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Non-equilibrium structural dynamics of supercoiled DNA plasmids exhibits asymmetrical relaxation
Many cellular processes occur out of equilibrium. This includes site-specific unwinding in supercoiled DNA, which may play an important role in gene regulation. Here, we use the Convex Lens-induced Confinement (CLiC) single-molecule microscopy platform to study these processes with high-throughput a...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8934633/ https://www.ncbi.nlm.nih.gov/pubmed/35188541 http://dx.doi.org/10.1093/nar/gkac101 |
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author | Shaheen, Cynthia Hastie, Cameron Metera, Kimberly Scott, Shane Zhang, Zhi Chen, Sitong Gu, Gracia Weber, Lisa Munsky, Brian Kouzine, Fedor Levens, David Benham, Craig Leslie, Sabrina |
author_facet | Shaheen, Cynthia Hastie, Cameron Metera, Kimberly Scott, Shane Zhang, Zhi Chen, Sitong Gu, Gracia Weber, Lisa Munsky, Brian Kouzine, Fedor Levens, David Benham, Craig Leslie, Sabrina |
author_sort | Shaheen, Cynthia |
collection | PubMed |
description | Many cellular processes occur out of equilibrium. This includes site-specific unwinding in supercoiled DNA, which may play an important role in gene regulation. Here, we use the Convex Lens-induced Confinement (CLiC) single-molecule microscopy platform to study these processes with high-throughput and without artificial constraints on molecular structures or interactions. We use two model DNA plasmid systems, pFLIP-FUSE and pUC19, to study the dynamics of supercoiling-induced secondary structural transitions after perturbations away from equilibrium. We find that structural transitions can be slow, leading to long-lived structural states whose kinetics depend on the duration and direction of perturbation. Our findings highlight the importance of out-of-equilibrium studies when characterizing the complex structural dynamics of DNA and understanding the mechanisms of gene regulation. |
format | Online Article Text |
id | pubmed-8934633 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-89346332022-03-21 Non-equilibrium structural dynamics of supercoiled DNA plasmids exhibits asymmetrical relaxation Shaheen, Cynthia Hastie, Cameron Metera, Kimberly Scott, Shane Zhang, Zhi Chen, Sitong Gu, Gracia Weber, Lisa Munsky, Brian Kouzine, Fedor Levens, David Benham, Craig Leslie, Sabrina Nucleic Acids Res Molecular Biology Many cellular processes occur out of equilibrium. This includes site-specific unwinding in supercoiled DNA, which may play an important role in gene regulation. Here, we use the Convex Lens-induced Confinement (CLiC) single-molecule microscopy platform to study these processes with high-throughput and without artificial constraints on molecular structures or interactions. We use two model DNA plasmid systems, pFLIP-FUSE and pUC19, to study the dynamics of supercoiling-induced secondary structural transitions after perturbations away from equilibrium. We find that structural transitions can be slow, leading to long-lived structural states whose kinetics depend on the duration and direction of perturbation. Our findings highlight the importance of out-of-equilibrium studies when characterizing the complex structural dynamics of DNA and understanding the mechanisms of gene regulation. Oxford University Press 2022-02-21 /pmc/articles/PMC8934633/ /pubmed/35188541 http://dx.doi.org/10.1093/nar/gkac101 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of Nucleic Acids Research. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Molecular Biology Shaheen, Cynthia Hastie, Cameron Metera, Kimberly Scott, Shane Zhang, Zhi Chen, Sitong Gu, Gracia Weber, Lisa Munsky, Brian Kouzine, Fedor Levens, David Benham, Craig Leslie, Sabrina Non-equilibrium structural dynamics of supercoiled DNA plasmids exhibits asymmetrical relaxation |
title | Non-equilibrium structural dynamics of supercoiled DNA plasmids exhibits asymmetrical relaxation |
title_full | Non-equilibrium structural dynamics of supercoiled DNA plasmids exhibits asymmetrical relaxation |
title_fullStr | Non-equilibrium structural dynamics of supercoiled DNA plasmids exhibits asymmetrical relaxation |
title_full_unstemmed | Non-equilibrium structural dynamics of supercoiled DNA plasmids exhibits asymmetrical relaxation |
title_short | Non-equilibrium structural dynamics of supercoiled DNA plasmids exhibits asymmetrical relaxation |
title_sort | non-equilibrium structural dynamics of supercoiled dna plasmids exhibits asymmetrical relaxation |
topic | Molecular Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8934633/ https://www.ncbi.nlm.nih.gov/pubmed/35188541 http://dx.doi.org/10.1093/nar/gkac101 |
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