Cargando…
Environmental stresses induce transgenerationally inheritable survival advantages via germline-to-soma communication in Caenorhabditis elegans
Hormesis is a biological phenomenon, whereby exposure to low levels of toxic agents or conditions increases organismal viability. It thus represents a beneficial aspect of adaptive responses to harmful environmental stimuli. Here we show that hormesis effects induced in the parental generation can b...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5227915/ https://www.ncbi.nlm.nih.gov/pubmed/28067237 http://dx.doi.org/10.1038/ncomms14031 |
_version_ | 1782493896485371904 |
---|---|
author | Kishimoto, Saya Uno, Masaharu Okabe, Emiko Nono, Masanori Nishida, Eisuke |
author_facet | Kishimoto, Saya Uno, Masaharu Okabe, Emiko Nono, Masanori Nishida, Eisuke |
author_sort | Kishimoto, Saya |
collection | PubMed |
description | Hormesis is a biological phenomenon, whereby exposure to low levels of toxic agents or conditions increases organismal viability. It thus represents a beneficial aspect of adaptive responses to harmful environmental stimuli. Here we show that hormesis effects induced in the parental generation can be passed on to the descendants in Caenorhabditis elegans. Animals subjected to various stressors during developmental stages exhibit increased resistance to oxidative stress and proteotoxicity. The increased resistance is transmitted to the subsequent generations grown under unstressed conditions through epigenetic alterations. Our analysis reveal that the insulin/insulin-like growth factor (IGF) signalling effector DAF-16/FOXO and the heat-shock factor HSF-1 in the parental somatic cells mediate the formation of epigenetic memory, which is maintained through the histone H3 lysine 4 trimethylase complex in the germline across generations. The elicitation of memory requires the transcription factor SKN-1/Nrf in somatic tissues. We propose that germ-to-soma communication across generations is an essential framework for the transgenerational inheritance of acquired traits, which provides the offspring with survival advantages to deal with environmental perturbation. |
format | Online Article Text |
id | pubmed-5227915 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-52279152017-02-01 Environmental stresses induce transgenerationally inheritable survival advantages via germline-to-soma communication in Caenorhabditis elegans Kishimoto, Saya Uno, Masaharu Okabe, Emiko Nono, Masanori Nishida, Eisuke Nat Commun Article Hormesis is a biological phenomenon, whereby exposure to low levels of toxic agents or conditions increases organismal viability. It thus represents a beneficial aspect of adaptive responses to harmful environmental stimuli. Here we show that hormesis effects induced in the parental generation can be passed on to the descendants in Caenorhabditis elegans. Animals subjected to various stressors during developmental stages exhibit increased resistance to oxidative stress and proteotoxicity. The increased resistance is transmitted to the subsequent generations grown under unstressed conditions through epigenetic alterations. Our analysis reveal that the insulin/insulin-like growth factor (IGF) signalling effector DAF-16/FOXO and the heat-shock factor HSF-1 in the parental somatic cells mediate the formation of epigenetic memory, which is maintained through the histone H3 lysine 4 trimethylase complex in the germline across generations. The elicitation of memory requires the transcription factor SKN-1/Nrf in somatic tissues. We propose that germ-to-soma communication across generations is an essential framework for the transgenerational inheritance of acquired traits, which provides the offspring with survival advantages to deal with environmental perturbation. Nature Publishing Group 2017-01-09 /pmc/articles/PMC5227915/ /pubmed/28067237 http://dx.doi.org/10.1038/ncomms14031 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Kishimoto, Saya Uno, Masaharu Okabe, Emiko Nono, Masanori Nishida, Eisuke Environmental stresses induce transgenerationally inheritable survival advantages via germline-to-soma communication in Caenorhabditis elegans |
title | Environmental stresses induce transgenerationally inheritable survival advantages via germline-to-soma communication in Caenorhabditis elegans |
title_full | Environmental stresses induce transgenerationally inheritable survival advantages via germline-to-soma communication in Caenorhabditis elegans |
title_fullStr | Environmental stresses induce transgenerationally inheritable survival advantages via germline-to-soma communication in Caenorhabditis elegans |
title_full_unstemmed | Environmental stresses induce transgenerationally inheritable survival advantages via germline-to-soma communication in Caenorhabditis elegans |
title_short | Environmental stresses induce transgenerationally inheritable survival advantages via germline-to-soma communication in Caenorhabditis elegans |
title_sort | environmental stresses induce transgenerationally inheritable survival advantages via germline-to-soma communication in caenorhabditis elegans |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5227915/ https://www.ncbi.nlm.nih.gov/pubmed/28067237 http://dx.doi.org/10.1038/ncomms14031 |
work_keys_str_mv | AT kishimotosaya environmentalstressesinducetransgenerationallyinheritablesurvivaladvantagesviagermlinetosomacommunicationincaenorhabditiselegans AT unomasaharu environmentalstressesinducetransgenerationallyinheritablesurvivaladvantagesviagermlinetosomacommunicationincaenorhabditiselegans AT okabeemiko environmentalstressesinducetransgenerationallyinheritablesurvivaladvantagesviagermlinetosomacommunicationincaenorhabditiselegans AT nonomasanori environmentalstressesinducetransgenerationallyinheritablesurvivaladvantagesviagermlinetosomacommunicationincaenorhabditiselegans AT nishidaeisuke environmentalstressesinducetransgenerationallyinheritablesurvivaladvantagesviagermlinetosomacommunicationincaenorhabditiselegans |