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Categorical spectral analysis of periodicity in nucleosomal DNA
DNA helical twist imposes geometric constraints on the location of histone–DNA interaction sites along nucleosomal DNA. Certain 10.5-bp periodic nucleotides in phase with these geometric constraints have been suggested to facilitate nucleosome positioning. However, the extent of nucleotide periodici...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4797311/ https://www.ncbi.nlm.nih.gov/pubmed/26893354 http://dx.doi.org/10.1093/nar/gkw101 |
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author | Jin, Hu Rube, H. Tomas Song, Jun S. |
author_facet | Jin, Hu Rube, H. Tomas Song, Jun S. |
author_sort | Jin, Hu |
collection | PubMed |
description | DNA helical twist imposes geometric constraints on the location of histone–DNA interaction sites along nucleosomal DNA. Certain 10.5-bp periodic nucleotides in phase with these geometric constraints have been suggested to facilitate nucleosome positioning. However, the extent of nucleotide periodicity in nucleosomal DNA and its significance in directing nucleosome positioning still remain unclear. We clarify these issues by applying categorical spectral analysis to high-resolution nucleosome maps in two yeast species. We find that only a small fraction of nucleosomal sequences contain significant 10.5-bp periodicity. We further develop a spectral decomposition method to show that the previously observed periodicity in aligned nucleosomal sequences mainly results from proper phasing among nucleosomal sequences, and not from a preponderant occurrence of periodicity within individual sequences. Importantly, we show that this phasing may arise from the histones’ proclivity for putting preferred nucleotides at some of the evenly spaced histone–DNA contact points with respect to the dyad axis. We demonstrate that 10.5-bp periodicity, when present, significantly facilitates rotational, but not translational, nucleosome positioning. Finally, although periodicity only moderately affects nucleosome occupancy genome wide, reduced periodicity is an evolutionarily conserved signature of nucleosome-depleted regions around transcription start/termination sites. |
format | Online Article Text |
id | pubmed-4797311 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-47973112016-03-21 Categorical spectral analysis of periodicity in nucleosomal DNA Jin, Hu Rube, H. Tomas Song, Jun S. Nucleic Acids Res Computational Biology DNA helical twist imposes geometric constraints on the location of histone–DNA interaction sites along nucleosomal DNA. Certain 10.5-bp periodic nucleotides in phase with these geometric constraints have been suggested to facilitate nucleosome positioning. However, the extent of nucleotide periodicity in nucleosomal DNA and its significance in directing nucleosome positioning still remain unclear. We clarify these issues by applying categorical spectral analysis to high-resolution nucleosome maps in two yeast species. We find that only a small fraction of nucleosomal sequences contain significant 10.5-bp periodicity. We further develop a spectral decomposition method to show that the previously observed periodicity in aligned nucleosomal sequences mainly results from proper phasing among nucleosomal sequences, and not from a preponderant occurrence of periodicity within individual sequences. Importantly, we show that this phasing may arise from the histones’ proclivity for putting preferred nucleotides at some of the evenly spaced histone–DNA contact points with respect to the dyad axis. We demonstrate that 10.5-bp periodicity, when present, significantly facilitates rotational, but not translational, nucleosome positioning. Finally, although periodicity only moderately affects nucleosome occupancy genome wide, reduced periodicity is an evolutionarily conserved signature of nucleosome-depleted regions around transcription start/termination sites. Oxford University Press 2016-03-18 2016-02-17 /pmc/articles/PMC4797311/ /pubmed/26893354 http://dx.doi.org/10.1093/nar/gkw101 Text en © The Author(s) 2016. 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 | Computational Biology Jin, Hu Rube, H. Tomas Song, Jun S. Categorical spectral analysis of periodicity in nucleosomal DNA |
title | Categorical spectral analysis of periodicity in nucleosomal DNA |
title_full | Categorical spectral analysis of periodicity in nucleosomal DNA |
title_fullStr | Categorical spectral analysis of periodicity in nucleosomal DNA |
title_full_unstemmed | Categorical spectral analysis of periodicity in nucleosomal DNA |
title_short | Categorical spectral analysis of periodicity in nucleosomal DNA |
title_sort | categorical spectral analysis of periodicity in nucleosomal dna |
topic | Computational Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4797311/ https://www.ncbi.nlm.nih.gov/pubmed/26893354 http://dx.doi.org/10.1093/nar/gkw101 |
work_keys_str_mv | AT jinhu categoricalspectralanalysisofperiodicityinnucleosomaldna AT rubehtomas categoricalspectralanalysisofperiodicityinnucleosomaldna AT songjuns categoricalspectralanalysisofperiodicityinnucleosomaldna |