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SUMO-mediated recruitment allows timely function of the Yen1 nuclease in mitotic cells

The post-translational modification of DNA damage response proteins with SUMO is an important mechanism to orchestrate a timely and orderly recruitment of repair factors to damage sites. After DNA replication stress and double-strand break formation, a number of repair factors are SUMOylated and int...

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Detalles Bibliográficos
Autores principales: Dorison, Hugo, Talhaoui, Ibtissam, Mazón, Gerard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8986097/
https://www.ncbi.nlm.nih.gov/pubmed/35333860
http://dx.doi.org/10.1371/journal.pgen.1009860
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author Dorison, Hugo
Talhaoui, Ibtissam
Mazón, Gerard
author_facet Dorison, Hugo
Talhaoui, Ibtissam
Mazón, Gerard
author_sort Dorison, Hugo
collection PubMed
description The post-translational modification of DNA damage response proteins with SUMO is an important mechanism to orchestrate a timely and orderly recruitment of repair factors to damage sites. After DNA replication stress and double-strand break formation, a number of repair factors are SUMOylated and interact with other SUMOylated factors, including the Yen1 nuclease. Yen1 plays a critical role in ensuring genome stability and unperturbed chromosome segregation by removing covalently linked DNA intermediates between sister chromatids that are formed by homologous recombination. Here we show how this important role of Yen1 depends on interactions mediated by non-covalent binding to SUMOylated partners. Mutations in the motifs that allow SUMO-mediated recruitment of Yen1 impair its ability to resolve DNA intermediates and result in chromosome mis-segregation and increased genome instability.
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spelling pubmed-89860972022-04-07 SUMO-mediated recruitment allows timely function of the Yen1 nuclease in mitotic cells Dorison, Hugo Talhaoui, Ibtissam Mazón, Gerard PLoS Genet Research Article The post-translational modification of DNA damage response proteins with SUMO is an important mechanism to orchestrate a timely and orderly recruitment of repair factors to damage sites. After DNA replication stress and double-strand break formation, a number of repair factors are SUMOylated and interact with other SUMOylated factors, including the Yen1 nuclease. Yen1 plays a critical role in ensuring genome stability and unperturbed chromosome segregation by removing covalently linked DNA intermediates between sister chromatids that are formed by homologous recombination. Here we show how this important role of Yen1 depends on interactions mediated by non-covalent binding to SUMOylated partners. Mutations in the motifs that allow SUMO-mediated recruitment of Yen1 impair its ability to resolve DNA intermediates and result in chromosome mis-segregation and increased genome instability. Public Library of Science 2022-03-25 /pmc/articles/PMC8986097/ /pubmed/35333860 http://dx.doi.org/10.1371/journal.pgen.1009860 Text en © 2022 Dorison et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Dorison, Hugo
Talhaoui, Ibtissam
Mazón, Gerard
SUMO-mediated recruitment allows timely function of the Yen1 nuclease in mitotic cells
title SUMO-mediated recruitment allows timely function of the Yen1 nuclease in mitotic cells
title_full SUMO-mediated recruitment allows timely function of the Yen1 nuclease in mitotic cells
title_fullStr SUMO-mediated recruitment allows timely function of the Yen1 nuclease in mitotic cells
title_full_unstemmed SUMO-mediated recruitment allows timely function of the Yen1 nuclease in mitotic cells
title_short SUMO-mediated recruitment allows timely function of the Yen1 nuclease in mitotic cells
title_sort sumo-mediated recruitment allows timely function of the yen1 nuclease in mitotic cells
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8986097/
https://www.ncbi.nlm.nih.gov/pubmed/35333860
http://dx.doi.org/10.1371/journal.pgen.1009860
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