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Comprehensive analysis of promoter-proximal RNA polymerase II pausing across mammalian cell types

BACKGROUND: For many genes, RNA polymerase II stably pauses before transitioning to productive elongation. Although polymerase II pausing has been shown to be a mechanism for regulating transcriptional activation, the extent to which it is involved in control of mammalian gene expression and its rel...

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Autores principales: Day, Daniel S., Zhang, Bing, Stevens, Sean M., Ferrari, Francesco, Larschan, Erica N., Park, Peter J., Pu, William T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4893286/
https://www.ncbi.nlm.nih.gov/pubmed/27259512
http://dx.doi.org/10.1186/s13059-016-0984-2
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author Day, Daniel S.
Zhang, Bing
Stevens, Sean M.
Ferrari, Francesco
Larschan, Erica N.
Park, Peter J.
Pu, William T.
author_facet Day, Daniel S.
Zhang, Bing
Stevens, Sean M.
Ferrari, Francesco
Larschan, Erica N.
Park, Peter J.
Pu, William T.
author_sort Day, Daniel S.
collection PubMed
description BACKGROUND: For many genes, RNA polymerase II stably pauses before transitioning to productive elongation. Although polymerase II pausing has been shown to be a mechanism for regulating transcriptional activation, the extent to which it is involved in control of mammalian gene expression and its relationship to chromatin structure remain poorly understood. RESULTS: Here, we analyze 85 RNA polymerase II chromatin immunoprecipitation (ChIP)-sequencing experiments from 35 different murine and human samples, as well as related genome-wide datasets, to gain new insights into the relationship between polymerase II pausing and gene regulation. Across cell and tissue types, paused genes (pausing index > 2) comprise approximately 60 % of expressed genes and are repeatedly associated with specific biological functions. Paused genes also have lower cell-to-cell expression variability. Increased pausing has a non-linear effect on gene expression levels, with moderately paused genes being expressed more highly than other paused genes. The highest gene expression levels are often achieved through a novel pause-release mechanism driven by high polymerase II initiation. In three datasets examining the impact of extracellular signals, genes responsive to stimulus have slightly lower pausing index on average than non-responsive genes, and rapid gene activation is linked to conditional pause-release. Both chromatin structure and local sequence composition near the transcription start site influence pausing, with divergent features between mammals and Drosophila. Most notably, in mammals pausing is positively correlated with histone H2A.Z occupancy at promoters. CONCLUSIONS: Our results provide new insights into the contribution of RNA polymerase II pausing in mammalian gene regulation and chromatin structure. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13059-016-0984-2) contains supplementary material, which is available to authorized users.
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spelling pubmed-48932862016-06-05 Comprehensive analysis of promoter-proximal RNA polymerase II pausing across mammalian cell types Day, Daniel S. Zhang, Bing Stevens, Sean M. Ferrari, Francesco Larschan, Erica N. Park, Peter J. Pu, William T. Genome Biol Research BACKGROUND: For many genes, RNA polymerase II stably pauses before transitioning to productive elongation. Although polymerase II pausing has been shown to be a mechanism for regulating transcriptional activation, the extent to which it is involved in control of mammalian gene expression and its relationship to chromatin structure remain poorly understood. RESULTS: Here, we analyze 85 RNA polymerase II chromatin immunoprecipitation (ChIP)-sequencing experiments from 35 different murine and human samples, as well as related genome-wide datasets, to gain new insights into the relationship between polymerase II pausing and gene regulation. Across cell and tissue types, paused genes (pausing index > 2) comprise approximately 60 % of expressed genes and are repeatedly associated with specific biological functions. Paused genes also have lower cell-to-cell expression variability. Increased pausing has a non-linear effect on gene expression levels, with moderately paused genes being expressed more highly than other paused genes. The highest gene expression levels are often achieved through a novel pause-release mechanism driven by high polymerase II initiation. In three datasets examining the impact of extracellular signals, genes responsive to stimulus have slightly lower pausing index on average than non-responsive genes, and rapid gene activation is linked to conditional pause-release. Both chromatin structure and local sequence composition near the transcription start site influence pausing, with divergent features between mammals and Drosophila. Most notably, in mammals pausing is positively correlated with histone H2A.Z occupancy at promoters. CONCLUSIONS: Our results provide new insights into the contribution of RNA polymerase II pausing in mammalian gene regulation and chromatin structure. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13059-016-0984-2) contains supplementary material, which is available to authorized users. BioMed Central 2016-06-03 /pmc/articles/PMC4893286/ /pubmed/27259512 http://dx.doi.org/10.1186/s13059-016-0984-2 Text en © The Author(s). 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Day, Daniel S.
Zhang, Bing
Stevens, Sean M.
Ferrari, Francesco
Larschan, Erica N.
Park, Peter J.
Pu, William T.
Comprehensive analysis of promoter-proximal RNA polymerase II pausing across mammalian cell types
title Comprehensive analysis of promoter-proximal RNA polymerase II pausing across mammalian cell types
title_full Comprehensive analysis of promoter-proximal RNA polymerase II pausing across mammalian cell types
title_fullStr Comprehensive analysis of promoter-proximal RNA polymerase II pausing across mammalian cell types
title_full_unstemmed Comprehensive analysis of promoter-proximal RNA polymerase II pausing across mammalian cell types
title_short Comprehensive analysis of promoter-proximal RNA polymerase II pausing across mammalian cell types
title_sort comprehensive analysis of promoter-proximal rna polymerase ii pausing across mammalian cell types
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4893286/
https://www.ncbi.nlm.nih.gov/pubmed/27259512
http://dx.doi.org/10.1186/s13059-016-0984-2
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