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DNA accessibility of chromatosomes quantified by automated image analysis of AFM data

DNA compaction and accessibility in eukaryotes are governed by nucleosomes and orchestrated through interactions between DNA and DNA-binding proteins. Using QuantAFM, a method for automated image analysis of atomic force microscopy (AFM) data, we performed a detailed statistical analysis of structur...

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Autores principales: Würtz, Martin, Aumiller, Dennis, Gundelwein, Lina, Jung, Philipp, Schütz, Christian, Lehmann, Kathrin, Tóth, Katalin, Rohr, Karl
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6726762/
https://www.ncbi.nlm.nih.gov/pubmed/31484969
http://dx.doi.org/10.1038/s41598-019-49163-4
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author Würtz, Martin
Aumiller, Dennis
Gundelwein, Lina
Jung, Philipp
Schütz, Christian
Lehmann, Kathrin
Tóth, Katalin
Rohr, Karl
author_facet Würtz, Martin
Aumiller, Dennis
Gundelwein, Lina
Jung, Philipp
Schütz, Christian
Lehmann, Kathrin
Tóth, Katalin
Rohr, Karl
author_sort Würtz, Martin
collection PubMed
description DNA compaction and accessibility in eukaryotes are governed by nucleosomes and orchestrated through interactions between DNA and DNA-binding proteins. Using QuantAFM, a method for automated image analysis of atomic force microscopy (AFM) data, we performed a detailed statistical analysis of structural properties of mono-nucleosomes. QuantAFM allows fast analysis of AFM images, including image preprocessing, object segmentation, and quantification of different structural parameters to assess DNA accessibility of nucleosomes. A comparison of nucleosomes reconstituted with and without linker histone H1 quantified H1’s already described ability of compacting the nucleosome. We further employed nucleosomes bearing two charge-modifying mutations at position R81 and R88 in histone H2A (H2A R81E/R88E) to characterize DNA accessibility under destabilizing conditions. Upon H2A mutation, even in presence of H1, the DNA opening angle at the entry/exit site was increased and the DNA wrapping length around the histone core was reduced. Interestingly, a distinct opening of the less bendable DNA side was observed upon H2A mutation, indicating an enhancement of the intrinsic asymmetry of the Widom-601 nucleosomes. This study validates AFM as a technique to investigate structural parameters of nucleosomes and highlights how the DNA sequence, together with nucleosome modifications, can influence the DNA accessibility.
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spelling pubmed-67267622019-09-18 DNA accessibility of chromatosomes quantified by automated image analysis of AFM data Würtz, Martin Aumiller, Dennis Gundelwein, Lina Jung, Philipp Schütz, Christian Lehmann, Kathrin Tóth, Katalin Rohr, Karl Sci Rep Article DNA compaction and accessibility in eukaryotes are governed by nucleosomes and orchestrated through interactions between DNA and DNA-binding proteins. Using QuantAFM, a method for automated image analysis of atomic force microscopy (AFM) data, we performed a detailed statistical analysis of structural properties of mono-nucleosomes. QuantAFM allows fast analysis of AFM images, including image preprocessing, object segmentation, and quantification of different structural parameters to assess DNA accessibility of nucleosomes. A comparison of nucleosomes reconstituted with and without linker histone H1 quantified H1’s already described ability of compacting the nucleosome. We further employed nucleosomes bearing two charge-modifying mutations at position R81 and R88 in histone H2A (H2A R81E/R88E) to characterize DNA accessibility under destabilizing conditions. Upon H2A mutation, even in presence of H1, the DNA opening angle at the entry/exit site was increased and the DNA wrapping length around the histone core was reduced. Interestingly, a distinct opening of the less bendable DNA side was observed upon H2A mutation, indicating an enhancement of the intrinsic asymmetry of the Widom-601 nucleosomes. This study validates AFM as a technique to investigate structural parameters of nucleosomes and highlights how the DNA sequence, together with nucleosome modifications, can influence the DNA accessibility. Nature Publishing Group UK 2019-09-04 /pmc/articles/PMC6726762/ /pubmed/31484969 http://dx.doi.org/10.1038/s41598-019-49163-4 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Würtz, Martin
Aumiller, Dennis
Gundelwein, Lina
Jung, Philipp
Schütz, Christian
Lehmann, Kathrin
Tóth, Katalin
Rohr, Karl
DNA accessibility of chromatosomes quantified by automated image analysis of AFM data
title DNA accessibility of chromatosomes quantified by automated image analysis of AFM data
title_full DNA accessibility of chromatosomes quantified by automated image analysis of AFM data
title_fullStr DNA accessibility of chromatosomes quantified by automated image analysis of AFM data
title_full_unstemmed DNA accessibility of chromatosomes quantified by automated image analysis of AFM data
title_short DNA accessibility of chromatosomes quantified by automated image analysis of AFM data
title_sort dna accessibility of chromatosomes quantified by automated image analysis of afm data
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6726762/
https://www.ncbi.nlm.nih.gov/pubmed/31484969
http://dx.doi.org/10.1038/s41598-019-49163-4
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