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Pathway choice in DNA double strand break repair: observations of a balancing act

Proper repair of DNA double strand breaks (DSBs) is vital for the preservation of genomic integrity. There are two main pathways that repair DSBs, Homologous recombination (HR) and Non-homologous end-joining (NHEJ). HR is restricted to the S and G2 phases of the cell cycle due to the requirement for...

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Detalles Bibliográficos
Autores principales: Brandsma, Inger, Gent, Dik C
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3557175/
https://www.ncbi.nlm.nih.gov/pubmed/23181949
http://dx.doi.org/10.1186/2041-9414-3-9
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author Brandsma, Inger
Gent, Dik C
author_facet Brandsma, Inger
Gent, Dik C
author_sort Brandsma, Inger
collection PubMed
description Proper repair of DNA double strand breaks (DSBs) is vital for the preservation of genomic integrity. There are two main pathways that repair DSBs, Homologous recombination (HR) and Non-homologous end-joining (NHEJ). HR is restricted to the S and G2 phases of the cell cycle due to the requirement for the sister chromatid as a template, while NHEJ is active throughout the cell cycle and does not rely on a template. The balance between both pathways is essential for genome stability and numerous assays have been developed to measure the efficiency of the two pathways. Several proteins are known to affect the balance between HR and NHEJ and the complexity of the break also plays a role. In this review we describe several repair assays to determine the efficiencies of both pathways. We discuss how disturbance of the balance between HR and NHEJ can lead to disease, but also how it can be exploited for cancer treatment.
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spelling pubmed-35571752013-01-31 Pathway choice in DNA double strand break repair: observations of a balancing act Brandsma, Inger Gent, Dik C Genome Integr Review Proper repair of DNA double strand breaks (DSBs) is vital for the preservation of genomic integrity. There are two main pathways that repair DSBs, Homologous recombination (HR) and Non-homologous end-joining (NHEJ). HR is restricted to the S and G2 phases of the cell cycle due to the requirement for the sister chromatid as a template, while NHEJ is active throughout the cell cycle and does not rely on a template. The balance between both pathways is essential for genome stability and numerous assays have been developed to measure the efficiency of the two pathways. Several proteins are known to affect the balance between HR and NHEJ and the complexity of the break also plays a role. In this review we describe several repair assays to determine the efficiencies of both pathways. We discuss how disturbance of the balance between HR and NHEJ can lead to disease, but also how it can be exploited for cancer treatment. BioMed Central 2012-11-27 /pmc/articles/PMC3557175/ /pubmed/23181949 http://dx.doi.org/10.1186/2041-9414-3-9 Text en Copyright ©2012 Brandsma and van Gent; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
Brandsma, Inger
Gent, Dik C
Pathway choice in DNA double strand break repair: observations of a balancing act
title Pathway choice in DNA double strand break repair: observations of a balancing act
title_full Pathway choice in DNA double strand break repair: observations of a balancing act
title_fullStr Pathway choice in DNA double strand break repair: observations of a balancing act
title_full_unstemmed Pathway choice in DNA double strand break repair: observations of a balancing act
title_short Pathway choice in DNA double strand break repair: observations of a balancing act
title_sort pathway choice in dna double strand break repair: observations of a balancing act
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3557175/
https://www.ncbi.nlm.nih.gov/pubmed/23181949
http://dx.doi.org/10.1186/2041-9414-3-9
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