Dynamic remodeling of individual nucleosomes across a eukaryotic genome in response to transcriptional perturbation.

The eukaryotic genome is packaged as chromatin with nucleosomes comprising its basic structural unit, but the detailed structure of chromatin and its dynamic remodeling in terms of individual nucleosome positions has not been completely defined experimentally for any genome. We used ultra-high-throu...

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Autores principales: Sushma Shivaswamy, Akshay Bhinge, Yongjun Zhao, Steven Jones, Martin Hirst, Vishwanath R Iyer
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Lenguaje:EN
Publicado: Public Library of Science (PLoS) 2008
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Acceso en línea:https://doaj.org/article/5cd3341bbfb84f5c85d446cac481a650
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spelling oai:doaj.org-article:5cd3341bbfb84f5c85d446cac481a6502021-11-25T05:33:26ZDynamic remodeling of individual nucleosomes across a eukaryotic genome in response to transcriptional perturbation.1544-91731545-788510.1371/journal.pbio.0060065https://doaj.org/article/5cd3341bbfb84f5c85d446cac481a6502008-03-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/18351804/pdf/?tool=EBIhttps://doaj.org/toc/1544-9173https://doaj.org/toc/1545-7885The eukaryotic genome is packaged as chromatin with nucleosomes comprising its basic structural unit, but the detailed structure of chromatin and its dynamic remodeling in terms of individual nucleosome positions has not been completely defined experimentally for any genome. We used ultra-high-throughput sequencing to map the remodeling of individual nucleosomes throughout the yeast genome before and after a physiological perturbation that causes genome-wide transcriptional changes. Nearly 80% of the genome is covered by positioned nucleosomes occurring in a limited number of stereotypical patterns in relation to transcribed regions and transcription factor binding sites. Chromatin remodeling in response to physiological perturbation was typically associated with the eviction, appearance, or repositioning of one or two nucleosomes in the promoter, rather than broader region-wide changes. Dynamic nucleosome remodeling tends to increase the accessibility of binding sites for transcription factors that mediate transcriptional changes. However, specific nucleosomal rearrangements were also evident at promoters even when there was no apparent transcriptional change, indicating that there is no simple, globally applicable relationship between chromatin remodeling and transcriptional activity. Our study provides a detailed, high-resolution, dynamic map of single-nucleosome remodeling across the yeast genome and its relation to global transcriptional changes.Sushma ShivaswamyAkshay BhingeYongjun ZhaoSteven JonesMartin HirstVishwanath R IyerPublic Library of Science (PLoS)articleBiology (General)QH301-705.5ENPLoS Biology, Vol 6, Iss 3, p e65 (2008)
institution DOAJ
collection DOAJ
language EN
topic Biology (General)
QH301-705.5
spellingShingle Biology (General)
QH301-705.5
Sushma Shivaswamy
Akshay Bhinge
Yongjun Zhao
Steven Jones
Martin Hirst
Vishwanath R Iyer
Dynamic remodeling of individual nucleosomes across a eukaryotic genome in response to transcriptional perturbation.
description The eukaryotic genome is packaged as chromatin with nucleosomes comprising its basic structural unit, but the detailed structure of chromatin and its dynamic remodeling in terms of individual nucleosome positions has not been completely defined experimentally for any genome. We used ultra-high-throughput sequencing to map the remodeling of individual nucleosomes throughout the yeast genome before and after a physiological perturbation that causes genome-wide transcriptional changes. Nearly 80% of the genome is covered by positioned nucleosomes occurring in a limited number of stereotypical patterns in relation to transcribed regions and transcription factor binding sites. Chromatin remodeling in response to physiological perturbation was typically associated with the eviction, appearance, or repositioning of one or two nucleosomes in the promoter, rather than broader region-wide changes. Dynamic nucleosome remodeling tends to increase the accessibility of binding sites for transcription factors that mediate transcriptional changes. However, specific nucleosomal rearrangements were also evident at promoters even when there was no apparent transcriptional change, indicating that there is no simple, globally applicable relationship between chromatin remodeling and transcriptional activity. Our study provides a detailed, high-resolution, dynamic map of single-nucleosome remodeling across the yeast genome and its relation to global transcriptional changes.
format article
author Sushma Shivaswamy
Akshay Bhinge
Yongjun Zhao
Steven Jones
Martin Hirst
Vishwanath R Iyer
author_facet Sushma Shivaswamy
Akshay Bhinge
Yongjun Zhao
Steven Jones
Martin Hirst
Vishwanath R Iyer
author_sort Sushma Shivaswamy
title Dynamic remodeling of individual nucleosomes across a eukaryotic genome in response to transcriptional perturbation.
title_short Dynamic remodeling of individual nucleosomes across a eukaryotic genome in response to transcriptional perturbation.
title_full Dynamic remodeling of individual nucleosomes across a eukaryotic genome in response to transcriptional perturbation.
title_fullStr Dynamic remodeling of individual nucleosomes across a eukaryotic genome in response to transcriptional perturbation.
title_full_unstemmed Dynamic remodeling of individual nucleosomes across a eukaryotic genome in response to transcriptional perturbation.
title_sort dynamic remodeling of individual nucleosomes across a eukaryotic genome in response to transcriptional perturbation.
publisher Public Library of Science (PLoS)
publishDate 2008
url https://doaj.org/article/5cd3341bbfb84f5c85d446cac481a650
work_keys_str_mv AT sushmashivaswamy dynamicremodelingofindividualnucleosomesacrossaeukaryoticgenomeinresponsetotranscriptionalperturbation
AT akshaybhinge dynamicremodelingofindividualnucleosomesacrossaeukaryoticgenomeinresponsetotranscriptionalperturbation
AT yongjunzhao dynamicremodelingofindividualnucleosomesacrossaeukaryoticgenomeinresponsetotranscriptionalperturbation
AT stevenjones dynamicremodelingofindividualnucleosomesacrossaeukaryoticgenomeinresponsetotranscriptionalperturbation
AT martinhirst dynamicremodelingofindividualnucleosomesacrossaeukaryoticgenomeinresponsetotranscriptionalperturbation
AT vishwanathriyer dynamicremodelingofindividualnucleosomesacrossaeukaryoticgenomeinresponsetotranscriptionalperturbation
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