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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...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
AIMS Press
2019
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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 |
author_sort | Son, Mi Young |
collection | PubMed |
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. |
format | Online Article Text |
id | pubmed-6690234 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | AIMS Press |
record_format | MEDLINE/PubMed |
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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