Department of Infectious Diseases, Virology, Heidelberg University, Heidelberg, Germany; email:
German Center for Infection Research, Heidelberg, Germany.
Annu Rev Virol. 2022 Sep 29;9(1):261-284. doi: 10.1146/annurev-virology-020922-110929. Epub 2022 Jun 15.
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.
病毒进入细胞后,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、亚病毒复合物在没有核膜破裂的情况下进入细胞核,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,表明逆转录的完成和病毒基因组脱壳发生在细胞核中,而不是以前认为的细胞质中,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,锥形衣壳不仅作为逆转录的反应容器和抵御先天免疫传感器的保护罩,而且可能构成难以捉摸的 HIV-1 核输入因子。衣壳的破裂可能是由逆转录的完成、未知的核因子或物理损伤触发的,而且似乎与整合过程密切相关。