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Nucleosome positioning sequence patterns as packing or regulatory

Nucleosome positioning DNA sequence patterns (NPS)—usually distributions of particular dinucleotides or other sequence elements in nucleosomal DNA—at least partially determine chromatin structure and arrangements of nucleosomes that in turn affect gene expression. Statistically, NPS are defined as o...

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Autores principales: Pranckeviciene, Erinija, Hosid, Sergey, Liang, Nathan, Ioshikhes, Ilya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7004410/
https://www.ncbi.nlm.nih.gov/pubmed/31986131
http://dx.doi.org/10.1371/journal.pcbi.1007365
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author Pranckeviciene, Erinija
Hosid, Sergey
Liang, Nathan
Ioshikhes, Ilya
author_facet Pranckeviciene, Erinija
Hosid, Sergey
Liang, Nathan
Ioshikhes, Ilya
author_sort Pranckeviciene, Erinija
collection PubMed
description Nucleosome positioning DNA sequence patterns (NPS)—usually distributions of particular dinucleotides or other sequence elements in nucleosomal DNA—at least partially determine chromatin structure and arrangements of nucleosomes that in turn affect gene expression. Statistically, NPS are defined as oscillations of the dinucleotide periodicity of about 10 base pairs (bp) which reflects the double helix period. We compared the nucleosomal DNA patterns in mouse, human and yeast organisms and observed few distinctive patterns that can be termed as packing and regulatory referring to distinctive modes of chromatin function. For the first time the NPS patterns in nucleus accumbens cells (NAC) in mouse brain were characterized and compared to the patterns in human CD4+ and apoptotic lymphocyte cells and well studied patterns in yeast. The NPS patterns in human CD4+ cells and mouse brain cells had very high positive correlation. However, there was no correlation between them and patterns in human apoptotic lymphocyte cells and yeast, but the latter two were highly correlated with each other. By their dinucleotide arrangements the analyzed NPS patterns classified into stable canonical WW/SS (W = A or T and S = C or G dinucleotide) and less stable RR/YY (R = A or G and Y = C or T dinucleotide) patterns and anti-patterns. In the anti-patterns positioning of the dinucleotides is flipped compared to those in the regular patterns. Stable canonical WW/SS patterns and anti-patterns are ubiquitously observed in many organisms and they had high resemblance between yeast and human apoptotic cells. Less stable RR/YY patterns had higher positive correlation between mouse and normal human cells. Our analysis and evidence from scientific literature lead to idea that various distinct patterns in nucleosomal DNA can be related to the two roles of the chromatin: packing (WW/SS) and regulatory (RR/YY and “anti”).
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spelling pubmed-70044102020-02-19 Nucleosome positioning sequence patterns as packing or regulatory Pranckeviciene, Erinija Hosid, Sergey Liang, Nathan Ioshikhes, Ilya PLoS Comput Biol Research Article Nucleosome positioning DNA sequence patterns (NPS)—usually distributions of particular dinucleotides or other sequence elements in nucleosomal DNA—at least partially determine chromatin structure and arrangements of nucleosomes that in turn affect gene expression. Statistically, NPS are defined as oscillations of the dinucleotide periodicity of about 10 base pairs (bp) which reflects the double helix period. We compared the nucleosomal DNA patterns in mouse, human and yeast organisms and observed few distinctive patterns that can be termed as packing and regulatory referring to distinctive modes of chromatin function. For the first time the NPS patterns in nucleus accumbens cells (NAC) in mouse brain were characterized and compared to the patterns in human CD4+ and apoptotic lymphocyte cells and well studied patterns in yeast. The NPS patterns in human CD4+ cells and mouse brain cells had very high positive correlation. However, there was no correlation between them and patterns in human apoptotic lymphocyte cells and yeast, but the latter two were highly correlated with each other. By their dinucleotide arrangements the analyzed NPS patterns classified into stable canonical WW/SS (W = A or T and S = C or G dinucleotide) and less stable RR/YY (R = A or G and Y = C or T dinucleotide) patterns and anti-patterns. In the anti-patterns positioning of the dinucleotides is flipped compared to those in the regular patterns. Stable canonical WW/SS patterns and anti-patterns are ubiquitously observed in many organisms and they had high resemblance between yeast and human apoptotic cells. Less stable RR/YY patterns had higher positive correlation between mouse and normal human cells. Our analysis and evidence from scientific literature lead to idea that various distinct patterns in nucleosomal DNA can be related to the two roles of the chromatin: packing (WW/SS) and regulatory (RR/YY and “anti”). Public Library of Science 2020-01-27 /pmc/articles/PMC7004410/ /pubmed/31986131 http://dx.doi.org/10.1371/journal.pcbi.1007365 Text en © 2020 Pranckeviciene et al 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 use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Pranckeviciene, Erinija
Hosid, Sergey
Liang, Nathan
Ioshikhes, Ilya
Nucleosome positioning sequence patterns as packing or regulatory
title Nucleosome positioning sequence patterns as packing or regulatory
title_full Nucleosome positioning sequence patterns as packing or regulatory
title_fullStr Nucleosome positioning sequence patterns as packing or regulatory
title_full_unstemmed Nucleosome positioning sequence patterns as packing or regulatory
title_short Nucleosome positioning sequence patterns as packing or regulatory
title_sort nucleosome positioning sequence patterns as packing or regulatory
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7004410/
https://www.ncbi.nlm.nih.gov/pubmed/31986131
http://dx.doi.org/10.1371/journal.pcbi.1007365
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