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In the absence of writhe, DNA relieves torsional stress with localized, sequence-dependent structural failure to preserve B-form

To understand how underwinding and overwinding the DNA helix affects its structure, we simulated 19 independent DNA systems with fixed degrees of twist using molecular dynamics in a system that does not allow writhe. Underwinding DNA induced spontaneous, sequence-dependent base flipping and local de...

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Detalles Bibliográficos
Autores principales: Randall, Graham L., Zechiedrich, Lynn, Pettitt, B. Montgomery
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2760789/
https://www.ncbi.nlm.nih.gov/pubmed/19586933
http://dx.doi.org/10.1093/nar/gkp556
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author Randall, Graham L.
Zechiedrich, Lynn
Pettitt, B. Montgomery
author_facet Randall, Graham L.
Zechiedrich, Lynn
Pettitt, B. Montgomery
author_sort Randall, Graham L.
collection PubMed
description To understand how underwinding and overwinding the DNA helix affects its structure, we simulated 19 independent DNA systems with fixed degrees of twist using molecular dynamics in a system that does not allow writhe. Underwinding DNA induced spontaneous, sequence-dependent base flipping and local denaturation, while overwinding DNA induced the formation of Pauling-like DNA (P-DNA). The winding resulted in a bimodal state simultaneously including local structural failure and B-form DNA for both underwinding and extreme overwinding. Our simulations suggest that base flipping and local denaturation may provide a landscape influencing protein recognition of DNA sequence to affect, for examples, replication, transcription and recombination. Additionally, our findings help explain results from single-molecule experiments and demonstrate that elastic rod models are strictly valid on average only for unstressed or overwound DNA up to P-DNA formation. Finally, our data support a model in which base flipping can result from torsional stress.
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spelling pubmed-27607892009-10-13 In the absence of writhe, DNA relieves torsional stress with localized, sequence-dependent structural failure to preserve B-form Randall, Graham L. Zechiedrich, Lynn Pettitt, B. Montgomery Nucleic Acids Res Structural Biology To understand how underwinding and overwinding the DNA helix affects its structure, we simulated 19 independent DNA systems with fixed degrees of twist using molecular dynamics in a system that does not allow writhe. Underwinding DNA induced spontaneous, sequence-dependent base flipping and local denaturation, while overwinding DNA induced the formation of Pauling-like DNA (P-DNA). The winding resulted in a bimodal state simultaneously including local structural failure and B-form DNA for both underwinding and extreme overwinding. Our simulations suggest that base flipping and local denaturation may provide a landscape influencing protein recognition of DNA sequence to affect, for examples, replication, transcription and recombination. Additionally, our findings help explain results from single-molecule experiments and demonstrate that elastic rod models are strictly valid on average only for unstressed or overwound DNA up to P-DNA formation. Finally, our data support a model in which base flipping can result from torsional stress. Oxford University Press 2009-09 2009-07-08 /pmc/articles/PMC2760789/ /pubmed/19586933 http://dx.doi.org/10.1093/nar/gkp556 Text en © 2009 The Author(s) http://creativecommons.org/licenses/by-nc/2.0/uk/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.0/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Structural Biology
Randall, Graham L.
Zechiedrich, Lynn
Pettitt, B. Montgomery
In the absence of writhe, DNA relieves torsional stress with localized, sequence-dependent structural failure to preserve B-form
title In the absence of writhe, DNA relieves torsional stress with localized, sequence-dependent structural failure to preserve B-form
title_full In the absence of writhe, DNA relieves torsional stress with localized, sequence-dependent structural failure to preserve B-form
title_fullStr In the absence of writhe, DNA relieves torsional stress with localized, sequence-dependent structural failure to preserve B-form
title_full_unstemmed In the absence of writhe, DNA relieves torsional stress with localized, sequence-dependent structural failure to preserve B-form
title_short In the absence of writhe, DNA relieves torsional stress with localized, sequence-dependent structural failure to preserve B-form
title_sort in the absence of writhe, dna relieves torsional stress with localized, sequence-dependent structural failure to preserve b-form
topic Structural Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2760789/
https://www.ncbi.nlm.nih.gov/pubmed/19586933
http://dx.doi.org/10.1093/nar/gkp556
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