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Homologous recombination defects and how they affect replication fork maintenance

Homologous recombination (HR) repairs DNA double strand breaks (DSBs) and stabilizes replication forks (RFs). RAD51 is the recombinase for the HR pathway. To preserve genomic integrity, RAD51 forms a filament on the 3′ end of a DSB and on a single-stranded DNA (ssDNA) gap. But unregulated HR results...

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Detalles Bibliográficos
Autores principales: Son, Mi Young, Hasty, Paul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AIMS Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6690234/
https://www.ncbi.nlm.nih.gov/pubmed/31435521
http://dx.doi.org/10.3934/genet.2018.4.192
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author Son, Mi Young
Hasty, Paul
author_facet Son, Mi Young
Hasty, Paul
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description Homologous recombination (HR) repairs DNA double strand breaks (DSBs) and stabilizes replication forks (RFs). RAD51 is the recombinase for the HR pathway. To preserve genomic integrity, RAD51 forms a filament on the 3′ end of a DSB and on a single-stranded DNA (ssDNA) gap. But unregulated HR results in undesirable chromosomal rearrangements. This review describes the multiple mechanisms that regulate HR with a focus on those mechanisms that promote and contain RAD51 filaments to limit chromosomal rearrangements. If any of these pathways break down and HR becomes unregulated then disease, primarily cancer, can result.
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spelling pubmed-66902342019-08-21 Homologous recombination defects and how they affect replication fork maintenance Son, Mi Young Hasty, Paul AIMS Genet Review Homologous recombination (HR) repairs DNA double strand breaks (DSBs) and stabilizes replication forks (RFs). RAD51 is the recombinase for the HR pathway. To preserve genomic integrity, RAD51 forms a filament on the 3′ end of a DSB and on a single-stranded DNA (ssDNA) gap. But unregulated HR results in undesirable chromosomal rearrangements. This review describes the multiple mechanisms that regulate HR with a focus on those mechanisms that promote and contain RAD51 filaments to limit chromosomal rearrangements. If any of these pathways break down and HR becomes unregulated then disease, primarily cancer, can result. AIMS Press 2019-04-03 /pmc/articles/PMC6690234/ /pubmed/31435521 http://dx.doi.org/10.3934/genet.2018.4.192 Text en © 2018 the Author(s), licensee AIMS Press This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0)
spellingShingle Review
Son, Mi Young
Hasty, Paul
Homologous recombination defects and how they affect replication fork maintenance
title Homologous recombination defects and how they affect replication fork maintenance
title_full Homologous recombination defects and how they affect replication fork maintenance
title_fullStr Homologous recombination defects and how they affect replication fork maintenance
title_full_unstemmed Homologous recombination defects and how they affect replication fork maintenance
title_short Homologous recombination defects and how they affect replication fork maintenance
title_sort homologous recombination defects and how they affect replication fork maintenance
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6690234/
https://www.ncbi.nlm.nih.gov/pubmed/31435521
http://dx.doi.org/10.3934/genet.2018.4.192
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