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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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Formato: | Texto |
Lenguaje: | English |
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Oxford University Press
2009
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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. |
format | Text |
id | pubmed-2760789 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
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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