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A Mathematical Model for DNA Damage and Repair

In cells, DNA repair has to keep up with DNA damage to maintain the integrity of the genome and prevent mutagenesis and carcinogenesis. While the importance of both DNA damage and repair is clear, the impact of imbalances between both processes has not been studied. In this paper, we created a combi...

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Detalles Bibliográficos
Autores principales: Crooke, Philip S., Parl, Fritz F.
Formato: Texto
Lenguaje:English
Publicado: SAGE-Hindawi Access to Research 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2915813/
https://www.ncbi.nlm.nih.gov/pubmed/20725623
http://dx.doi.org/10.4061/2010/352603
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author Crooke, Philip S.
Parl, Fritz F.
author_facet Crooke, Philip S.
Parl, Fritz F.
author_sort Crooke, Philip S.
collection PubMed
description In cells, DNA repair has to keep up with DNA damage to maintain the integrity of the genome and prevent mutagenesis and carcinogenesis. While the importance of both DNA damage and repair is clear, the impact of imbalances between both processes has not been studied. In this paper, we created a combined mathematical model for the formation of DNA adducts from oxidative estrogen metabolism followed by base excision repair (BER) of these adducts. The model encompasses a set of differential equations representing the sequence of enzymatic reactions in both damage and repair pathways. By combining both pathways, we can simulate the overall process by starting from a given time-dependent concentration of 17β-estradiol (E(2)) and 2′-deoxyguanosine, determine the extent of adduct formation and the correction by BER required to preserve the integrity of DNA. The model allows us to examine the effect of phenotypic and genotypic factors such as different concentrations of estrogen and variant enzyme haplotypes on the formation and repair of DNA adducts.
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spelling pubmed-29158132010-08-19 A Mathematical Model for DNA Damage and Repair Crooke, Philip S. Parl, Fritz F. J Nucleic Acids Research Article In cells, DNA repair has to keep up with DNA damage to maintain the integrity of the genome and prevent mutagenesis and carcinogenesis. While the importance of both DNA damage and repair is clear, the impact of imbalances between both processes has not been studied. In this paper, we created a combined mathematical model for the formation of DNA adducts from oxidative estrogen metabolism followed by base excision repair (BER) of these adducts. The model encompasses a set of differential equations representing the sequence of enzymatic reactions in both damage and repair pathways. By combining both pathways, we can simulate the overall process by starting from a given time-dependent concentration of 17β-estradiol (E(2)) and 2′-deoxyguanosine, determine the extent of adduct formation and the correction by BER required to preserve the integrity of DNA. The model allows us to examine the effect of phenotypic and genotypic factors such as different concentrations of estrogen and variant enzyme haplotypes on the formation and repair of DNA adducts. SAGE-Hindawi Access to Research 2010-07-25 /pmc/articles/PMC2915813/ /pubmed/20725623 http://dx.doi.org/10.4061/2010/352603 Text en Copyright © 2010 P. S. Crooke and F. F. Parl. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Crooke, Philip S.
Parl, Fritz F.
A Mathematical Model for DNA Damage and Repair
title A Mathematical Model for DNA Damage and Repair
title_full A Mathematical Model for DNA Damage and Repair
title_fullStr A Mathematical Model for DNA Damage and Repair
title_full_unstemmed A Mathematical Model for DNA Damage and Repair
title_short A Mathematical Model for DNA Damage and Repair
title_sort mathematical model for dna damage and repair
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2915813/
https://www.ncbi.nlm.nih.gov/pubmed/20725623
http://dx.doi.org/10.4061/2010/352603
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