Liquid–liquid phase separation of LARP7 restrains HIV-1 replication

HIV-1 initiates replication by its transactivator Tat, hijacking the positive transcription elongation factor b (P-TEFb) in the host cell. Most P-TEFb is maintained in an inactive state by 7SK snRNP until it is brought to the transcription initiation complex by cellular or viral transactivators that accelerate transcription and facilitate the production of full-length viral transcripts. Here, we report that HIV-1 infection triggers liquid-liquid phase separation of LARP7, a central component of 7SK snRNP. Tat is incorporated into HIV-1-induced LARP7 condensates after infection. Conserved lysine residues in the intrinsically disordered region of LARP7 are essential for both its phase separation and the inhibition of Tat-mediated transcription. These findings identify a mechanism wherein P-TEFb and Tat are sequestered within LARP7 condensates, restraining HIV-1 transcription.

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Publication Details

Journal
EMBO Reports
Published
2025-03-20
DOI
https://doi.org/10.1038/s44319-025-00421-9
Citations
2
Primary Topic
RNA Research and Splicing
Type
article
Field-Weighted Citation Impact
1.61

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article

Liquid–liquid phase separation of LARP7 restrains HIV-1 replication

Weihua Li, Zhuoxin Li, Bing Zhao, Xiya Fang et al.
2 citations
EMBO Reports
RNA Research and Splicing
1.61
article

Liquid–liquid phase separation of LARP7 restrains HIV-1 replication

Weihua Li, Zhuoxin Li, Bing Zhao, Xiya Fang, Ailing Li, Tao Zhou, Teng Li, Zeng-Lin Guo, Ran Liu, Wen Wang, Tingting Li, Yining Wang, Kai You Wang, Xin Xu, Qiuying Han, Yezhuang Shen, Biyu Zhang, Libing Yin, Weili Gong
article en
2 citations

Abstract

HIV-1 initiates replication by its transactivator Tat, hijacking the positive transcription elongation factor b (P-TEFb) in the host cell. Most P-TEFb is maintained in an inactive state by 7SK snRNP until it is brought to the transcription initiation complex by cellular or viral transactivators that accelerate transcription and facilitate the production of full-length viral transcripts. Here, we report that HIV-1 infection triggers liquid-liquid phase separation of LARP7, a central component of 7SK snRNP. Tat is incorporated into HIV-1-induced LARP7 condensates after infection. Conserved lysine residues in the intrinsically disordered region of LARP7 are essential for both its phase separation and the inhibition of Tat-mediated transcription. These findings identify a mechanism wherein P-TEFb and Tat are sequestered within LARP7 condensates, restraining HIV-1 transcription.

EMBO ReportsVol. 26(8)
Shanghai Medical College of Fudan University (CN), Fudan University (CN), National Center of Biomedical Analysis (CN), Zhejiang University (CN)
National Outstanding Youth Science Fund Project of National Natural Science Foundation of China
Good health and well-being
Openalex Percentile: Top 18%
RNA Research and Splicing
1.61
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