Herpes simplex virus type 1 reshapes host chromatin architecture via transcription machinery hijacking
Herpes simplex virus type 1 (HSV-1) remodels the host chromatin structure and induces a host-to-virus transcriptional switch during lytic infection. We combine super-resolution imaging and chromosome-capture technologies to identify the mechanism of remodeling. We show that the host chromatin underg...
| Autores: | , , , , , , , |
|---|---|
| Tipo de recurso: | artículo |
| Estado: | Versión publicada |
| Fecha de publicación: | 2025 |
| País: | España |
| Institución: | Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya) |
| Repositorio: | Recercat. Dipósit de la Recerca de Catalunya |
| OAI Identifier: | oai:recercat.cat:10230/71155 |
| Acceso en línea: | http://hdl.handle.net/10230/71155 http://dx.doi.org/10.1038/s41467-025-60534-6 |
| Access Level: | acceso abierto |
| Palabra clave: | Chromatin Nuclear organization Single-molecule biophysics |
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Herpes simplex virus type 1 reshapes host chromatin architecture via transcription machinery hijacking |
| title |
Herpes simplex virus type 1 reshapes host chromatin architecture via transcription machinery hijacking |
| spellingShingle |
Herpes simplex virus type 1 reshapes host chromatin architecture via transcription machinery hijacking González-Almela, Esther Chromatin Nuclear organization Single-molecule biophysics |
| title_short |
Herpes simplex virus type 1 reshapes host chromatin architecture via transcription machinery hijacking |
| title_full |
Herpes simplex virus type 1 reshapes host chromatin architecture via transcription machinery hijacking |
| title_fullStr |
Herpes simplex virus type 1 reshapes host chromatin architecture via transcription machinery hijacking |
| title_full_unstemmed |
Herpes simplex virus type 1 reshapes host chromatin architecture via transcription machinery hijacking |
| title_sort |
Herpes simplex virus type 1 reshapes host chromatin architecture via transcription machinery hijacking |
| dc.creator.none.fl_str_mv |
González-Almela, Esther Castells García, Àlvaro, 1991- Le Dily, François Fernández Merino, Manuel Carnevali, Davide Cuscó Pons, Pol, 1987- Di Croce, Luciano Cosma, Maria Pia |
| author |
González-Almela, Esther |
| author_facet |
González-Almela, Esther Castells García, Àlvaro, 1991- Le Dily, François Fernández Merino, Manuel Carnevali, Davide Cuscó Pons, Pol, 1987- Di Croce, Luciano Cosma, Maria Pia |
| author_role |
author |
| author2 |
Castells García, Àlvaro, 1991- Le Dily, François Fernández Merino, Manuel Carnevali, Davide Cuscó Pons, Pol, 1987- Di Croce, Luciano Cosma, Maria Pia |
| author2_role |
author author author author author author author |
| dc.subject.none.fl_str_mv |
Chromatin Nuclear organization Single-molecule biophysics |
| topic |
Chromatin Nuclear organization Single-molecule biophysics |
| description |
Herpes simplex virus type 1 (HSV-1) remodels the host chromatin structure and induces a host-to-virus transcriptional switch during lytic infection. We combine super-resolution imaging and chromosome-capture technologies to identify the mechanism of remodeling. We show that the host chromatin undergoes massive condensation caused by the hijacking of RNA polymerase II (RNAP II) and topoisomerase I (TOP1). In addition, HSV-1 infection results in the rearrangement of topologically associating domains and loops, although the A/B compartments are maintained in the host. The position of viral genomes and their association with RNAP II and cohesin is determined nanometrically. We reveal specific host-HSV-1 genome interactions and enrichment of upregulated human genes in the most contacting regions. Finally, TOP1 inhibition fully blocks HSV-1 infection, suggesting possible antiviral strategies. This viral mechanism of host chromatin rewiring sheds light on the role of transcription in chromatin architecture. |
| publishDate |
2025 |
| dc.date.none.fl_str_mv |
2025 2025 2025 |
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info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion |
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article |
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publishedVersion |
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http://hdl.handle.net/10230/71155 http://dx.doi.org/10.1038/s41467-025-60534-6 http://hdl.handle.net/10230/71155 |
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http://hdl.handle.net/10230/71155 http://dx.doi.org/10.1038/s41467-025-60534-6 |
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Inglés |
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Inglés |
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Nat Commun. 2025 Jun 19;16(1):5313 info:eu-repo/grantAgreement/ES/2PE/PID2020-114080GB I00 info:eu-repo/grantAgreement/ES/2PE/PID2019-108322GB-100 info:eu-repo/grantAgreement/ES/2PE/BFU2017-86760-P |
