Post-translational modifications on protein VII are important during the early stages of adenovirus infection.

IF 3.8 2区 医学 Q2 VIROLOGY Journal of Virology Pub Date : 2025-02-25 Epub Date: 2024-12-31 DOI:10.1128/jvi.01462-24
Edward A Arnold, Julian R Smith, Katie Leung, Daniel H Nguyen, Laurel E Kelnhofer-Millevolte, Monica S Guo, Jason G Smith, Daphne C Avgousti
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Abstract

Due to the importance of post-translational modification (PTM) in cellular function, viruses have evolved to both take advantage of and be susceptible to such modification. Adenovirus encodes a multifunctional protein called protein VII, which is packaged with the viral genome in the core of virions and disrupts host chromatin during infection. Protein VII has several PTMs whose addition contributes to the subnuclear localization of protein VII. Here, we used mutant viruses that abrogate or mimic these PTMs on protein VII to interrogate their impact on protein VII function during adenovirus infection. We discovered that acetylation of the lysine in positions 2 or 3 (K2 or K3) is deleterious during early infection as mutation to alanine led to greater intake of protein VII and viral DNA to the nucleus and enhanced early gene expression. Furthermore, we determined that protein VII is acetylated at alternative residues late during infection which may compensate for the mutated sites. Lastly, due to the role of the early viral protein E1A in viral gene activation, we investigated the interaction between protein VII and E1A and demonstrated that protein VII interacts with E1A through a chromatin-mediated interaction. Together, these results emphasize that the complexity of virus-host interactions is intimately tied to post-translational modification.

Importance: Adenoviruses are ubiquitous human pathogens that cause a variety of diseases, such as respiratory infections, gastroenteritis, and conjunctivitis. While often viewed as a self-limiting infection in healthy individuals, adenoviruses are particularly harmful to immunocompromised patients. Here, we investigate the functional role of post-translational modifications (PTMs) on an essential adenovirus core protein, protein VII, describing how they regulate its function during the early and late stages of infection. Our study focuses on how specific PTMs on protein VII influence transcription, localization, and interactions with other proteins, highlighting how PTMs are employed by viruses to alter protein function.

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在腺病毒感染的早期阶段,蛋白VII的翻译后修饰是重要的。
由于翻译后修饰(PTM)在细胞功能中的重要性,病毒已经进化到既能利用这种修饰,又容易受到这种修饰的影响。腺病毒编码一种称为蛋白VII的多功能蛋白,该蛋白与病毒基因组一起包装在病毒粒子的核心,并在感染期间破坏宿主的染色质。蛋白VII有几个ptm,它们的加入有助于蛋白VII的亚核定位。在这里,我们使用突变病毒来消除或模拟蛋白VII上的这些ptm,以询问它们在腺病毒感染期间对蛋白VII功能的影响。我们发现位置2或3 (K2或K3)赖氨酸的乙酰化在早期感染期间是有害的,因为丙氨酸突变导致蛋白质VII和病毒DNA更多地摄入到细胞核,并增强了早期基因表达。此外,我们确定蛋白VII在感染后期的替代残基上乙酰化,这可能补偿突变位点。最后,由于早期病毒蛋白E1A在病毒基因激活中的作用,我们研究了蛋白VII和E1A之间的相互作用,并证明蛋白VII通过染色质介导的相互作用与E1A相互作用。总之,这些结果强调病毒-宿主相互作用的复杂性与翻译后修饰密切相关。重要性:腺病毒是普遍存在的人类病原体,可引起多种疾病,如呼吸道感染、肠胃炎和结膜炎。虽然腺病毒通常被视为健康人的自限性感染,但对免疫功能低下的患者尤其有害。在这里,我们研究了翻译后修饰(PTMs)对腺病毒核心蛋白蛋白VII的功能作用,描述了它们如何在感染的早期和晚期调节其功能。我们的研究重点是蛋白质VII上特异性PTMs如何影响转录、定位和与其他蛋白质的相互作用,强调PTMs如何被病毒利用来改变蛋白质功能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Virology
Journal of Virology 医学-病毒学
CiteScore
10.10
自引率
7.40%
发文量
906
审稿时长
1 months
期刊介绍: Journal of Virology (JVI) explores the nature of the viruses of animals, archaea, bacteria, fungi, plants, and protozoa. We welcome papers on virion structure and assembly, viral genome replication and regulation of gene expression, genetic diversity and evolution, virus-cell interactions, cellular responses to infection, transformation and oncogenesis, gene delivery, viral pathogenesis and immunity, and vaccines and antiviral agents.
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