HIV-1转录起始位点的使用及其对HIV感染者非剪接RNA功能的影响

IF 5.1 1区 生物学 Q1 MICROBIOLOGY
mBio Pub Date : 2025-02-05 Epub Date: 2024-12-27 DOI:10.1128/mbio.03576-24
Saiful Islam, Frank Maldarelli, Olga A Nikolaitchik, Zetao Cheng, Robert Gorelick, Maria A Nikolaitchik, Vinay K Pathak, Wei-Shau Hu
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引用次数: 0

摘要

HIV-1非剪接RNA在病毒复制过程中有两种不同的功能:它被包装成颗粒作为病毒基因组,它被翻译成病毒组装所需的Gag/Gag- pol多蛋白。最近的研究表明,在培养的细胞中,HIV-1使用多个转录起始位点产生几种未剪接的RNA,包括两个主要的转录物,分别具有3个和1个5'鸟苷,分别称为3G和1G RNA。虽然几乎相同,但1G RNA比3G RNA被选择包装为病毒粒子基因组,这表明这些RNA物种在功能上是不同的。目前,我们对HIV-1转录起始位点的使用和RNA物种功能的理解是基于培养细胞的研究。在这里,我们检查了HIV感染者的样本,以研究HIV-1转录起始位点的使用及其对RNA功能的影响。使用在同一日期从同一参与者收集的成对样本,我们检查了感染细胞(PBMC)和病毒(血浆)中的HIV-1未剪接RNA种类。我们的研究结果表明,在艾滋病毒感染者中,病毒使用多个转录起始位点产生几种非剪接转录物,包括3G和1G RNA。此外,我们在配对的血浆样品中观察到1G RNA的富集,表明1G RNA在体内的优先包装。我们的研究阐明了HIV-1非剪接RNA在HIV感染者体内的复杂调控,并为HIV-1非剪接RNA在体内如何发挥作用提供了有价值的见解。hiv -1病毒粒子必须含有未剪接的RNA及其翻译产物以维持感染性。HIV-1非剪接RNA如何在病毒复制中发挥这两个重要而又不同的作用一直是该领域一个长期存在的问题。在本报告中,我们证明了在HIV感染者中,病毒使用多个转录起始位点来产生几种未剪接的RNA,这些RNA在序列上99%相同,但在功能上不同。其中一种RNA, 1G RNA,比其他HIV-1非剪接RNA被选择包装成病毒颗粒。这些发现与先前基于细胞培养的观察结果一致,并为HIV-1如何调节其未剪接RNA在HIV感染者中的功能提供了见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
HIV-1 transcription start sites usage and its impact on unspliced RNA functions in people living with HIV.

HIV-1 unspliced RNA serves two distinct functions during viral replication: it is packaged into particles as the viral genome, and it is translated to generate Gag/Gag-Pol polyproteins required for virus assembly. Recent studies have demonstrated that in cultured cells, HIV-1 uses multiple transcription start sites to generate several unspliced RNA species, including two major transcripts with three and one 5' guanosine, referred to as 3G and 1G RNA, respectively. Although nearly identical, 1G RNA is selected over 3G RNA to be packaged as the virion genome, indicating that these RNA species are functionally distinct. Currently, our understanding of HIV-1 transcription start site usage and the functions of RNA species is based on studies using cultured cells. Here, we examined samples from people living with HIV to investigate HIV-1 transcription start site usage and its impact on RNA function. Using paired samples collected from the same participants on the same date, we examined the HIV-1 unspliced RNA species in infected cells (PBMC) and in viruses (plasma). Our findings demonstrate that in people living with HIV, the virus uses multiple transcription start sites to generate several unspliced transcripts, including 3G and 1G RNA. Furthermore, we observed an enrichment of 1G RNA in the paired plasma samples, indicating a preferential packaging of 1G RNA in vivo. Our study illustrates the complex regulation of HIV-1 unspliced RNA in people living with HIV and provides valuable insights into how HIV-1 unspliced RNAs serve their functions in vivo.IMPORTANCEHIV-1 virions must contain unspliced RNA and its translation products to maintain infectivity. How HIV-1 unspliced RNA fulfills these two essential and yet distinct roles in viral replication has been a long-standing question in the field. In this report, we demonstrate that in people living with HIV, the virus uses multiple transcription start sites to generate several unspliced RNA species that are 99% identical in sequence but differ functionally. One of the RNA species, 1G RNA, is selected over other HIV-1 unspliced RNAs to be packaged into viral particles. These findings are consistent with previous cell-culture-based observations and provide insights into how HIV-1 regulates its unspliced RNA function in people living with HIV.

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来源期刊
mBio
mBio MICROBIOLOGY-
CiteScore
10.50
自引率
3.10%
发文量
762
审稿时长
1 months
期刊介绍: mBio® is ASM''s first broad-scope, online-only, open access journal. mBio offers streamlined review and publication of the best research in microbiology and allied fields.
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