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Structural diversity of supercoiled DNA
By regulating access to the genetic code, DNA supercoiling strongly affects DNA metabolism. Despite its importance, however, much about supercoiled DNA (positively supercoiled DNA, in particular) remains unknown. Here we use electron cryo-tomography together with biochemical analyses to investigate...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Pub. Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4608029/ https://www.ncbi.nlm.nih.gov/pubmed/26455586 http://dx.doi.org/10.1038/ncomms9440 |
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author | Irobalieva, Rossitza N. Fogg, Jonathan M. Catanese, Daniel J. Sutthibutpong, Thana Chen, Muyuan Barker, Anna K. Ludtke, Steven J. Harris, Sarah A. Schmid, Michael F. Chiu, Wah Zechiedrich, Lynn |
author_facet | Irobalieva, Rossitza N. Fogg, Jonathan M. Catanese, Daniel J. Sutthibutpong, Thana Chen, Muyuan Barker, Anna K. Ludtke, Steven J. Harris, Sarah A. Schmid, Michael F. Chiu, Wah Zechiedrich, Lynn |
author_sort | Irobalieva, Rossitza N. |
collection | PubMed |
description | By regulating access to the genetic code, DNA supercoiling strongly affects DNA metabolism. Despite its importance, however, much about supercoiled DNA (positively supercoiled DNA, in particular) remains unknown. Here we use electron cryo-tomography together with biochemical analyses to investigate structures of individual purified DNA minicircle topoisomers with defined degrees of supercoiling. Our results reveal that each topoisomer, negative or positive, adopts a unique and surprisingly wide distribution of three-dimensional conformations. Moreover, we uncover striking differences in how the topoisomers handle torsional stress. As negative supercoiling increases, bases are increasingly exposed. Beyond a sharp supercoiling threshold, we also detect exposed bases in positively supercoiled DNA. Molecular dynamics simulations independently confirm the conformational heterogeneity and provide atomistic insight into the flexibility of supercoiled DNA. Our integrated approach reveals the three-dimensional structures of DNA that are essential for its function. |
format | Online Article Text |
id | pubmed-4608029 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Pub. Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-46080292015-11-25 Structural diversity of supercoiled DNA Irobalieva, Rossitza N. Fogg, Jonathan M. Catanese, Daniel J. Sutthibutpong, Thana Chen, Muyuan Barker, Anna K. Ludtke, Steven J. Harris, Sarah A. Schmid, Michael F. Chiu, Wah Zechiedrich, Lynn Nat Commun Article By regulating access to the genetic code, DNA supercoiling strongly affects DNA metabolism. Despite its importance, however, much about supercoiled DNA (positively supercoiled DNA, in particular) remains unknown. Here we use electron cryo-tomography together with biochemical analyses to investigate structures of individual purified DNA minicircle topoisomers with defined degrees of supercoiling. Our results reveal that each topoisomer, negative or positive, adopts a unique and surprisingly wide distribution of three-dimensional conformations. Moreover, we uncover striking differences in how the topoisomers handle torsional stress. As negative supercoiling increases, bases are increasingly exposed. Beyond a sharp supercoiling threshold, we also detect exposed bases in positively supercoiled DNA. Molecular dynamics simulations independently confirm the conformational heterogeneity and provide atomistic insight into the flexibility of supercoiled DNA. Our integrated approach reveals the three-dimensional structures of DNA that are essential for its function. Nature Pub. Group 2015-10-12 /pmc/articles/PMC4608029/ /pubmed/26455586 http://dx.doi.org/10.1038/ncomms9440 Text en Copyright © 2015, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Irobalieva, Rossitza N. Fogg, Jonathan M. Catanese, Daniel J. Sutthibutpong, Thana Chen, Muyuan Barker, Anna K. Ludtke, Steven J. Harris, Sarah A. Schmid, Michael F. Chiu, Wah Zechiedrich, Lynn Structural diversity of supercoiled DNA |
title | Structural diversity of supercoiled DNA |
title_full | Structural diversity of supercoiled DNA |
title_fullStr | Structural diversity of supercoiled DNA |
title_full_unstemmed | Structural diversity of supercoiled DNA |
title_short | Structural diversity of supercoiled DNA |
title_sort | structural diversity of supercoiled dna |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4608029/ https://www.ncbi.nlm.nih.gov/pubmed/26455586 http://dx.doi.org/10.1038/ncomms9440 |
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