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Mammalian Base Excision Repair: the Forgotten Archangel
Base excision repair (BER) is a frontline repair system that is responsible for maintaining genome integrity and thus preventing premature aging, cancer and many other human diseases by repairing thousands of DNA lesions and strand breaks continuously caused by endogenous and exogenous mutagens. Thi...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3616742/ https://www.ncbi.nlm.nih.gov/pubmed/23408852 http://dx.doi.org/10.1093/nar/gkt076 |
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author | Dianov, Grigory L. Hübscher, Ulrich |
author_facet | Dianov, Grigory L. Hübscher, Ulrich |
author_sort | Dianov, Grigory L. |
collection | PubMed |
description | Base excision repair (BER) is a frontline repair system that is responsible for maintaining genome integrity and thus preventing premature aging, cancer and many other human diseases by repairing thousands of DNA lesions and strand breaks continuously caused by endogenous and exogenous mutagens. This fundamental and essential function of BER not only necessitates tight control of the continuous availability of basic components for fast and accurate repair, but also requires temporal and spatial coordination of BER and cell cycle progression to prevent replication of damaged DNA. The major goal of this review is to critically examine controversial and newly emerging questions about mammalian BER pathways, mechanisms regulating BER capacity, BER responses to DNA damage and their links to checkpoint control of DNA replication. |
format | Online Article Text |
id | pubmed-3616742 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-36167422013-04-04 Mammalian Base Excision Repair: the Forgotten Archangel Dianov, Grigory L. Hübscher, Ulrich Nucleic Acids Res Survey and Summary Base excision repair (BER) is a frontline repair system that is responsible for maintaining genome integrity and thus preventing premature aging, cancer and many other human diseases by repairing thousands of DNA lesions and strand breaks continuously caused by endogenous and exogenous mutagens. This fundamental and essential function of BER not only necessitates tight control of the continuous availability of basic components for fast and accurate repair, but also requires temporal and spatial coordination of BER and cell cycle progression to prevent replication of damaged DNA. The major goal of this review is to critically examine controversial and newly emerging questions about mammalian BER pathways, mechanisms regulating BER capacity, BER responses to DNA damage and their links to checkpoint control of DNA replication. Oxford University Press 2013-04 2013-02-12 /pmc/articles/PMC3616742/ /pubmed/23408852 http://dx.doi.org/10.1093/nar/gkt076 Text en © The Author(s) 2013. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Survey and Summary Dianov, Grigory L. Hübscher, Ulrich Mammalian Base Excision Repair: the Forgotten Archangel |
title | Mammalian Base Excision Repair: the Forgotten Archangel |
title_full | Mammalian Base Excision Repair: the Forgotten Archangel |
title_fullStr | Mammalian Base Excision Repair: the Forgotten Archangel |
title_full_unstemmed | Mammalian Base Excision Repair: the Forgotten Archangel |
title_short | Mammalian Base Excision Repair: the Forgotten Archangel |
title_sort | mammalian base excision repair: the forgotten archangel |
topic | Survey and Summary |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3616742/ https://www.ncbi.nlm.nih.gov/pubmed/23408852 http://dx.doi.org/10.1093/nar/gkt076 |
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