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HIV-1 核心的核输入先于逆转录和脱壳。

Nuclear Import of the HIV-1 Core Precedes Reverse Transcription and Uncoating.

机构信息

Department of Microbiology and Immunology, Einstein, Bronx, NY 10461, USA.

Center for Cancer Research, National Cancer Institute at Frederick, Frederick, MD 21702-1201, USA.

出版信息

Cell Rep. 2020 Sep 29;32(13):108201. doi: 10.1016/j.celrep.2020.108201.

Abstract

HIV-1 reverse transcription (RT) occurs before or during uncoating, but the cellular compartment where RT and uncoating occurs is unknown. Using imaging and biochemical assays to track HIV-1 capsids in the nucleus during infection, we demonstrated that higher-order capsid complexes and/or complete cores containing the viral genome are imported into the nucleus. Inhibition of RT does not prevent capsid nuclear import; thus, RT may occur in nuclear compartments. Cytosolic and nuclear fractions of infected cells reveal that most RT intermediates are enriched in nuclear fractions, suggesting that HIV-1 RT occurs in the nucleus alongside uncoating. In agreement, we find that capsid in the nucleus induces recruitment of cleavage and polyadenylation specific factor 6 (CPSF6) to SC35 nuclear speckles, which are highly active transcription sites, suggesting that CPSF6 through capsid is recruiting viral complexes to SC35 speckles for the occurrence of RT. Thus, nuclear import precedes RT and uncoating, which fundamentally changes our understanding of HIV-1 infection.

摘要

HIV-1 逆转录 (RT) 发生在脱壳之前或期间,但 RT 和脱壳发生的细胞区室尚不清楚。通过在感染过程中使用成像和生化测定来追踪 HIV-1 衣壳在核内的情况,我们证明了更高阶的衣壳复合物和/或含有病毒基因组的完整核心被导入核内。RT 抑制剂不能阻止衣壳的核内输入;因此,RT 可能发生在核区室中。感染细胞的胞质和核部分揭示,大多数 RT 中间体在核部分中富集,这表明 HIV-1 RT 与脱壳同时发生在核内。一致地,我们发现核内的衣壳诱导切割和多聚腺苷酸化特异性因子 6 (CPSF6)募集到 SC35 核斑点,这是高度活跃的转录部位,这表明 CPSF6 通过衣壳将病毒复合物募集到 SC35 斑点以进行 RT。因此,核内输入先于 RT 和脱壳,这从根本上改变了我们对 HIV-1 感染的理解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/545b/7871456/6c4211ede699/nihms-1633682-f0001.jpg

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