Oswald Jessica, Constantine Mathew, Adegbuyi Adedolapo, Omorogbe Esosa, Dellomo Anna J, Ehrlich Elana S
Department of Biological Sciences, Towson University, Towson, MD 21252, USA.
Viruses. 2023 Sep 15;15(9):1935. doi: 10.3390/v15091935.
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.
为了实现有效的感染和复制,病毒必须控制细胞机制,并对抗限制因子和抗病毒蛋白。病毒可以部分通过调节细胞基因表达以及转录后和翻译后控制来做到这一点。除了其他修饰因子外,许多病毒还通过调节宿主翻译后修饰机制以及编码或劫持激酶、SUMO连接酶、去泛素酶和泛素连接酶来利用和对抗细胞过程。在本综述中,我们重点关注三种致癌病毒,即爱泼斯坦-巴尔病毒(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。