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Reprogramming of the transcriptome after heat stress mediates heat hormesis in Caenorhabditis elegans

Transient stress experiences not only trigger acute stress responses, but can also have long-lasting effects on cellular functions. In Caenorhabditis elegans, a brief exposure to heat shock during early adulthood extends lifespan and improves stress resistance, a phenomenon known as heat hormesis. H...

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Autores principales: Xu, Fan, Li, Ruoyao, von Gromoff, Erika D., Drepper, Friedel, Knapp, Bettina, Warscheid, Bettina, Baumeister, Ralf, Qi, Wenjing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10345090/
https://www.ncbi.nlm.nih.gov/pubmed/37443152
http://dx.doi.org/10.1038/s41467-023-39882-8
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author Xu, Fan
Li, Ruoyao
von Gromoff, Erika D.
Drepper, Friedel
Knapp, Bettina
Warscheid, Bettina
Baumeister, Ralf
Qi, Wenjing
author_facet Xu, Fan
Li, Ruoyao
von Gromoff, Erika D.
Drepper, Friedel
Knapp, Bettina
Warscheid, Bettina
Baumeister, Ralf
Qi, Wenjing
author_sort Xu, Fan
collection PubMed
description Transient stress experiences not only trigger acute stress responses, but can also have long-lasting effects on cellular functions. In Caenorhabditis elegans, a brief exposure to heat shock during early adulthood extends lifespan and improves stress resistance, a phenomenon known as heat hormesis. Here, we investigated the prolonged effect of hormetic heat stress on the transcriptome of worms and found that the canonical heat shock response is followed by a profound transcriptional reprogramming in the post-stress period. This reprogramming relies on the endoribonuclease ENDU-2 but not the heat shock factor 1. ENDU-2 co-localizes with chromatin and interacts with RNA polymerase II, enabling specific regulation of transcription after the stress period. Failure to activate the post-stress response does not affect the resistance of animals to heat shock but eliminates the beneficial effects of hormetic heat stress. In summary, our work discovers that the RNA-binding protein ENDU-2 mediates the long-term impacts of transient heat stress via reprogramming transcriptome after stress exposure.
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spelling pubmed-103450902023-07-15 Reprogramming of the transcriptome after heat stress mediates heat hormesis in Caenorhabditis elegans Xu, Fan Li, Ruoyao von Gromoff, Erika D. Drepper, Friedel Knapp, Bettina Warscheid, Bettina Baumeister, Ralf Qi, Wenjing Nat Commun Article Transient stress experiences not only trigger acute stress responses, but can also have long-lasting effects on cellular functions. In Caenorhabditis elegans, a brief exposure to heat shock during early adulthood extends lifespan and improves stress resistance, a phenomenon known as heat hormesis. Here, we investigated the prolonged effect of hormetic heat stress on the transcriptome of worms and found that the canonical heat shock response is followed by a profound transcriptional reprogramming in the post-stress period. This reprogramming relies on the endoribonuclease ENDU-2 but not the heat shock factor 1. ENDU-2 co-localizes with chromatin and interacts with RNA polymerase II, enabling specific regulation of transcription after the stress period. Failure to activate the post-stress response does not affect the resistance of animals to heat shock but eliminates the beneficial effects of hormetic heat stress. In summary, our work discovers that the RNA-binding protein ENDU-2 mediates the long-term impacts of transient heat stress via reprogramming transcriptome after stress exposure. Nature Publishing Group UK 2023-07-13 /pmc/articles/PMC10345090/ /pubmed/37443152 http://dx.doi.org/10.1038/s41467-023-39882-8 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Xu, Fan
Li, Ruoyao
von Gromoff, Erika D.
Drepper, Friedel
Knapp, Bettina
Warscheid, Bettina
Baumeister, Ralf
Qi, Wenjing
Reprogramming of the transcriptome after heat stress mediates heat hormesis in Caenorhabditis elegans
title Reprogramming of the transcriptome after heat stress mediates heat hormesis in Caenorhabditis elegans
title_full Reprogramming of the transcriptome after heat stress mediates heat hormesis in Caenorhabditis elegans
title_fullStr Reprogramming of the transcriptome after heat stress mediates heat hormesis in Caenorhabditis elegans
title_full_unstemmed Reprogramming of the transcriptome after heat stress mediates heat hormesis in Caenorhabditis elegans
title_short Reprogramming of the transcriptome after heat stress mediates heat hormesis in Caenorhabditis elegans
title_sort reprogramming of the transcriptome after heat stress mediates heat hormesis in caenorhabditis elegans
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10345090/
https://www.ncbi.nlm.nih.gov/pubmed/37443152
http://dx.doi.org/10.1038/s41467-023-39882-8
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