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Contributions of transcription and mRNA decay to gene expression dynamics of fission yeast in response to oxidative stress
The cooperation of transcriptional and post-transcriptional levels of control to shape gene regulation is only partially understood. Here we show that a combination of two simple and non-invasive genomic techniques, coupled with kinetic mathematical modeling, affords insight into the intricate dynam...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Landes Bioscience
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4156502/ https://www.ncbi.nlm.nih.gov/pubmed/25007214 http://dx.doi.org/10.4161/rna.29196 |
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author | Marguerat, Samuel Lawler, Katherine Brazma, Alvis Bähler, Jürg |
author_facet | Marguerat, Samuel Lawler, Katherine Brazma, Alvis Bähler, Jürg |
author_sort | Marguerat, Samuel |
collection | PubMed |
description | The cooperation of transcriptional and post-transcriptional levels of control to shape gene regulation is only partially understood. Here we show that a combination of two simple and non-invasive genomic techniques, coupled with kinetic mathematical modeling, affords insight into the intricate dynamics of RNA regulation in response to oxidative stress in the fission yeast Schizosaccharomyces pombe. This study reveals a dominant role of transcriptional regulation in response to stress, but also points to the first minutes after stress induction as a critical time when the coordinated control of mRNA turnover can support the control of transcription for rapid gene regulation. In addition, we uncover specialized gene expression strategies associated with distinct functional gene groups, such as simultaneous transcriptional repression and mRNA destabilization for genes encoding ribosomal proteins, delayed mRNA destabilization with varying contribution of transcription for ribosome biogenesis genes, dominant roles of mRNA stabilization for genes functioning in protein degradation, and adjustment of both transcription and mRNA turnover during the adaptation to stress. We also show that genes regulated independently of the bZIP transcription factor Atf1p are predominantly controlled by mRNA turnover, and identify putative cis-regulatory sequences that are associated with different gene expression strategies during the stress response. This study highlights the intricate and multi-faceted interplay between transcription and RNA turnover during the dynamic regulatory response to stress. |
format | Online Article Text |
id | pubmed-4156502 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Landes Bioscience |
record_format | MEDLINE/PubMed |
spelling | pubmed-41565022015-06-01 Contributions of transcription and mRNA decay to gene expression dynamics of fission yeast in response to oxidative stress Marguerat, Samuel Lawler, Katherine Brazma, Alvis Bähler, Jürg RNA Biol Research Paper The cooperation of transcriptional and post-transcriptional levels of control to shape gene regulation is only partially understood. Here we show that a combination of two simple and non-invasive genomic techniques, coupled with kinetic mathematical modeling, affords insight into the intricate dynamics of RNA regulation in response to oxidative stress in the fission yeast Schizosaccharomyces pombe. This study reveals a dominant role of transcriptional regulation in response to stress, but also points to the first minutes after stress induction as a critical time when the coordinated control of mRNA turnover can support the control of transcription for rapid gene regulation. In addition, we uncover specialized gene expression strategies associated with distinct functional gene groups, such as simultaneous transcriptional repression and mRNA destabilization for genes encoding ribosomal proteins, delayed mRNA destabilization with varying contribution of transcription for ribosome biogenesis genes, dominant roles of mRNA stabilization for genes functioning in protein degradation, and adjustment of both transcription and mRNA turnover during the adaptation to stress. We also show that genes regulated independently of the bZIP transcription factor Atf1p are predominantly controlled by mRNA turnover, and identify putative cis-regulatory sequences that are associated with different gene expression strategies during the stress response. This study highlights the intricate and multi-faceted interplay between transcription and RNA turnover during the dynamic regulatory response to stress. Landes Bioscience 2014-06-01 2014-07-09 /pmc/articles/PMC4156502/ /pubmed/25007214 http://dx.doi.org/10.4161/rna.29196 Text en Copyright © 2014 Landes Bioscience http://creativecommons.org/licenses/by/3.0/ This is an open-access article licensed under a Creative Commons Attribution 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited. |
spellingShingle | Research Paper Marguerat, Samuel Lawler, Katherine Brazma, Alvis Bähler, Jürg Contributions of transcription and mRNA decay to gene expression dynamics of fission yeast in response to oxidative stress |
title | Contributions of transcription and mRNA decay to gene expression dynamics of fission yeast in response to oxidative stress |
title_full | Contributions of transcription and mRNA decay to gene expression dynamics of fission yeast in response to oxidative stress |
title_fullStr | Contributions of transcription and mRNA decay to gene expression dynamics of fission yeast in response to oxidative stress |
title_full_unstemmed | Contributions of transcription and mRNA decay to gene expression dynamics of fission yeast in response to oxidative stress |
title_short | Contributions of transcription and mRNA decay to gene expression dynamics of fission yeast in response to oxidative stress |
title_sort | contributions of transcription and mrna decay to gene expression dynamics of fission yeast in response to oxidative stress |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4156502/ https://www.ncbi.nlm.nih.gov/pubmed/25007214 http://dx.doi.org/10.4161/rna.29196 |
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