Cargando…
A biomechanical mechanism for initiating DNA packaging
The bacterial chromosome is under varying levels of mechanical stress due to a high degree of crowding and dynamic protein–DNA interactions experienced within the nucleoid. DNA tension is difficult to measure in cells and its functional significance remains unclear although in vitro experiments have...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4231757/ https://www.ncbi.nlm.nih.gov/pubmed/25274732 http://dx.doi.org/10.1093/nar/gku896 |
_version_ | 1782344482133377024 |
---|---|
author | Wang, Haowei Yehoshua, Samuel Ali, Sabrina S. Navarre, William Wiley Milstein, Joshua N. |
author_facet | Wang, Haowei Yehoshua, Samuel Ali, Sabrina S. Navarre, William Wiley Milstein, Joshua N. |
author_sort | Wang, Haowei |
collection | PubMed |
description | The bacterial chromosome is under varying levels of mechanical stress due to a high degree of crowding and dynamic protein–DNA interactions experienced within the nucleoid. DNA tension is difficult to measure in cells and its functional significance remains unclear although in vitro experiments have implicated a range of biomechanical phenomena. Using single-molecule tools, we have uncovered a novel protein–DNA interaction that responds to fluctuations in mechanical tension by condensing DNA. We combined tethered particle motion (TPM) and optical tweezers experiments to probe the effects of tension on DNA in the presence of the Hha/H-NS complex. The nucleoid structuring protein H-NS is a key regulator of DNA condensation and gene expression in enterobacteria and its activity in vivo is affected by the accessory factor Hha. We find that tension, induced by optical tweezers, causes the rapid compaction of DNA in the presence of the Hha/H-NS complex, but not in the presence of H-NS alone. Our results imply that H-NS requires Hha to condense bacterial DNA and that this condensation could be triggered by the level of mechanical tension experienced along different regions of the chromosome. |
format | Online Article Text |
id | pubmed-4231757 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-42317572014-11-21 A biomechanical mechanism for initiating DNA packaging Wang, Haowei Yehoshua, Samuel Ali, Sabrina S. Navarre, William Wiley Milstein, Joshua N. Nucleic Acids Res Gene regulation, Chromatin and Epigenetics The bacterial chromosome is under varying levels of mechanical stress due to a high degree of crowding and dynamic protein–DNA interactions experienced within the nucleoid. DNA tension is difficult to measure in cells and its functional significance remains unclear although in vitro experiments have implicated a range of biomechanical phenomena. Using single-molecule tools, we have uncovered a novel protein–DNA interaction that responds to fluctuations in mechanical tension by condensing DNA. We combined tethered particle motion (TPM) and optical tweezers experiments to probe the effects of tension on DNA in the presence of the Hha/H-NS complex. The nucleoid structuring protein H-NS is a key regulator of DNA condensation and gene expression in enterobacteria and its activity in vivo is affected by the accessory factor Hha. We find that tension, induced by optical tweezers, causes the rapid compaction of DNA in the presence of the Hha/H-NS complex, but not in the presence of H-NS alone. Our results imply that H-NS requires Hha to condense bacterial DNA and that this condensation could be triggered by the level of mechanical tension experienced along different regions of the chromosome. Oxford University Press 2014-10-29 2014-10-01 /pmc/articles/PMC4231757/ /pubmed/25274732 http://dx.doi.org/10.1093/nar/gku896 Text en © The Author(s) 2014. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Gene regulation, Chromatin and Epigenetics Wang, Haowei Yehoshua, Samuel Ali, Sabrina S. Navarre, William Wiley Milstein, Joshua N. A biomechanical mechanism for initiating DNA packaging |
title | A biomechanical mechanism for initiating DNA packaging |
title_full | A biomechanical mechanism for initiating DNA packaging |
title_fullStr | A biomechanical mechanism for initiating DNA packaging |
title_full_unstemmed | A biomechanical mechanism for initiating DNA packaging |
title_short | A biomechanical mechanism for initiating DNA packaging |
title_sort | biomechanical mechanism for initiating dna packaging |
topic | Gene regulation, Chromatin and Epigenetics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4231757/ https://www.ncbi.nlm.nih.gov/pubmed/25274732 http://dx.doi.org/10.1093/nar/gku896 |
work_keys_str_mv | AT wanghaowei abiomechanicalmechanismforinitiatingdnapackaging AT yehoshuasamuel abiomechanicalmechanismforinitiatingdnapackaging AT alisabrinas abiomechanicalmechanismforinitiatingdnapackaging AT navarrewilliamwiley abiomechanicalmechanismforinitiatingdnapackaging AT milsteinjoshuan abiomechanicalmechanismforinitiatingdnapackaging AT wanghaowei biomechanicalmechanismforinitiatingdnapackaging AT yehoshuasamuel biomechanicalmechanismforinitiatingdnapackaging AT alisabrinas biomechanicalmechanismforinitiatingdnapackaging AT navarrewilliamwiley biomechanicalmechanismforinitiatingdnapackaging AT milsteinjoshuan biomechanicalmechanismforinitiatingdnapackaging |