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HIV-1 整合酶的多模态功能。

Multimodal Functionalities of HIV-1 Integrase.

机构信息

Department of Cancer Immunology and Virology, Dana-Farber Cancer Institute, Boston, MA 02215, USA.

Department of Medicine, Harvard Medical School, Boston, MA 02115, USA.

出版信息

Viruses. 2022 Apr 28;14(5):926. doi: 10.3390/v14050926.

DOI:10.3390/v14050926
PMID:35632668
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9144474/
Abstract

Integrase is the retroviral protein responsible for integrating reverse transcripts into cellular genomes. Co-packaged with viral RNA and reverse transcriptase into capsid-encased viral cores, human immunodeficiency virus 1 (HIV-1) integrase has long been implicated in reverse transcription and virion maturation. However, the underlying mechanisms of integrase in these non-catalytic-related viral replication steps have remained elusive. Recent results have shown that integrase binds genomic RNA in virions, and that mutational or pharmacological disruption of integrase-RNA binding yields eccentric virion particles with ribonucleoprotein complexes situated outside of the capsid shell. Such viruses are defective for reverse transcription due to preferential loss of integrase and viral RNA from infected target cells. Parallel research has revealed defective integrase-RNA binding and eccentric particle formation as common features of class II integrase mutant viruses, a phenotypic grouping of viruses that display defects at steps beyond integration. In light of these new findings, we propose three new subclasses of class II mutant viruses (a, b, and c), all of which are defective for integrase-RNA binding and particle morphogenesis, but differ based on distinct underlying mechanisms exhibited by the associated integrase mutant proteins. We also assess how these findings inform the role of integrase in HIV-1 particle maturation.

摘要

整合酶是负责将逆转录病毒的 RNA 逆转录整合到宿主细胞基因组中的病毒蛋白。人类免疫缺陷病毒 1(HIV-1)整合酶与病毒 RNA 和逆转录酶一起被包装到衣壳包裹的病毒核心中,长期以来一直与逆转录和病毒成熟有关。然而,整合酶在这些非催化相关的病毒复制步骤中的潜在机制仍然难以捉摸。最近的研究结果表明,整合酶与病毒粒子中的基因组 RNA 结合,并且整合酶-RNA 结合的突变或药理学破坏会产生偏心的病毒粒子,其核糖核蛋白复合物位于衣壳壳之外。由于感染靶细胞中整合酶和病毒 RNA 的优先丢失,此类病毒在逆转录过程中存在缺陷。平行研究还揭示了缺陷的整合酶-RNA 结合和偏心颗粒形成是 II 类整合酶突变病毒的共同特征,这是一组在整合步骤之外表现出缺陷的病毒的表型分组。鉴于这些新发现,我们提出了三种新的 II 类突变病毒亚类(a、b 和 c),它们都不能与 RNA 结合并形成颗粒形态,但由于相关整合酶突变蛋白表现出不同的潜在机制而有所不同。我们还评估了这些发现如何影响整合酶在 HIV-1 颗粒成熟中的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34c3/9144474/3e9698a084c0/viruses-14-00926-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34c3/9144474/868fa57fa808/viruses-14-00926-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34c3/9144474/e3207dd19360/viruses-14-00926-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34c3/9144474/dfcd2825f35f/viruses-14-00926-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34c3/9144474/f227f5db6969/viruses-14-00926-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34c3/9144474/c5e7a66be4a3/viruses-14-00926-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34c3/9144474/3e9698a084c0/viruses-14-00926-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34c3/9144474/868fa57fa808/viruses-14-00926-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34c3/9144474/e3207dd19360/viruses-14-00926-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34c3/9144474/dfcd2825f35f/viruses-14-00926-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34c3/9144474/f227f5db6969/viruses-14-00926-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34c3/9144474/c5e7a66be4a3/viruses-14-00926-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34c3/9144474/3e9698a084c0/viruses-14-00926-g005.jpg

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