Long Noncoding RNA LINC02453 Inhibits HIV‐1 Replication by Binding With SEC13 to Regulate the Viral Productive Cycle

Emerging evidence underscores the pivotal role of long noncoding RNAs (lncRNAs) as crucial regulators within the HIV life cycle. However, the precise functions and detailed mechanisms by which lncRNAs operate in HIV-1 highly exposed but persistently seronegative (HESN) individuals remain currently unknown. Through RNA sequencing analysis of the HESN individual and the matched control, we identified potential lncRNAs. Then, we conducted validation experiments at the population level, while cellular models of HIV-1 infection were constructed for functional experimental investigations in vitro. Subcellular localization of the identified lncRNA was determined, followed by an exploration of the specific regulatory mechanism underlying HIV resistance through some experiments, such as RNA pull-down, western blot and Hirt assays. LncRNA LINC02453 is highly expressed in HESN. Moreover, LINC02453 is identified as a novel lncRNA associated with heightened resistance to HIV-1. LINC02453 is predominantly localized in the nucleus and binds to SEC13, a component of the nuclear pore complex, leading to the inhibition of HIV-1 replication by regulating key processes such as late reverse transcription, nuclear import, and DNA integration. Our findings suggest that LINC02453 may serve as a prospective target for the development of innovative anti-HIV therapeutics.

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Publication Details

Journal
Journal of Medical Virology
Published
2024-12-01
DOI
https://doi.org/10.1002/jmv.70116
Citations
1
Primary Topic
Cancer-related molecular mechanisms research
Type
article
Field-Weighted Citation Impact
0.29
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article

Long Noncoding RNA LINC02453 Inhibits HIV‐1 Replication by Binding With SEC13 to Regulate the Viral Productive Cycle

Chen Xiu, Tongxue Qin, Liufang Wen, Junjun Jiang et al.
1 citations
Journal of Medical Virology
Cancer-related molecular mechanisms research
0.29
article

Long Noncoding RNA LINC02453 Inhibits HIV‐1 Replication by Binding With SEC13 to Regulate the Viral Productive Cycle

Chen Xiu, Tongxue Qin, Liufang Wen, Junjun Jiang, Wudi Wei, Rongfeng Chen, Jinmiao Li, Hao Liang, Yinlu Liao, Xing Tao, Jinming Su, Ye Li, Youjin Huang, Wenfei Wei, Zongxiang Yuan, Jie Liu
article en
1 citations

Abstract

Emerging evidence underscores the pivotal role of long noncoding RNAs (lncRNAs) as crucial regulators within the HIV life cycle. However, the precise functions and detailed mechanisms by which lncRNAs operate in HIV-1 highly exposed but persistently seronegative (HESN) individuals remain currently unknown. Through RNA sequencing analysis of the HESN individual and the matched control, we identified potential lncRNAs. Then, we conducted validation experiments at the population level, while cellular models of HIV-1 infection were constructed for functional experimental investigations in vitro. Subcellular localization of the identified lncRNA was determined, followed by an exploration of the specific regulatory mechanism underlying HIV resistance through some experiments, such as RNA pull-down, western blot and Hirt assays. LncRNA LINC02453 is highly expressed in HESN. Moreover, LINC02453 is identified as a novel lncRNA associated with heightened resistance to HIV-1. LINC02453 is predominantly localized in the nucleus and binds to SEC13, a component of the nuclear pore complex, leading to the inhibition of HIV-1 replication by regulating key processes such as late reverse transcription, nuclear import, and DNA integration. Our findings suggest that LINC02453 may serve as a prospective target for the development of innovative anti-HIV therapeutics.

Journal of Medical VirologyVol. 96(12)
Guangxi Medical University (CN)
Responsible consumption and production
Openalex Percentile: Top 37%
Cancer-related molecular mechanisms research
0.29
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