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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...

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Autores principales: Lim, Wilber, Randisi, Ferdinando, Doye, Jonathan P K, Louis, Ard A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
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.
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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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