Break-induced replication promotes formation of lethal joint molecules dissolved by Srs2

Break-induced replication (BIR) is a double-strand break repair pathway that can lead to genomic instability. Here the authors show that the absence of Srs2 helicase during BIR leads to uncontrolled binding of Rad51 to single-stranded DNA, which promotes the formation of toxic intermediates that nee...

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Autores principales: Rajula Elango, Ziwei Sheng, Jessica Jackson, Jenna DeCata, Younis Ibrahim, Nhung T. Pham, Diana H. Liang, Cynthia J. Sakofsky, Alessandro Vindigni, Kirill S. Lobachev, Grzegorz Ira, Anna Malkova
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Lenguaje:EN
Publicado: Nature Portfolio 2017
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Acceso en línea:https://doaj.org/article/9b329335ec744672ad3e5e67091d04d5
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spelling oai:doaj.org-article:9b329335ec744672ad3e5e67091d04d52021-12-02T14:40:23ZBreak-induced replication promotes formation of lethal joint molecules dissolved by Srs210.1038/s41467-017-01987-22041-1723https://doaj.org/article/9b329335ec744672ad3e5e67091d04d52017-11-01T00:00:00Zhttps://doi.org/10.1038/s41467-017-01987-2https://doaj.org/toc/2041-1723Break-induced replication (BIR) is a double-strand break repair pathway that can lead to genomic instability. Here the authors show that the absence of Srs2 helicase during BIR leads to uncontrolled binding of Rad51 to single-stranded DNA, which promotes the formation of toxic intermediates that need to be resolved by Mus81 or Yen1.Rajula ElangoZiwei ShengJessica JacksonJenna DeCataYounis IbrahimNhung T. PhamDiana H. LiangCynthia J. SakofskyAlessandro VindigniKirill S. LobachevGrzegorz IraAnna MalkovaNature PortfolioarticleScienceQENNature Communications, Vol 8, Iss 1, Pp 1-13 (2017)
institution DOAJ
collection DOAJ
language EN
topic Science
Q
spellingShingle Science
Q
Rajula Elango
Ziwei Sheng
Jessica Jackson
Jenna DeCata
Younis Ibrahim
Nhung T. Pham
Diana H. Liang
Cynthia J. Sakofsky
Alessandro Vindigni
Kirill S. Lobachev
Grzegorz Ira
Anna Malkova
Break-induced replication promotes formation of lethal joint molecules dissolved by Srs2
description Break-induced replication (BIR) is a double-strand break repair pathway that can lead to genomic instability. Here the authors show that the absence of Srs2 helicase during BIR leads to uncontrolled binding of Rad51 to single-stranded DNA, which promotes the formation of toxic intermediates that need to be resolved by Mus81 or Yen1.
format article
author Rajula Elango
Ziwei Sheng
Jessica Jackson
Jenna DeCata
Younis Ibrahim
Nhung T. Pham
Diana H. Liang
Cynthia J. Sakofsky
Alessandro Vindigni
Kirill S. Lobachev
Grzegorz Ira
Anna Malkova
author_facet Rajula Elango
Ziwei Sheng
Jessica Jackson
Jenna DeCata
Younis Ibrahim
Nhung T. Pham
Diana H. Liang
Cynthia J. Sakofsky
Alessandro Vindigni
Kirill S. Lobachev
Grzegorz Ira
Anna Malkova
author_sort Rajula Elango
title Break-induced replication promotes formation of lethal joint molecules dissolved by Srs2
title_short Break-induced replication promotes formation of lethal joint molecules dissolved by Srs2
title_full Break-induced replication promotes formation of lethal joint molecules dissolved by Srs2
title_fullStr Break-induced replication promotes formation of lethal joint molecules dissolved by Srs2
title_full_unstemmed Break-induced replication promotes formation of lethal joint molecules dissolved by Srs2
title_sort break-induced replication promotes formation of lethal joint molecules dissolved by srs2
publisher Nature Portfolio
publishDate 2017
url https://doaj.org/article/9b329335ec744672ad3e5e67091d04d5
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