Department of Pathology and Laboratory Medicine, University of Wisconsin, Madison, Wisconsin, USA.
McArdle Laboratory for Cancer Research and Carbone Cancer Center, University of Wisconsin, Madison, Wisconsin, USA.
mBio. 2023 Dec 19;14(6):e0007023. doi: 10.1128/mbio.00070-23. Epub 2023 Nov 1.
Recent advances in the study of virus-cell interactions have improved our understanding of how viruses that replicate their genomes in the nucleus (e.g., retroviruses, hepadnaviruses, herpesviruses, and a subset of RNA viruses) hijack cellular pathways to export these genomes to the cytoplasm where they access virion egress pathways. These findings shed light on novel aspects of viral life cycles relevant to the development of new antiviral strategies and can yield new tractable, virus-based tools for exposing additional secrets of the cell. The goal of this review is to summarize defined and emerging modes of virus-host interactions that drive the transit of viral genomes out of the nucleus across the nuclear envelope barrier, with an emphasis on retroviruses that are most extensively studied. In this context, we prioritize discussion of recent progress in understanding the trafficking and function of the human immunodeficiency virus type 1 Rev protein, exemplifying a relatively refined example of stepwise, cooperativity-driven viral subversion of multi-subunit host transport receptor complexes.
近年来,病毒-细胞相互作用的研究进展提高了我们对以下方面的理解:病毒如何利用细胞途径将其在细胞核中复制基因组(例如逆转录病毒、嗜肝 DNA 病毒、疱疹病毒和一部分 RNA 病毒)输出到细胞质,从而进入病毒出芽途径。这些发现揭示了与开发新抗病毒策略相关的病毒生命周期的新方面,并为揭示细胞的更多秘密提供了新的、可行的基于病毒的工具。本文的目的是总结定义和新兴的病毒-宿主相互作用模式,这些模式驱动病毒基因组从细胞核穿过核膜屏障的运输,重点是研究最广泛的逆转录病毒。在这方面,我们优先讨论了近年来对人类免疫缺陷病毒 1 型 Rev 蛋白的运输和功能的理解进展,该蛋白是逐步、协同驱动病毒对多亚基宿主运输受体复合物进行颠覆的一个相对精细的例子。