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PARP1 associates with R-loops to promote their resolution and genome stability
PARP1 is a DNA-dependent ADP-Ribose transferase with ADP-ribosylation activity that is triggered by DNA breaks and non-B DNA structures to mediate their resolution. PARP1 was also recently identified as a component of the R-loop-associated protein-protein interaction network, suggesting a potential...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10018367/ https://www.ncbi.nlm.nih.gov/pubmed/36794853 http://dx.doi.org/10.1093/nar/gkad066 |
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author | Laspata, Natalie Kaur, Parminder Mersaoui, Sofiane Yacine Muoio, Daniela Liu, Zhiyan Silvia Bannister, Maxwell Henry Nguyen, Hai Dang Curry, Caroline Pascal, John M Poirier, Guy G Wang, Hong Masson, Jean-Yves Fouquerel, Elise |
author_facet | Laspata, Natalie Kaur, Parminder Mersaoui, Sofiane Yacine Muoio, Daniela Liu, Zhiyan Silvia Bannister, Maxwell Henry Nguyen, Hai Dang Curry, Caroline Pascal, John M Poirier, Guy G Wang, Hong Masson, Jean-Yves Fouquerel, Elise |
author_sort | Laspata, Natalie |
collection | PubMed |
description | PARP1 is a DNA-dependent ADP-Ribose transferase with ADP-ribosylation activity that is triggered by DNA breaks and non-B DNA structures to mediate their resolution. PARP1 was also recently identified as a component of the R-loop-associated protein-protein interaction network, suggesting a potential role for PARP1 in resolving this structure. R-loops are three-stranded nucleic acid structures that consist of a RNA–DNA hybrid and a displaced non-template DNA strand. R-loops are involved in crucial physiological processes but can also be a source of genome instability if persistently unresolved. In this study, we demonstrate that PARP1 binds R-loops in vitro and associates with R-loop formation sites in cells which activates its ADP-ribosylation activity. Conversely, PARP1 inhibition or genetic depletion causes an accumulation of unresolved R-loops which promotes genomic instability. Our study reveals that PARP1 is a novel sensor for R-loops and highlights that PARP1 is a suppressor of R-loop-associated genomic instability. |
format | Online Article Text |
id | pubmed-10018367 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-100183672023-03-17 PARP1 associates with R-loops to promote their resolution and genome stability Laspata, Natalie Kaur, Parminder Mersaoui, Sofiane Yacine Muoio, Daniela Liu, Zhiyan Silvia Bannister, Maxwell Henry Nguyen, Hai Dang Curry, Caroline Pascal, John M Poirier, Guy G Wang, Hong Masson, Jean-Yves Fouquerel, Elise Nucleic Acids Res Genome Integrity, Repair and Replication PARP1 is a DNA-dependent ADP-Ribose transferase with ADP-ribosylation activity that is triggered by DNA breaks and non-B DNA structures to mediate their resolution. PARP1 was also recently identified as a component of the R-loop-associated protein-protein interaction network, suggesting a potential role for PARP1 in resolving this structure. R-loops are three-stranded nucleic acid structures that consist of a RNA–DNA hybrid and a displaced non-template DNA strand. R-loops are involved in crucial physiological processes but can also be a source of genome instability if persistently unresolved. In this study, we demonstrate that PARP1 binds R-loops in vitro and associates with R-loop formation sites in cells which activates its ADP-ribosylation activity. Conversely, PARP1 inhibition or genetic depletion causes an accumulation of unresolved R-loops which promotes genomic instability. Our study reveals that PARP1 is a novel sensor for R-loops and highlights that PARP1 is a suppressor of R-loop-associated genomic instability. Oxford University Press 2023-02-16 /pmc/articles/PMC10018367/ /pubmed/36794853 http://dx.doi.org/10.1093/nar/gkad066 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of Nucleic Acids Research. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Genome Integrity, Repair and Replication Laspata, Natalie Kaur, Parminder Mersaoui, Sofiane Yacine Muoio, Daniela Liu, Zhiyan Silvia Bannister, Maxwell Henry Nguyen, Hai Dang Curry, Caroline Pascal, John M Poirier, Guy G Wang, Hong Masson, Jean-Yves Fouquerel, Elise PARP1 associates with R-loops to promote their resolution and genome stability |
title | PARP1 associates with R-loops to promote their resolution and genome stability |
title_full | PARP1 associates with R-loops to promote their resolution and genome stability |
title_fullStr | PARP1 associates with R-loops to promote their resolution and genome stability |
title_full_unstemmed | PARP1 associates with R-loops to promote their resolution and genome stability |
title_short | PARP1 associates with R-loops to promote their resolution and genome stability |
title_sort | parp1 associates with r-loops to promote their resolution and genome stability |
topic | Genome Integrity, Repair and Replication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10018367/ https://www.ncbi.nlm.nih.gov/pubmed/36794853 http://dx.doi.org/10.1093/nar/gkad066 |
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