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Strand-specific RNA sequencing reveals extensive regulated long antisense transcripts that are conserved across yeast species
BACKGROUND: Recent studies in budding yeast have shown that antisense transcription occurs at many loci. However, the functional role of antisense transcripts has been demonstrated only in a few cases and it has been suggested that most antisense transcripts may result from promiscuous bi-directiona...
Autores principales: | , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2945789/ https://www.ncbi.nlm.nih.gov/pubmed/20796282 http://dx.doi.org/10.1186/gb-2010-11-8-r87 |
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author | Yassour, Moran Pfiffner, Jenna Levin, Joshua Z Adiconis, Xian Gnirke, Andreas Nusbaum, Chad Thompson, Dawn-Anne Friedman, Nir Regev, Aviv |
author_facet | Yassour, Moran Pfiffner, Jenna Levin, Joshua Z Adiconis, Xian Gnirke, Andreas Nusbaum, Chad Thompson, Dawn-Anne Friedman, Nir Regev, Aviv |
author_sort | Yassour, Moran |
collection | PubMed |
description | BACKGROUND: Recent studies in budding yeast have shown that antisense transcription occurs at many loci. However, the functional role of antisense transcripts has been demonstrated only in a few cases and it has been suggested that most antisense transcripts may result from promiscuous bi-directional transcription in a dense genome. RESULTS: Here, we use strand-specific RNA sequencing to study anti-sense transcription in Saccharomyces cerevisiae. We detect 1,103 putative antisense transcripts expressed in mid-log phase growth, ranging from 39 short transcripts covering only the 3' UTR of sense genes to 145 long transcripts covering the entire sense open reading frame. Many of these antisense transcripts overlap sense genes that are repressed in mid-log phase and are important in stationary phase, stress response, or meiosis. We validate the differential regulation of 67 antisense transcripts and their sense targets in relevant conditions, including nutrient limitation and environmental stresses. Moreover, we show that several antisense transcripts and, in some cases, their differential expression have been conserved across five species of yeast spanning 150 million years of evolution. Divergence in the regulation of antisense transcripts to two respiratory genes coincides with the evolution of respiro-fermentation. CONCLUSIONS: Our work provides support for a global and conserved role for antisense transcription in yeast gene regulation. |
format | Text |
id | pubmed-2945789 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-29457892010-09-28 Strand-specific RNA sequencing reveals extensive regulated long antisense transcripts that are conserved across yeast species Yassour, Moran Pfiffner, Jenna Levin, Joshua Z Adiconis, Xian Gnirke, Andreas Nusbaum, Chad Thompson, Dawn-Anne Friedman, Nir Regev, Aviv Genome Biol Research BACKGROUND: Recent studies in budding yeast have shown that antisense transcription occurs at many loci. However, the functional role of antisense transcripts has been demonstrated only in a few cases and it has been suggested that most antisense transcripts may result from promiscuous bi-directional transcription in a dense genome. RESULTS: Here, we use strand-specific RNA sequencing to study anti-sense transcription in Saccharomyces cerevisiae. We detect 1,103 putative antisense transcripts expressed in mid-log phase growth, ranging from 39 short transcripts covering only the 3' UTR of sense genes to 145 long transcripts covering the entire sense open reading frame. Many of these antisense transcripts overlap sense genes that are repressed in mid-log phase and are important in stationary phase, stress response, or meiosis. We validate the differential regulation of 67 antisense transcripts and their sense targets in relevant conditions, including nutrient limitation and environmental stresses. Moreover, we show that several antisense transcripts and, in some cases, their differential expression have been conserved across five species of yeast spanning 150 million years of evolution. Divergence in the regulation of antisense transcripts to two respiratory genes coincides with the evolution of respiro-fermentation. CONCLUSIONS: Our work provides support for a global and conserved role for antisense transcription in yeast gene regulation. BioMed Central 2010 2010-08-26 /pmc/articles/PMC2945789/ /pubmed/20796282 http://dx.doi.org/10.1186/gb-2010-11-8-r87 Text en Copyright ©2010 Yassour et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Yassour, Moran Pfiffner, Jenna Levin, Joshua Z Adiconis, Xian Gnirke, Andreas Nusbaum, Chad Thompson, Dawn-Anne Friedman, Nir Regev, Aviv Strand-specific RNA sequencing reveals extensive regulated long antisense transcripts that are conserved across yeast species |
title | Strand-specific RNA sequencing reveals extensive regulated long antisense transcripts that are conserved across yeast species |
title_full | Strand-specific RNA sequencing reveals extensive regulated long antisense transcripts that are conserved across yeast species |
title_fullStr | Strand-specific RNA sequencing reveals extensive regulated long antisense transcripts that are conserved across yeast species |
title_full_unstemmed | Strand-specific RNA sequencing reveals extensive regulated long antisense transcripts that are conserved across yeast species |
title_short | Strand-specific RNA sequencing reveals extensive regulated long antisense transcripts that are conserved across yeast species |
title_sort | strand-specific rna sequencing reveals extensive regulated long antisense transcripts that are conserved across yeast species |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2945789/ https://www.ncbi.nlm.nih.gov/pubmed/20796282 http://dx.doi.org/10.1186/gb-2010-11-8-r87 |
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