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http://creativecommons.org/licenses/by-nc-nd/4.0/ info:eu-repo/semantics/openAccess |
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http://creativecommons.org/licenses/by-nc-nd/4.0/ |
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openAccess |
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application/pdf application/pdf |
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Nature Research |
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Nature Research |
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reponame:Recercat. Dipósit de la Recerca de Catalunya instname:Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya) |
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Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya) |
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Recercat. Dipósit de la Recerca de Catalunya |
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1869404260478746624 |
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Herpes simplex virus type 1 reshapes host chromatin architecture via transcription machinery hijackingGonzález-Almela, EstherCastells García, Àlvaro, 1991-Le Dily, FrançoisFernández Merino, ManuelCarnevali, DavideCuscó Pons, Pol, 1987-Di Croce, LucianoCosma, Maria PiaChromatinNuclear organizationSingle-molecule biophysicsHerpes simplex virus type 1 (HSV-1) remodels the host chromatin structure and induces a host-to-virus transcriptional switch during lytic infection. We combine super-resolution imaging and chromosome-capture technologies to identify the mechanism of remodeling. We show that the host chromatin undergoes massive condensation caused by the hijacking of RNA polymerase II (RNAP II) and topoisomerase I (TOP1). In addition, HSV-1 infection results in the rearrangement of topologically associating domains and loops, although the A/B compartments are maintained in the host. The position of viral genomes and their association with RNAP II and cohesin is determined nanometrically. We reveal specific host-HSV-1 genome interactions and enrichment of upregulated human genes in the most contacting regions. Finally, TOP1 inhibition fully blocks HSV-1 infection, suggesting possible antiviral strategies. This viral mechanism of host chromatin rewiring sheds light on the role of transcription in chromatin architecture.We acknowledge support from Innovative Team Program of Guangzhou Regenerative Medicine and Health Guangdong Laboratory (2018GZR110103001 to M.P.C.); Guangzhou Key Projects of Brain Science and Brain-Like Intelligence Technology (20200730009 to M.P.C.); National Natural Science Foundation of China (31971177 and 32270577 to M.P.C., 3221101299 to A.C.G.); Science and Technology Program of Guangzhou, China (202002030146 to M.P.C.); Guangdong Foreign Young Talent Program (WGZJXM04 to A.C.G.); Spanish Ministry of Science and Innovation (grant no. PID2020-114080GB I00/AEI/10.13039/501100011033 and grant no. BFU2017-86760-P/AEI/FEDER, UE to M.P.C.) and an AGAUR grant from the Department of Research and Universities of Generalitat de Catalunya (2021-SGR2021-01300 to M.P.C.); Spanish Ministry of Science and Innovation to the European Molecular Biology Laboratory (EMBL) partnership (to M.P.C.); the Spanish Ministry of Science and Innovation through the Centro de Excelencia Severo Ochoa (CEX2020-001049-S, MCIN?AEI /10.13039/501100011033); European Social Fund (FI_B00103 to M.F.M.). Funding for open access charge: National Natural Science Foundation of China (NSFC) grant (3221101299 to A.C.G.).; Spanish Ministry of Economy, Industry and Competitiveness (PID2019-108322GB-100 to L.D.C.).Nature Research202520252025info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfapplication/pdfhttp://hdl.handle.net/10230/71155http://dx.doi.org/10.1038/s41467-025-60534-6http://hdl.handle.net/10230/71155reponame:Recercat. Dipósit de la Recerca de Catalunyainstname:Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya)InglésNat Commun. 2025 Jun 19;16(1):5313info:eu-repo/grantAgreement/ES/2PE/PID2020-114080GB I00info:eu-repo/grantAgreement/ES/2PE/PID2019-108322GB-100info:eu-repo/grantAgreement/ES/2PE/BFU2017-86760-P© The Author(s) 2025. Open Access This article is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License, which permits any non-commercial use, sharing, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if you modified the licensed material. You do not have permission under this licence to share adapted material derived from this article or parts of it. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by-nc-nd/4.0/.http://creativecommons.org/licenses/by-nc-nd/4.0/info:eu-repo/semantics/openAccessoai:recercat.cat:10230/711552026-05-29T05:05:01Z |
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