Cargando…
Cooperative kinking at distant sites in mechanically stressed DNA
In cells, DNA is routinely subjected to significant levels of bending and twisting. In some cases, such as under physiological levels of supercoiling, DNA can be so highly strained, that it transitions into non-canonical structural conformations that are capable of relieving mechanical stress within...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2011
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3239204/ https://www.ncbi.nlm.nih.gov/pubmed/21917856 http://dx.doi.org/10.1093/nar/gkr666 |
_version_ | 1782219142871384064 |
---|---|
author | Lionberger, Troy A. Demurtas, Davide Witz, Guillaume Dorier, Julien Lillian, Todd Meyhöfer, Edgar Stasiak, Andrzej |
author_facet | Lionberger, Troy A. Demurtas, Davide Witz, Guillaume Dorier, Julien Lillian, Todd Meyhöfer, Edgar Stasiak, Andrzej |
author_sort | Lionberger, Troy A. |
collection | PubMed |
description | In cells, DNA is routinely subjected to significant levels of bending and twisting. In some cases, such as under physiological levels of supercoiling, DNA can be so highly strained, that it transitions into non-canonical structural conformations that are capable of relieving mechanical stress within the template. DNA minicircles offer a robust model system to study stress-induced DNA structures. Using DNA minicircles on the order of 100 bp in size, we have been able to control the bending and torsional stresses within a looped DNA construct. Through a combination of cryo-EM image reconstructions, Bal31 sensitivity assays and Brownian dynamics simulations, we have been able to analyze the effects of biologically relevant underwinding-induced kinks in DNA on the overall shape of DNA minicircles. Our results indicate that strongly underwound DNA minicircles, which mimic the physical behavior of small regulatory DNA loops, minimize their free energy by undergoing sequential, cooperative kinking at two sites that are located about 180° apart along the periphery of the minicircle. This novel form of structural cooperativity in DNA demonstrates that bending strain can localize hyperflexible kinks within the DNA template, which in turn reduces the energetic cost to tightly loop DNA. |
format | Online Article Text |
id | pubmed-3239204 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-32392042011-12-16 Cooperative kinking at distant sites in mechanically stressed DNA Lionberger, Troy A. Demurtas, Davide Witz, Guillaume Dorier, Julien Lillian, Todd Meyhöfer, Edgar Stasiak, Andrzej Nucleic Acids Res Structural Biology In cells, DNA is routinely subjected to significant levels of bending and twisting. In some cases, such as under physiological levels of supercoiling, DNA can be so highly strained, that it transitions into non-canonical structural conformations that are capable of relieving mechanical stress within the template. DNA minicircles offer a robust model system to study stress-induced DNA structures. Using DNA minicircles on the order of 100 bp in size, we have been able to control the bending and torsional stresses within a looped DNA construct. Through a combination of cryo-EM image reconstructions, Bal31 sensitivity assays and Brownian dynamics simulations, we have been able to analyze the effects of biologically relevant underwinding-induced kinks in DNA on the overall shape of DNA minicircles. Our results indicate that strongly underwound DNA minicircles, which mimic the physical behavior of small regulatory DNA loops, minimize their free energy by undergoing sequential, cooperative kinking at two sites that are located about 180° apart along the periphery of the minicircle. This novel form of structural cooperativity in DNA demonstrates that bending strain can localize hyperflexible kinks within the DNA template, which in turn reduces the energetic cost to tightly loop DNA. Oxford University Press 2011-12 2011-09-14 /pmc/articles/PMC3239204/ /pubmed/21917856 http://dx.doi.org/10.1093/nar/gkr666 Text en © The Author(s) 2011. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Structural Biology Lionberger, Troy A. Demurtas, Davide Witz, Guillaume Dorier, Julien Lillian, Todd Meyhöfer, Edgar Stasiak, Andrzej Cooperative kinking at distant sites in mechanically stressed DNA |
title | Cooperative kinking at distant sites in mechanically stressed DNA |
title_full | Cooperative kinking at distant sites in mechanically stressed DNA |
title_fullStr | Cooperative kinking at distant sites in mechanically stressed DNA |
title_full_unstemmed | Cooperative kinking at distant sites in mechanically stressed DNA |
title_short | Cooperative kinking at distant sites in mechanically stressed DNA |
title_sort | cooperative kinking at distant sites in mechanically stressed dna |
topic | Structural Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3239204/ https://www.ncbi.nlm.nih.gov/pubmed/21917856 http://dx.doi.org/10.1093/nar/gkr666 |
work_keys_str_mv | AT lionbergertroya cooperativekinkingatdistantsitesinmechanicallystresseddna AT demurtasdavide cooperativekinkingatdistantsitesinmechanicallystresseddna AT witzguillaume cooperativekinkingatdistantsitesinmechanicallystresseddna AT dorierjulien cooperativekinkingatdistantsitesinmechanicallystresseddna AT lilliantodd cooperativekinkingatdistantsitesinmechanicallystresseddna AT meyhoferedgar cooperativekinkingatdistantsitesinmechanicallystresseddna AT stasiakandrzej cooperativekinkingatdistantsitesinmechanicallystresseddna |