E3 Ubiquitin Ligases in Gammaherpesviruses and HIV: A Review of Virus Adaptation and Exploitation.

E3 Ubiquitin Ligases in Gammaherpesviruses and HIV: A Review of Virus Adaptation and Exploitation.
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DOI:
10.3390/v15091935
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发表时间:
2023-09-15
期刊:
Viruses
影响因子:
--
通讯作者:
Ehrlich ES
Ehrlich ES
中科院分区:
其他
文献类型:
--
作者:
Oswald J;Constantine M;Adegbuyi A;Omorogbe E;Dellomo AJ;Ehrlich ES

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为了产生感染和复制,病毒必须控制细胞机制并抵消限制因子和抗病毒蛋白。病毒可以通过调控细胞基因表达以及转录后和翻译后控制来实现这一点。许多病毒通过调节宿主翻译后修饰机制、编码或劫持激酶、SUMO连接酶、去泛素酶和泛素连接酶以及其他修饰剂来协同和抵消细胞过程。本文综述了三种癌病毒,eb病毒(EBV)、卡波西肉瘤疱疹病毒(KSHV)和人类免疫缺陷病毒(HIV),以及它们通过病毒编码或细胞E3泛素连接酶活性与泛素-蛋白酶体系统的相互作用。
For productive infection and replication to occur, viruses must control cellular machinery and counteract restriction factors and antiviral proteins. Viruses can accomplish this, in part, via the regulation of cellular gene expression and post-transcriptional and post-translational control. Many viruses co-opt and counteract cellular processes via modulation of the host post-translational modification machinery and encoding or hijacking kinases, SUMO ligases, deubiquitinases, and ubiquitin ligases, in addition to other modifiers. In this review, we focus on three oncoviruses, Epstein–Barr virus (EBV), Kaposi’s sarcoma herpesvirus (KSHV), and human immunodeficiency virus (HIV) and their interactions with the ubiquitin–proteasome system via viral-encoded or cellular E3 ubiquitin ligase activity.
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