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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...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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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. |
format | Online Article Text |
id | pubmed-10345090 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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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