO系统与病毒生命周期之间相互作用的现有知识。