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The interplay of supercoiling and thymine dimers in DNA
Thymine dimers are a major mutagenic photoproduct induced by UV radiation. While they have been the subject of extensive theoretical and experimental investigations, questions of how DNA supercoiling affects local defect properties, or, conversely, how the presence of such defects changes global sup...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8934635/ https://www.ncbi.nlm.nih.gov/pubmed/35188542 http://dx.doi.org/10.1093/nar/gkac082 |
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author | Lim, Wilber Randisi, Ferdinando Doye, Jonathan P K Louis, Ard A |
author_facet | Lim, Wilber Randisi, Ferdinando Doye, Jonathan P K Louis, Ard A |
author_sort | Lim, Wilber |
collection | PubMed |
description | Thymine dimers are a major mutagenic photoproduct induced by UV radiation. While they have been the subject of extensive theoretical and experimental investigations, questions of how DNA supercoiling affects local defect properties, or, conversely, how the presence of such defects changes global supercoiled structure, are largely unexplored. Here, we introduce a model of thymine dimers in the oxDNA forcefield, parametrized by comparison to melting experiments and structural measurements of the thymine dimer induced bend angle. We performed extensive molecular dynamics simulations of double-stranded DNA as a function of external twist and force. Compared to undamaged DNA, the presence of a thymine dimer lowers the supercoiling densities at which plectonemes and bubbles occur. For biologically relevant supercoiling densities and forces, thymine dimers can preferentially segregate to the tips of the plectonemes, where they enhance the probability of a localized tip-bubble. This mechanism increases the probability of highly bent and denatured states at the thymine dimer site, which may facilitate repair enzyme binding. Thymine dimer-induced tip-bubbles also pin plectonemes, which may help repair enzymes to locate damage. We hypothesize that the interplay of supercoiling and local defects plays an important role for a wider set of DNA damage repair systems. |
format | Online Article Text |
id | pubmed-8934635 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-89346352022-03-21 The interplay of supercoiling and thymine dimers in DNA Lim, Wilber Randisi, Ferdinando Doye, Jonathan P K Louis, Ard A Nucleic Acids Res Computational Biology Thymine dimers are a major mutagenic photoproduct induced by UV radiation. While they have been the subject of extensive theoretical and experimental investigations, questions of how DNA supercoiling affects local defect properties, or, conversely, how the presence of such defects changes global supercoiled structure, are largely unexplored. Here, we introduce a model of thymine dimers in the oxDNA forcefield, parametrized by comparison to melting experiments and structural measurements of the thymine dimer induced bend angle. We performed extensive molecular dynamics simulations of double-stranded DNA as a function of external twist and force. Compared to undamaged DNA, the presence of a thymine dimer lowers the supercoiling densities at which plectonemes and bubbles occur. For biologically relevant supercoiling densities and forces, thymine dimers can preferentially segregate to the tips of the plectonemes, where they enhance the probability of a localized tip-bubble. This mechanism increases the probability of highly bent and denatured states at the thymine dimer site, which may facilitate repair enzyme binding. Thymine dimer-induced tip-bubbles also pin plectonemes, which may help repair enzymes to locate damage. We hypothesize that the interplay of supercoiling and local defects plays an important role for a wider set of DNA damage repair systems. Oxford University Press 2022-02-21 /pmc/articles/PMC8934635/ /pubmed/35188542 http://dx.doi.org/10.1093/nar/gkac082 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of Nucleic Acids Research. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Computational Biology Lim, Wilber Randisi, Ferdinando Doye, Jonathan P K Louis, Ard A The interplay of supercoiling and thymine dimers in DNA |
title | The interplay of supercoiling and thymine dimers in DNA |
title_full | The interplay of supercoiling and thymine dimers in DNA |
title_fullStr | The interplay of supercoiling and thymine dimers in DNA |
title_full_unstemmed | The interplay of supercoiling and thymine dimers in DNA |
title_short | The interplay of supercoiling and thymine dimers in DNA |
title_sort | interplay of supercoiling and thymine dimers in dna |
topic | Computational Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8934635/ https://www.ncbi.nlm.nih.gov/pubmed/35188542 http://dx.doi.org/10.1093/nar/gkac082 |
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