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N(6)-methyldeoxyadenine and histone methylation mediate transgenerational survival advantages induced by hormetic heat stress

Environmental stress can induce survival advantages that are passed down to multiple generations, representing an evolutionarily advantageous adaptation at the species level. Using the nematode worm Caenorhabditis elegans as a model, we found that heat shock experienced in either parent could increa...

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Autores principales: Wan, Qin-Li, Meng, Xiao, Dai, Wenyu, Luo, Zhenhuan, Wang, Chongyang, Fu, Xiaodie, Yang, Jing, Ye, Qunshan, Zhou, Qinghua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7775758/
https://www.ncbi.nlm.nih.gov/pubmed/33523838
http://dx.doi.org/10.1126/sciadv.abc3026
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author Wan, Qin-Li
Meng, Xiao
Dai, Wenyu
Luo, Zhenhuan
Wang, Chongyang
Fu, Xiaodie
Yang, Jing
Ye, Qunshan
Zhou, Qinghua
author_facet Wan, Qin-Li
Meng, Xiao
Dai, Wenyu
Luo, Zhenhuan
Wang, Chongyang
Fu, Xiaodie
Yang, Jing
Ye, Qunshan
Zhou, Qinghua
author_sort Wan, Qin-Li
collection PubMed
description Environmental stress can induce survival advantages that are passed down to multiple generations, representing an evolutionarily advantageous adaptation at the species level. Using the nematode worm Caenorhabditis elegans as a model, we found that heat shock experienced in either parent could increase the longevity of themselves and up to the fifth generation of descendants. Mechanistic analyses revealed that transcription factor DAF-16/FOXO, heat shock factor HSF-1, and nuclear receptor DAF-12/FXR functioned transgenerationally to implement the hormetic stress response. Histone H3K9me3 methyltransferases SET-25 and SET-32 and DNA N(6)-methyl methyltransferase DAMT-1 participated in transmitting high-temperature memory across generations. H3K9me3 and N(6)-methyladenine could mark heat stress response genes and promote their transcription in progeny to extend life span. We dissected the mechanisms responsible for implementing and transmitting environmental memories in descendants from heat-shocked parents and demonstrated that hormetic stress caused survival benefits could be transmitted to multiple generations through H3K9me3 and N(6)-mA modifications.
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spelling pubmed-77757582021-01-14 N(6)-methyldeoxyadenine and histone methylation mediate transgenerational survival advantages induced by hormetic heat stress Wan, Qin-Li Meng, Xiao Dai, Wenyu Luo, Zhenhuan Wang, Chongyang Fu, Xiaodie Yang, Jing Ye, Qunshan Zhou, Qinghua Sci Adv Research Articles Environmental stress can induce survival advantages that are passed down to multiple generations, representing an evolutionarily advantageous adaptation at the species level. Using the nematode worm Caenorhabditis elegans as a model, we found that heat shock experienced in either parent could increase the longevity of themselves and up to the fifth generation of descendants. Mechanistic analyses revealed that transcription factor DAF-16/FOXO, heat shock factor HSF-1, and nuclear receptor DAF-12/FXR functioned transgenerationally to implement the hormetic stress response. Histone H3K9me3 methyltransferases SET-25 and SET-32 and DNA N(6)-methyl methyltransferase DAMT-1 participated in transmitting high-temperature memory across generations. H3K9me3 and N(6)-methyladenine could mark heat stress response genes and promote their transcription in progeny to extend life span. We dissected the mechanisms responsible for implementing and transmitting environmental memories in descendants from heat-shocked parents and demonstrated that hormetic stress caused survival benefits could be transmitted to multiple generations through H3K9me3 and N(6)-mA modifications. American Association for the Advancement of Science 2021-01-01 /pmc/articles/PMC7775758/ /pubmed/33523838 http://dx.doi.org/10.1126/sciadv.abc3026 Text en Copyright © 2021 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). https://creativecommons.org/licenses/by-nc/4.0/ https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (https://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited.
spellingShingle Research Articles
Wan, Qin-Li
Meng, Xiao
Dai, Wenyu
Luo, Zhenhuan
Wang, Chongyang
Fu, Xiaodie
Yang, Jing
Ye, Qunshan
Zhou, Qinghua
N(6)-methyldeoxyadenine and histone methylation mediate transgenerational survival advantages induced by hormetic heat stress
title N(6)-methyldeoxyadenine and histone methylation mediate transgenerational survival advantages induced by hormetic heat stress
title_full N(6)-methyldeoxyadenine and histone methylation mediate transgenerational survival advantages induced by hormetic heat stress
title_fullStr N(6)-methyldeoxyadenine and histone methylation mediate transgenerational survival advantages induced by hormetic heat stress
title_full_unstemmed N(6)-methyldeoxyadenine and histone methylation mediate transgenerational survival advantages induced by hormetic heat stress
title_short N(6)-methyldeoxyadenine and histone methylation mediate transgenerational survival advantages induced by hormetic heat stress
title_sort n(6)-methyldeoxyadenine and histone methylation mediate transgenerational survival advantages induced by hormetic heat stress
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7775758/
https://www.ncbi.nlm.nih.gov/pubmed/33523838
http://dx.doi.org/10.1126/sciadv.abc3026
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