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Divergence of a conserved elongation factor and transcription regulation in budding and fission yeast
Complex regulation of gene expression in mammals has evolved from simpler eukaryotic systems, yet the mechanistic features of this evolution remain elusive. Here, we compared the transcriptional landscapes of the distantly related budding and fission yeast. We adapted the Precision Run-On sequencing...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory Press
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4889974/ https://www.ncbi.nlm.nih.gov/pubmed/27197211 http://dx.doi.org/10.1101/gr.204578.116 |
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author | Booth, Gregory T. Wang, Isabel X. Cheung, Vivian G. Lis, John T. |
author_facet | Booth, Gregory T. Wang, Isabel X. Cheung, Vivian G. Lis, John T. |
author_sort | Booth, Gregory T. |
collection | PubMed |
description | Complex regulation of gene expression in mammals has evolved from simpler eukaryotic systems, yet the mechanistic features of this evolution remain elusive. Here, we compared the transcriptional landscapes of the distantly related budding and fission yeast. We adapted the Precision Run-On sequencing (PRO-seq) approach to map the positions of RNA polymerase active sites genome-wide in Schizosaccharomyces pombe and Saccharomyces cerevisiae. Additionally, we mapped preferred sites of transcription initiation in each organism using PRO-cap. Unexpectedly, we identify a pause in early elongation, specific to S. pombe, that requires the conserved elongation factor subunit Spt4 and resembles promoter-proximal pausing in metazoans. PRO-seq profiles in strains lacking Spt4 reveal globally elevated levels of transcribing RNA Polymerase II (Pol II) within genes in both species. Messenger RNA abundance, however, does not reflect the increases in Pol II density, indicating a global reduction in elongation rate. Together, our results provide the first base-pair resolution map of transcription elongation in S. pombe and identify divergent roles for Spt4 in controlling elongation in budding and fission yeast. |
format | Online Article Text |
id | pubmed-4889974 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Cold Spring Harbor Laboratory Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-48899742016-12-01 Divergence of a conserved elongation factor and transcription regulation in budding and fission yeast Booth, Gregory T. Wang, Isabel X. Cheung, Vivian G. Lis, John T. Genome Res Research Complex regulation of gene expression in mammals has evolved from simpler eukaryotic systems, yet the mechanistic features of this evolution remain elusive. Here, we compared the transcriptional landscapes of the distantly related budding and fission yeast. We adapted the Precision Run-On sequencing (PRO-seq) approach to map the positions of RNA polymerase active sites genome-wide in Schizosaccharomyces pombe and Saccharomyces cerevisiae. Additionally, we mapped preferred sites of transcription initiation in each organism using PRO-cap. Unexpectedly, we identify a pause in early elongation, specific to S. pombe, that requires the conserved elongation factor subunit Spt4 and resembles promoter-proximal pausing in metazoans. PRO-seq profiles in strains lacking Spt4 reveal globally elevated levels of transcribing RNA Polymerase II (Pol II) within genes in both species. Messenger RNA abundance, however, does not reflect the increases in Pol II density, indicating a global reduction in elongation rate. Together, our results provide the first base-pair resolution map of transcription elongation in S. pombe and identify divergent roles for Spt4 in controlling elongation in budding and fission yeast. Cold Spring Harbor Laboratory Press 2016-06 /pmc/articles/PMC4889974/ /pubmed/27197211 http://dx.doi.org/10.1101/gr.204578.116 Text en © 2016 Booth et al.; Published by Cold Spring Harbor Laboratory Press http://creativecommons.org/licenses/by-nc/4.0/ This article is distributed exclusively by Cold Spring Harbor Laboratory Press for the first six months after the full-issue publication date (see http://genome.cshlp.org/site/misc/terms.xhtml). After six months, it is available under a Creative Commons License (Attribution-NonCommercial 4.0 International), as described at http://creativecommons.org/licenses/by-nc/4.0/. |
spellingShingle | Research Booth, Gregory T. Wang, Isabel X. Cheung, Vivian G. Lis, John T. Divergence of a conserved elongation factor and transcription regulation in budding and fission yeast |
title | Divergence of a conserved elongation factor and transcription regulation in budding and fission yeast |
title_full | Divergence of a conserved elongation factor and transcription regulation in budding and fission yeast |
title_fullStr | Divergence of a conserved elongation factor and transcription regulation in budding and fission yeast |
title_full_unstemmed | Divergence of a conserved elongation factor and transcription regulation in budding and fission yeast |
title_short | Divergence of a conserved elongation factor and transcription regulation in budding and fission yeast |
title_sort | divergence of a conserved elongation factor and transcription regulation in budding and fission yeast |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4889974/ https://www.ncbi.nlm.nih.gov/pubmed/27197211 http://dx.doi.org/10.1101/gr.204578.116 |
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