Please use this identifier to cite or link to this item: http://bura.brunel.ac.uk/handle/2438/32385
Title: Aquarius helicase facilitates HIV-1 integration into R-loop enriched genomic regions
Authors: Penzo, C
Özel, I
Martinovic, M
Kuzman, M
Glavas, D
Stanic, M
Reichenbach, T
Müller, TG
Rheinberger, M
Godarzi, N
Lapaillerie, D
Srezovic, B
dell’Oca, MC
Lange, LC
Sadhu, L
de Castro, IJ
Shytaj, IL
Forcato, M
Laketa, V
Bicciato, S
Vlahovicek, K
Fackler, OT
Lucic, B
Pena, V
Kräusslich, H-G
Parissi, V
Lusic, M
Keywords: nuclear organization;retrovirus;RNA:DNA hybrids;R-loops;HIV-1 integration;HIV-1 integrase;RNA helicase;Aquarius;Intron Binding Complex (IBC)
Issue Date: 20-Aug-2025
Publisher: Springer Nature
Citation: Penzo, C. et al. (2025) 'Aquarius helicase facilitates HIV-1 integration into R-loop enriched genomic regions', Nature Microbiology, 10, pp. 2306 - 2322. doi: 10.1038/s41564-025-02089-2.
Abstract: HIV-1 integration into host chromosomes, essential for viral replication, is catalysed by viral integrase (IN). IN recurrently targets intronic regions of transcriptionally active genes, but a detailed understanding of this process is still unclear. Here, using ex vivo activated human primary CD4+T cells, we find that genomic RNA:DNA hybrids (R-loops) preferentially map to intronic regions of active genes that are typical HIV-1 integration sites. IN binds R-loops and their resolution enhances viral integration in vitro. We identify Aquarius (AQR), the splicing RNA helicase of the pentameric intron binding complex (IBC), which associates with IN and show that its RNA:DNA helicase activity promotes integration into hybrid substrates in vitro. Knockout of AQR in primary CD4+ T cells impaired overall integration efficiency, while sequencing of remaining integrations mapped them to intergenic and R-loop distal regions. These findings may have important implications for HIV-1 latency and reactivation and may thus identify novel therapeutic targets.
Description: Data availability: All relevant data supporting the key findings of this study are available within the article and its Supplementary Information files. BioProject and associated SRA metadata for DRIPc-seq from activated CD4+ T cells, as well as HIV-1 integration sites from AQR KO CD4 T cells and integration sites from siCTRL or siAQR HEK293T cells upon HIV-1 infection or MLV-based vector transduction, are available as part of the project PRJNA1055299 at https://dataview.ncbi.nlm.nih.gov/object/PRJNA1055299. The integration site sequencing data are also listed in Supplementary Tables 2 and 3. Source data are provided with this paper.
Code availability:All code accompanying this paper is available in GitHub at https://github.com/MaKuzman/R-loops-code (ref. 81) and https://github.com/bsrezovic/HIV_Rloops/ (ref. 82). There are no restrictions to code access.
Extended data are available online at: https://www.nature.com/articles/s41564-025-02089-2#Sec44 .
Supplementary information is available online at: https://www.nature.com/articles/s41564-025-02089-2#Sec45 .
Source data are available online at: https://www.nature.com/articles/s41564-025-02089-2#Sec46 .
URI: https://bura.brunel.ac.uk/handle/2438/32385
DOI: https://doi.org/10.1038/s41564-025-02089-2
Other Identifiers: ORCiD: Maja Kuzman https://orcid.org/0000-0002-7490-450X
ORCiD: Mia Stanic https://orcid.org/0000-0003-2149-2916
ORCiD: Thorsten G. Müller https://orcid.org/0000-0002-4197-6224
ORCiD: Maria Chiara dell’Oca https://orcid.org/0009-0003-3722-7057
ORCiD: Inês de Castro https://orcid.org/0000-0001-8710-3667
ORCiD: Iart Luca Shytaj https://orcid.org/0000-0002-9980-1275
ORCiD: Silvio Bicciato https://orcid.org/0000-0002-1944-7078
ORCiD: Oliver T. Fackler https://orcid.org/0000-0003-2982-4209
ORCiD: Vincent Parissi https://orcid.org/0000-0003-1661-7841
ORCiD: Marina Lusic https://orcid.org/0000-0002-0120-3569
Appears in Collections:Brunel Medical School Research Papers

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