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The implication of DNA bending energy for nucleosome positioning and sliding

Nucleosome not only directly affects cellular processes, such as DNA replication, recombination, and transcription, but also severs as a fundamentally important target of epigenetic modifications. Our previous study indicated that the bending property of DNA is important in nucleosome formation, par...

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Autores principales: Liu, Guoqing, Xing, Yongqiang, Zhao, Hongyu, Cai, Lu, Wang, Jianying
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5995830/
https://www.ncbi.nlm.nih.gov/pubmed/29891930
http://dx.doi.org/10.1038/s41598-018-27247-x
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author Liu, Guoqing
Xing, Yongqiang
Zhao, Hongyu
Cai, Lu
Wang, Jianying
author_facet Liu, Guoqing
Xing, Yongqiang
Zhao, Hongyu
Cai, Lu
Wang, Jianying
author_sort Liu, Guoqing
collection PubMed
description Nucleosome not only directly affects cellular processes, such as DNA replication, recombination, and transcription, but also severs as a fundamentally important target of epigenetic modifications. Our previous study indicated that the bending property of DNA is important in nucleosome formation, particularly in predicting the dyad positions of nucleosomes on a DNA segment. Here, we investigated the role of bending energy in nucleosome positioning and sliding in depth to decipher sequence-directed mechanism. The results show that bending energy is a good physical index to predict the free energy in the process of nucleosome reconstitution in vitro. Our data also imply that there are at least 20% of the nucleosomes in budding yeast do not adopt canonical positioning, in which underlying sequences wrapped around histones are structurally symmetric. We also revealed distinct patterns of bending energy profile for distinctly organized chromatin structures, such as well-positioned nucleosomes, fuzzy nucleosomes, and linker regions and discussed nucleosome sliding in terms of bending energy. We proposed that the stability of a nucleosome is positively correlated with the strength of the bending anisotropy of DNA segment, and both accessibility and directionality of nucleosome sliding is likely to be modulated by diverse patterns of DNA bending energy profile.
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spelling pubmed-59958302018-06-21 The implication of DNA bending energy for nucleosome positioning and sliding Liu, Guoqing Xing, Yongqiang Zhao, Hongyu Cai, Lu Wang, Jianying Sci Rep Article Nucleosome not only directly affects cellular processes, such as DNA replication, recombination, and transcription, but also severs as a fundamentally important target of epigenetic modifications. Our previous study indicated that the bending property of DNA is important in nucleosome formation, particularly in predicting the dyad positions of nucleosomes on a DNA segment. Here, we investigated the role of bending energy in nucleosome positioning and sliding in depth to decipher sequence-directed mechanism. The results show that bending energy is a good physical index to predict the free energy in the process of nucleosome reconstitution in vitro. Our data also imply that there are at least 20% of the nucleosomes in budding yeast do not adopt canonical positioning, in which underlying sequences wrapped around histones are structurally symmetric. We also revealed distinct patterns of bending energy profile for distinctly organized chromatin structures, such as well-positioned nucleosomes, fuzzy nucleosomes, and linker regions and discussed nucleosome sliding in terms of bending energy. We proposed that the stability of a nucleosome is positively correlated with the strength of the bending anisotropy of DNA segment, and both accessibility and directionality of nucleosome sliding is likely to be modulated by diverse patterns of DNA bending energy profile. Nature Publishing Group UK 2018-06-11 /pmc/articles/PMC5995830/ /pubmed/29891930 http://dx.doi.org/10.1038/s41598-018-27247-x Text en © The Author(s) 2018 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
Liu, Guoqing
Xing, Yongqiang
Zhao, Hongyu
Cai, Lu
Wang, Jianying
The implication of DNA bending energy for nucleosome positioning and sliding
title The implication of DNA bending energy for nucleosome positioning and sliding
title_full The implication of DNA bending energy for nucleosome positioning and sliding
title_fullStr The implication of DNA bending energy for nucleosome positioning and sliding
title_full_unstemmed The implication of DNA bending energy for nucleosome positioning and sliding
title_short The implication of DNA bending energy for nucleosome positioning and sliding
title_sort implication of dna bending energy for nucleosome positioning and sliding
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5995830/
https://www.ncbi.nlm.nih.gov/pubmed/29891930
http://dx.doi.org/10.1038/s41598-018-27247-x
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