Nuclear Capsid Uncoating and Reverse Transcription of HIV-1.

IF 8.1 1区 医学 Q1 VIROLOGY Annual Review of Virology Pub Date : 2022-06-15 DOI:10.1146/annurev-virology-020922-110929
Thorsten G. Müller, V. Zila, B. Müller, H. Kräusslich
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引用次数: 13

Abstract

After cell entry, human immunodeficiency virus type 1 (HIV-1) replication involves reverse transcription of the RNA genome, nuclear import of the subviral complex without nuclear envelope breakdown, and integration of the viral complementary DNA into the host genome. Here, we discuss recent evidence indicating that completion of reverse transcription and viral genome uncoating occur in the nucleus rather than in the cytoplasm, as previously thought, and suggest a testable model for nuclear import and uncoating. Multiple recent studies indicated that the cone-shaped capsid, which encases the genome and replication proteins, not only serves as a reaction container for reverse transcription and as a shield from innate immune sensors but also may constitute the elusive HIV-1 nuclear import factor. Rupture of the capsid may be triggered in the nucleus by completion of reverse transcription, by yet-unknown nuclear factors, or by physical damage, and it appears to occur in close temporal and spatial association with the integration process. Expected final online publication date for the Annual Review of Virology, Volume 9 is September 2022. Please see http://www.annualreviews.org/page/journal/pubdates for revised estimates.
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HIV-1的核衣壳剥离和逆转录。
在进入细胞后,人类免疫缺陷病毒1型(HIV-1)的复制包括RNA基因组的逆转录,亚病毒复合体的核输入而不破坏核膜,以及病毒互补DNA整合到宿主基因组中。在这里,我们讨论了最近的证据表明,逆转录完成和病毒基因组脱壳发生在细胞核而不是细胞质中,如以前认为的那样,并提出了一个可测试的核输入和脱壳模型。最近的多项研究表明,包裹着基因组和复制蛋白的锥形衣壳不仅是逆转录的反应容器和对先天免疫传感器的屏蔽,而且可能是难以捉摸的HIV-1核输入因子。在细胞核中,逆转录的完成、未知的核因子或物理损伤可能触发衣壳破裂,并且与整合过程在时间和空间上密切相关。《病毒学年度评论》第9卷的最终在线出版日期预计为2022年9月。修订后的估计数请参阅http://www.annualreviews.org/page/journal/pubdates。
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
CiteScore
19.40
自引率
0.90%
发文量
28
期刊介绍: The Annual Review of Virology serves as a conduit for disseminating thrilling advancements in our comprehension of viruses spanning animals, plants, bacteria, archaea, fungi, and protozoa. Its reviews illuminate novel concepts and trajectories in basic virology, elucidating viral disease mechanisms, exploring virus-host interactions, and scrutinizing cellular and immune responses to virus infection. These reviews underscore the exceptional capacity of viruses as potent probes for investigating cellular function.
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