Please use this identifier to cite or link to this item: http://bura.brunel.ac.uk/handle/2438/32385
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dc.contributor.authorPenzo, C-
dc.contributor.authorÖzel, I-
dc.contributor.authorMartinovic, M-
dc.contributor.authorKuzman, M-
dc.contributor.authorGlavas, D-
dc.contributor.authorStanic, M-
dc.contributor.authorReichenbach, T-
dc.contributor.authorMüller, TG-
dc.contributor.authorRheinberger, M-
dc.contributor.authorGodarzi, N-
dc.contributor.authorLapaillerie, D-
dc.contributor.authorSrezovic, B-
dc.contributor.authordell’Oca, MC-
dc.contributor.authorLange, LC-
dc.contributor.authorSadhu, L-
dc.contributor.authorde Castro, IJ-
dc.contributor.authorShytaj, IL-
dc.contributor.authorForcato, M-
dc.contributor.authorLaketa, V-
dc.contributor.authorBicciato, S-
dc.contributor.authorVlahovicek, K-
dc.contributor.authorFackler, OT-
dc.contributor.authorLucic, B-
dc.contributor.authorPena, V-
dc.contributor.authorKräusslich, H-G-
dc.contributor.authorParissi, V-
dc.contributor.authorLusic, M-
dc.date.accessioned2025-11-21T15:36:09Z-
dc.date.available2025-11-21T15:36:09Z-
dc.date.issued2025-08-20-
dc.identifierORCiD: Maja Kuzman https://orcid.org/0000-0002-7490-450X-
dc.identifierORCiD: Mia Stanic https://orcid.org/0000-0003-2149-2916-
dc.identifierORCiD: Thorsten G. Müller https://orcid.org/0000-0002-4197-6224-
dc.identifierORCiD: Maria Chiara dell’Oca https://orcid.org/0009-0003-3722-7057-
dc.identifierORCiD: Inês de Castro https://orcid.org/0000-0001-8710-3667-
dc.identifierORCiD: Iart Luca Shytaj https://orcid.org/0000-0002-9980-1275-
dc.identifierORCiD: Silvio Bicciato https://orcid.org/0000-0002-1944-7078-
dc.identifierORCiD: Oliver T. Fackler https://orcid.org/0000-0003-2982-4209-
dc.identifierORCiD: Vincent Parissi https://orcid.org/0000-0003-1661-7841-
dc.identifierORCiD: Marina Lusic https://orcid.org/0000-0002-0120-3569-
dc.identifier.citationPenzo, 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.en_US
dc.identifier.urihttps://bura.brunel.ac.uk/handle/2438/32385-
dc.descriptionData 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.en_US
dc.descriptionCode 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.-
dc.descriptionExtended data are available online at: https://www.nature.com/articles/s41564-025-02089-2#Sec44 .-
dc.descriptionSupplementary information is available online at: https://www.nature.com/articles/s41564-025-02089-2#Sec45 .-
dc.descriptionSource data are available online at: https://www.nature.com/articles/s41564-025-02089-2#Sec46 .-
dc.description.abstractHIV-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.en_US
dc.description.sponsorshipThis research was supported by DFG SFB1129 Deutsche Forschungsgemeinschaft (DFG, German Research Foundation) Project number 240245660-SFB 1129, Project 20 to M.L., by the DFG Priority Program (SPP2202 3D Genome Architecture in Development and Diseases Project ‘Nuclear landscape of HIV-1 infection in microglia—an unexplored HIV reservoir’ 422856668) to M.L., by DFG Project number 455044444 ‘Unraveling epigenetic and metabolic interplay during cell fate transition of HIV-1 infected T cells’ to M.L. and B.L., and by the German Center for Infection Research, DZIF (TTU04.820 (HIV reservoir) and TTU04.709 (Preclinical HIV-1 Research)), to M.L. and by R61DA059924 (NIH/NIDA) (M.L. co-PI). We acknowledge the Wellcome Trust for supporting V. Pena with grant 220300Z/20/Z. Funding for publication costs was provided by DFG SFB1129 Project number 240245660- SFB 1129, Project 20 to M.L.en_US
dc.format.extent2306 - 2322-
dc.format.mediumElectronic-
dc.languageEnglish-
dc.language.isoen_USen_US
dc.publisherSpringer Natureen_US
dc.rightsCopyright . Rights and permissions: Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. This is the accepted author manuscript (AAM) of the article which has been made Open Access under the University of Bristol's Scholarly Works Policy. The final published version (Version of Record) can be found on the publisher's website. The copyright of any third-party content, such as images, remains with the copyright holder.-
dc.subjectnuclear organizationen_US
dc.subjectretrovirusen_US
dc.subjectRNA:DNA hybrids-
dc.subjectR-loops-
dc.subjectHIV-1 integration-
dc.subjectHIV-1 integrase-
dc.subjectRNA helicase-
dc.subjectAquarius-
dc.subjectIntron Binding Complex (IBC)-
dc.titleAquarius helicase facilitates HIV-1 integration into R-loop enriched genomic regionsen_US
dc.typeArticleen_US
dc.date.dateAccepted2025-07-15-
dc.identifier.doihttps://doi.org/10.1038/s41564-025-02089-2-
dc.relation.isPartOfNature Microbiology-
pubs.publication-statusPublished-
pubs.volume10-
dc.identifier.eissn2058-5276-
dcterms.dateAccepted2025-07-15-
Appears in Collections:Brunel Medical School Research Papers

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