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Parental energy-sensing pathways control intergenerational offspring sex determination in the nematode Auanema freiburgensis

BACKGROUND: Environmental stimuli experienced by the parental generation influence the phenotype of subsequent generations (Demoinet et al., Proc Natl Acad Sci U S A 114:E2689-E2698, 2017; Burton et al., Nat Cell Biol 19:252–257, 2017; Agrawal et al., Nature 401:60-63, 1999). The effects of these st...

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Autores principales: Robles, Pedro, Turner, Anisa, Zuco, Giusy, Adams, Sally, Paganopolou, Panagiota, Winton, Michael, Hill, Beth, Kache, Vikas, Bateson, Christine, Pires-daSilva, Andre
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8130380/
https://www.ncbi.nlm.nih.gov/pubmed/34001117
http://dx.doi.org/10.1186/s12915-021-01032-1
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author Robles, Pedro
Turner, Anisa
Zuco, Giusy
Adams, Sally
Paganopolou, Panagiota
Winton, Michael
Hill, Beth
Kache, Vikas
Bateson, Christine
Pires-daSilva, Andre
author_facet Robles, Pedro
Turner, Anisa
Zuco, Giusy
Adams, Sally
Paganopolou, Panagiota
Winton, Michael
Hill, Beth
Kache, Vikas
Bateson, Christine
Pires-daSilva, Andre
author_sort Robles, Pedro
collection PubMed
description BACKGROUND: Environmental stimuli experienced by the parental generation influence the phenotype of subsequent generations (Demoinet et al., Proc Natl Acad Sci U S A 114:E2689-E2698, 2017; Burton et al., Nat Cell Biol 19:252–257, 2017; Agrawal et al., Nature 401:60-63, 1999). The effects of these stimuli on the parental generation may be passed through the germline, but the mechanisms at the basis of this non-Mendelian type of inheritance, their level of conservation, how they lead to adaptive vs non-adaptive, and intergenerational vs transgenerational inheritance are poorly understood. Here we show that modulation of nutrient-sensing pathways in the parental generation of the nematode Auanema freiburgensis regulates phenotypic plasticity of its offspring. RESULTS: In response to con-specific pheromones indicative of stress, AMP-activated protein kinase (AMPK), mechanistic target of rapamycin complex 1 (mTORC1), and insulin signaling regulate stress resistance and sex determination across one generation, and these effects can be mimicked by pathway modulators. The effectors of these pathways are closely associated with the chromatin, and their regulation affects the chromatin acetylation status in the germline. CONCLUSION: These results suggest that highly conserved metabolic sensors regulate phenotypic plasticity through regulation of subcellular localization of their effectors, leading to changes in chromatin acetylation and epigenetic status of the germline. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12915-021-01032-1.
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spelling pubmed-81303802021-05-18 Parental energy-sensing pathways control intergenerational offspring sex determination in the nematode Auanema freiburgensis Robles, Pedro Turner, Anisa Zuco, Giusy Adams, Sally Paganopolou, Panagiota Winton, Michael Hill, Beth Kache, Vikas Bateson, Christine Pires-daSilva, Andre BMC Biol Research Article BACKGROUND: Environmental stimuli experienced by the parental generation influence the phenotype of subsequent generations (Demoinet et al., Proc Natl Acad Sci U S A 114:E2689-E2698, 2017; Burton et al., Nat Cell Biol 19:252–257, 2017; Agrawal et al., Nature 401:60-63, 1999). The effects of these stimuli on the parental generation may be passed through the germline, but the mechanisms at the basis of this non-Mendelian type of inheritance, their level of conservation, how they lead to adaptive vs non-adaptive, and intergenerational vs transgenerational inheritance are poorly understood. Here we show that modulation of nutrient-sensing pathways in the parental generation of the nematode Auanema freiburgensis regulates phenotypic plasticity of its offspring. RESULTS: In response to con-specific pheromones indicative of stress, AMP-activated protein kinase (AMPK), mechanistic target of rapamycin complex 1 (mTORC1), and insulin signaling regulate stress resistance and sex determination across one generation, and these effects can be mimicked by pathway modulators. The effectors of these pathways are closely associated with the chromatin, and their regulation affects the chromatin acetylation status in the germline. CONCLUSION: These results suggest that highly conserved metabolic sensors regulate phenotypic plasticity through regulation of subcellular localization of their effectors, leading to changes in chromatin acetylation and epigenetic status of the germline. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12915-021-01032-1. BioMed Central 2021-05-17 /pmc/articles/PMC8130380/ /pubmed/34001117 http://dx.doi.org/10.1186/s12915-021-01032-1 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
Robles, Pedro
Turner, Anisa
Zuco, Giusy
Adams, Sally
Paganopolou, Panagiota
Winton, Michael
Hill, Beth
Kache, Vikas
Bateson, Christine
Pires-daSilva, Andre
Parental energy-sensing pathways control intergenerational offspring sex determination in the nematode Auanema freiburgensis
title Parental energy-sensing pathways control intergenerational offspring sex determination in the nematode Auanema freiburgensis
title_full Parental energy-sensing pathways control intergenerational offspring sex determination in the nematode Auanema freiburgensis
title_fullStr Parental energy-sensing pathways control intergenerational offspring sex determination in the nematode Auanema freiburgensis
title_full_unstemmed Parental energy-sensing pathways control intergenerational offspring sex determination in the nematode Auanema freiburgensis
title_short Parental energy-sensing pathways control intergenerational offspring sex determination in the nematode Auanema freiburgensis
title_sort parental energy-sensing pathways control intergenerational offspring sex determination in the nematode auanema freiburgensis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8130380/
https://www.ncbi.nlm.nih.gov/pubmed/34001117
http://dx.doi.org/10.1186/s12915-021-01032-1
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