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Spatial confinement induces hairpins in nicked circular DNA
In living cells, DNA is highly confined in space with the help of condensing agents, DNA binding proteins and high levels of supercoiling. Due to challenges associated with experimentally studying DNA under confinement, little is known about the impact of spatial confinement on the local structure o...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5605231/ https://www.ncbi.nlm.nih.gov/pubmed/28201616 http://dx.doi.org/10.1093/nar/gkx098 |
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author | Japaridze, Aleksandre Orlandini, Enzo Smith, Kathleen Beth Gmür, Lucas Valle, Francesco Micheletti, Cristian Dietler, Giovanni |
author_facet | Japaridze, Aleksandre Orlandini, Enzo Smith, Kathleen Beth Gmür, Lucas Valle, Francesco Micheletti, Cristian Dietler, Giovanni |
author_sort | Japaridze, Aleksandre |
collection | PubMed |
description | In living cells, DNA is highly confined in space with the help of condensing agents, DNA binding proteins and high levels of supercoiling. Due to challenges associated with experimentally studying DNA under confinement, little is known about the impact of spatial confinement on the local structure of the DNA. Here, we have used well characterized slits of different sizes to collect high resolution atomic force microscopy images of confined circular DNA with the aim of assessing the impact of the spatial confinement on global and local conformational properties of DNA. Our findings, supported by numerical simulations, indicate that confinement imposes a large mechanical stress on the DNA as evidenced by a pronounced anisotropy and tangent–tangent correlation function with respect to non-constrained DNA. For the strongest confinement we observed nanometer sized hairpins and interwound structures associated with the nicked sites in the DNA sequence. Based on these findings, we propose that spatial DNA confinement in vivo can promote the formation of localized defects at mechanically weak sites that could be co-opted for biological regulatory functions. |
format | Online Article Text |
id | pubmed-5605231 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-56052312017-09-25 Spatial confinement induces hairpins in nicked circular DNA Japaridze, Aleksandre Orlandini, Enzo Smith, Kathleen Beth Gmür, Lucas Valle, Francesco Micheletti, Cristian Dietler, Giovanni Nucleic Acids Res Structural Biology In living cells, DNA is highly confined in space with the help of condensing agents, DNA binding proteins and high levels of supercoiling. Due to challenges associated with experimentally studying DNA under confinement, little is known about the impact of spatial confinement on the local structure of the DNA. Here, we have used well characterized slits of different sizes to collect high resolution atomic force microscopy images of confined circular DNA with the aim of assessing the impact of the spatial confinement on global and local conformational properties of DNA. Our findings, supported by numerical simulations, indicate that confinement imposes a large mechanical stress on the DNA as evidenced by a pronounced anisotropy and tangent–tangent correlation function with respect to non-constrained DNA. For the strongest confinement we observed nanometer sized hairpins and interwound structures associated with the nicked sites in the DNA sequence. Based on these findings, we propose that spatial DNA confinement in vivo can promote the formation of localized defects at mechanically weak sites that could be co-opted for biological regulatory functions. Oxford University Press 2017-05-05 2017-02-15 /pmc/articles/PMC5605231/ /pubmed/28201616 http://dx.doi.org/10.1093/nar/gkx098 Text en © The Author(s) 2017. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Structural Biology Japaridze, Aleksandre Orlandini, Enzo Smith, Kathleen Beth Gmür, Lucas Valle, Francesco Micheletti, Cristian Dietler, Giovanni Spatial confinement induces hairpins in nicked circular DNA |
title | Spatial confinement induces hairpins in nicked circular DNA |
title_full | Spatial confinement induces hairpins in nicked circular DNA |
title_fullStr | Spatial confinement induces hairpins in nicked circular DNA |
title_full_unstemmed | Spatial confinement induces hairpins in nicked circular DNA |
title_short | Spatial confinement induces hairpins in nicked circular DNA |
title_sort | spatial confinement induces hairpins in nicked circular dna |
topic | Structural Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5605231/ https://www.ncbi.nlm.nih.gov/pubmed/28201616 http://dx.doi.org/10.1093/nar/gkx098 |
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