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Phosphoproteome dynamics of Saccharomyces cerevisiae under heat shock and cold stress

The ability of cells and organisms to survive and function through changes in temperature evolved from their specific adaptations to nonoptimal growth conditions. Responses to elevated temperatures have been studied in yeast and other model organisms using transcriptome profiling and provided valuab...

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Autores principales: Kanshin, Evgeny, Kubiniok, Peter, Thattikota, Yogitha, D'Amours, Damien, Thibault, Pierre
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BlackWell Publishing Ltd 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4501848/
https://www.ncbi.nlm.nih.gov/pubmed/26040289
http://dx.doi.org/10.15252/msb.20156170
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author Kanshin, Evgeny
Kubiniok, Peter
Thattikota, Yogitha
D'Amours, Damien
Thibault, Pierre
author_facet Kanshin, Evgeny
Kubiniok, Peter
Thattikota, Yogitha
D'Amours, Damien
Thibault, Pierre
author_sort Kanshin, Evgeny
collection PubMed
description The ability of cells and organisms to survive and function through changes in temperature evolved from their specific adaptations to nonoptimal growth conditions. Responses to elevated temperatures have been studied in yeast and other model organisms using transcriptome profiling and provided valuable biological insights on molecular mechanisms involved in stress tolerance and adaptation to adverse environment. In contrast, little is known about rapid signaling events associated with changes in temperature. To gain a better understanding of global changes in protein phosphorylation in response to heat and cold, we developed a high temporal resolution phosphoproteomics protocol to study cell signaling in Saccharomyces cerevisiae. The method allowed for quantitative analysis of phosphodynamics on 2,777 phosphosites from 1,228 proteins. The correlation of kinetic profiles between kinases and their substrates provided a predictive tool to identify new putative substrates for kinases such as Cdc28 and PKA. Cell cycle analyses revealed that the increased phosphorylation of Cdc28 at its inhibitory site Y19 during heat shock is an adaptive response that delays cell cycle progression under stress conditions. The cellular responses to heat and cold were associated with extensive changes in phosphorylation on proteins implicated in transcription, protein folding and degradation, cell cycle regulation and morphogenesis.
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spelling pubmed-45018482015-07-21 Phosphoproteome dynamics of Saccharomyces cerevisiae under heat shock and cold stress Kanshin, Evgeny Kubiniok, Peter Thattikota, Yogitha D'Amours, Damien Thibault, Pierre Mol Syst Biol Articles The ability of cells and organisms to survive and function through changes in temperature evolved from their specific adaptations to nonoptimal growth conditions. Responses to elevated temperatures have been studied in yeast and other model organisms using transcriptome profiling and provided valuable biological insights on molecular mechanisms involved in stress tolerance and adaptation to adverse environment. In contrast, little is known about rapid signaling events associated with changes in temperature. To gain a better understanding of global changes in protein phosphorylation in response to heat and cold, we developed a high temporal resolution phosphoproteomics protocol to study cell signaling in Saccharomyces cerevisiae. The method allowed for quantitative analysis of phosphodynamics on 2,777 phosphosites from 1,228 proteins. The correlation of kinetic profiles between kinases and their substrates provided a predictive tool to identify new putative substrates for kinases such as Cdc28 and PKA. Cell cycle analyses revealed that the increased phosphorylation of Cdc28 at its inhibitory site Y19 during heat shock is an adaptive response that delays cell cycle progression under stress conditions. The cellular responses to heat and cold were associated with extensive changes in phosphorylation on proteins implicated in transcription, protein folding and degradation, cell cycle regulation and morphogenesis. BlackWell Publishing Ltd 2015-06-03 /pmc/articles/PMC4501848/ /pubmed/26040289 http://dx.doi.org/10.15252/msb.20156170 Text en © 2015 The Authors. Published under the terms of the CC BY 4.0 license http://creativecommons.org/licenses/by/4.0/ This is an open access article under the terms of the Creative Commons Attribution 4.0 License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Articles
Kanshin, Evgeny
Kubiniok, Peter
Thattikota, Yogitha
D'Amours, Damien
Thibault, Pierre
Phosphoproteome dynamics of Saccharomyces cerevisiae under heat shock and cold stress
title Phosphoproteome dynamics of Saccharomyces cerevisiae under heat shock and cold stress
title_full Phosphoproteome dynamics of Saccharomyces cerevisiae under heat shock and cold stress
title_fullStr Phosphoproteome dynamics of Saccharomyces cerevisiae under heat shock and cold stress
title_full_unstemmed Phosphoproteome dynamics of Saccharomyces cerevisiae under heat shock and cold stress
title_short Phosphoproteome dynamics of Saccharomyces cerevisiae under heat shock and cold stress
title_sort phosphoproteome dynamics of saccharomyces cerevisiae under heat shock and cold stress
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4501848/
https://www.ncbi.nlm.nih.gov/pubmed/26040289
http://dx.doi.org/10.15252/msb.20156170
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