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Temporal dynamics of gene expression in heat-stressed Caenorhabditis elegans

There is considerable insight into pathways and genes associated with heat-stress conditions. Most genes involved in stress response have been identified using mutant screens or gene knockdowns. Yet, there is limited understanding of the temporal dynamics of global gene expression in stressful envir...

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Autores principales: Jovic, Katharina, Sterken, Mark G., Grilli, Jacopo, Bevers, Roel P. J., Rodriguez, Miriam, Riksen, Joost A. G., Allesina, Stefano, Kammenga, Jan E., Snoek, L. Basten
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5724892/
https://www.ncbi.nlm.nih.gov/pubmed/29228038
http://dx.doi.org/10.1371/journal.pone.0189445
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author Jovic, Katharina
Sterken, Mark G.
Grilli, Jacopo
Bevers, Roel P. J.
Rodriguez, Miriam
Riksen, Joost A. G.
Allesina, Stefano
Kammenga, Jan E.
Snoek, L. Basten
author_facet Jovic, Katharina
Sterken, Mark G.
Grilli, Jacopo
Bevers, Roel P. J.
Rodriguez, Miriam
Riksen, Joost A. G.
Allesina, Stefano
Kammenga, Jan E.
Snoek, L. Basten
author_sort Jovic, Katharina
collection PubMed
description There is considerable insight into pathways and genes associated with heat-stress conditions. Most genes involved in stress response have been identified using mutant screens or gene knockdowns. Yet, there is limited understanding of the temporal dynamics of global gene expression in stressful environments. Here, we studied global gene expression profiles during 12 hours of heat stress in the nematode C. elegans. Using a high-resolution time series of increasing stress exposures, we found a distinct shift in gene expression patterns between 3–4 hours into the stress response, separating an initially highly dynamic phase from a later relatively stagnant phase. This turning point in expression dynamics coincided with a phenotypic turning point, as shown by a strong decrease in movement, survival and, progeny count in the days following the stress. Both detectable at transcriptional and phenotypic level, this study pin-points a relatively small time frame during heat stress at which enough damage is accumulated, making it impossible to recover the next few days.
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spelling pubmed-57248922017-12-15 Temporal dynamics of gene expression in heat-stressed Caenorhabditis elegans Jovic, Katharina Sterken, Mark G. Grilli, Jacopo Bevers, Roel P. J. Rodriguez, Miriam Riksen, Joost A. G. Allesina, Stefano Kammenga, Jan E. Snoek, L. Basten PLoS One Research Article There is considerable insight into pathways and genes associated with heat-stress conditions. Most genes involved in stress response have been identified using mutant screens or gene knockdowns. Yet, there is limited understanding of the temporal dynamics of global gene expression in stressful environments. Here, we studied global gene expression profiles during 12 hours of heat stress in the nematode C. elegans. Using a high-resolution time series of increasing stress exposures, we found a distinct shift in gene expression patterns between 3–4 hours into the stress response, separating an initially highly dynamic phase from a later relatively stagnant phase. This turning point in expression dynamics coincided with a phenotypic turning point, as shown by a strong decrease in movement, survival and, progeny count in the days following the stress. Both detectable at transcriptional and phenotypic level, this study pin-points a relatively small time frame during heat stress at which enough damage is accumulated, making it impossible to recover the next few days. Public Library of Science 2017-12-11 /pmc/articles/PMC5724892/ /pubmed/29228038 http://dx.doi.org/10.1371/journal.pone.0189445 Text en © 2017 Jovic et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Jovic, Katharina
Sterken, Mark G.
Grilli, Jacopo
Bevers, Roel P. J.
Rodriguez, Miriam
Riksen, Joost A. G.
Allesina, Stefano
Kammenga, Jan E.
Snoek, L. Basten
Temporal dynamics of gene expression in heat-stressed Caenorhabditis elegans
title Temporal dynamics of gene expression in heat-stressed Caenorhabditis elegans
title_full Temporal dynamics of gene expression in heat-stressed Caenorhabditis elegans
title_fullStr Temporal dynamics of gene expression in heat-stressed Caenorhabditis elegans
title_full_unstemmed Temporal dynamics of gene expression in heat-stressed Caenorhabditis elegans
title_short Temporal dynamics of gene expression in heat-stressed Caenorhabditis elegans
title_sort temporal dynamics of gene expression in heat-stressed caenorhabditis elegans
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5724892/
https://www.ncbi.nlm.nih.gov/pubmed/29228038
http://dx.doi.org/10.1371/journal.pone.0189445
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