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A failure of meiotic chromosome segregation in a fbh1Δ mutant correlates with persistent Rad51-DNA associations

The F-box DNA helicase Fbh1 constrains homologous recombination in vegetative cells, most likely through an ability to displace the Rad51 recombinase from DNA. Here, we provide the first evidence that Fbh1 also serves a vital meiotic role in fission yeast to promote normal chromosome segregation. In...

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Detalles Bibliográficos
Autores principales: Sun, Weili, Lorenz, Alexander, Osman, Fekret, Whitby, Matthew C.
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3061084/
https://www.ncbi.nlm.nih.gov/pubmed/21149262
http://dx.doi.org/10.1093/nar/gkq977
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author Sun, Weili
Lorenz, Alexander
Osman, Fekret
Whitby, Matthew C.
author_facet Sun, Weili
Lorenz, Alexander
Osman, Fekret
Whitby, Matthew C.
author_sort Sun, Weili
collection PubMed
description The F-box DNA helicase Fbh1 constrains homologous recombination in vegetative cells, most likely through an ability to displace the Rad51 recombinase from DNA. Here, we provide the first evidence that Fbh1 also serves a vital meiotic role in fission yeast to promote normal chromosome segregation. In the absence of Fbh1, chromosomes remain entangled or segregate unevenly during meiosis, and genetic and cytological data suggest that this results in part from a failure to efficiently dismantle Rad51 nucleofilaments that form during meiotic double-strand break repair.
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spelling pubmed-30610842011-03-21 A failure of meiotic chromosome segregation in a fbh1Δ mutant correlates with persistent Rad51-DNA associations Sun, Weili Lorenz, Alexander Osman, Fekret Whitby, Matthew C. Nucleic Acids Res Genome Integrity, Repair and Replication The F-box DNA helicase Fbh1 constrains homologous recombination in vegetative cells, most likely through an ability to displace the Rad51 recombinase from DNA. Here, we provide the first evidence that Fbh1 also serves a vital meiotic role in fission yeast to promote normal chromosome segregation. In the absence of Fbh1, chromosomes remain entangled or segregate unevenly during meiosis, and genetic and cytological data suggest that this results in part from a failure to efficiently dismantle Rad51 nucleofilaments that form during meiotic double-strand break repair. Oxford University Press 2011-03 2010-12-11 /pmc/articles/PMC3061084/ /pubmed/21149262 http://dx.doi.org/10.1093/nar/gkq977 Text en © The Author(s) 2010. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/2.5 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.5), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Genome Integrity, Repair and Replication
Sun, Weili
Lorenz, Alexander
Osman, Fekret
Whitby, Matthew C.
A failure of meiotic chromosome segregation in a fbh1Δ mutant correlates with persistent Rad51-DNA associations
title A failure of meiotic chromosome segregation in a fbh1Δ mutant correlates with persistent Rad51-DNA associations
title_full A failure of meiotic chromosome segregation in a fbh1Δ mutant correlates with persistent Rad51-DNA associations
title_fullStr A failure of meiotic chromosome segregation in a fbh1Δ mutant correlates with persistent Rad51-DNA associations
title_full_unstemmed A failure of meiotic chromosome segregation in a fbh1Δ mutant correlates with persistent Rad51-DNA associations
title_short A failure of meiotic chromosome segregation in a fbh1Δ mutant correlates with persistent Rad51-DNA associations
title_sort failure of meiotic chromosome segregation in a fbh1δ mutant correlates with persistent rad51-dna associations
topic Genome Integrity, Repair and Replication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3061084/
https://www.ncbi.nlm.nih.gov/pubmed/21149262
http://dx.doi.org/10.1093/nar/gkq977
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