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The Seagrass Methylome Is Associated With Variation in Photosynthetic Performance Among Clonal Shoots

Evolutionary theory predicts that clonal organisms are more susceptible to extinction than sexually reproducing organisms, due to low genetic variation and slow rates of evolution. In agreement, conservation management considers genetic variation as the ultimate measure of a population’s ability to...

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Autores principales: Jueterbock, Alexander, Boström, Christoffer, Coyer, James A., Olsen, Jeanine L., Kopp, Martina, Dhanasiri, Anusha K. S., Smolina, Irina, Arnaud-Haond, Sophie, Van de Peer, Yves, Hoarau, Galice
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7498905/
https://www.ncbi.nlm.nih.gov/pubmed/33013993
http://dx.doi.org/10.3389/fpls.2020.571646
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author Jueterbock, Alexander
Boström, Christoffer
Coyer, James A.
Olsen, Jeanine L.
Kopp, Martina
Dhanasiri, Anusha K. S.
Smolina, Irina
Arnaud-Haond, Sophie
Van de Peer, Yves
Hoarau, Galice
author_facet Jueterbock, Alexander
Boström, Christoffer
Coyer, James A.
Olsen, Jeanine L.
Kopp, Martina
Dhanasiri, Anusha K. S.
Smolina, Irina
Arnaud-Haond, Sophie
Van de Peer, Yves
Hoarau, Galice
author_sort Jueterbock, Alexander
collection PubMed
description Evolutionary theory predicts that clonal organisms are more susceptible to extinction than sexually reproducing organisms, due to low genetic variation and slow rates of evolution. In agreement, conservation management considers genetic variation as the ultimate measure of a population’s ability to survive over time. However, clonal plants are among the oldest living organisms on our planet. Here, we test the hypothesis that clonal seagrass meadows display epigenetic variation that complements genetic variation as a source of phenotypic variation. In a clonal meadow of the seagrass Zostera marina, we characterized DNA methylation among 42 shoots. We also sequenced the whole genome of 10 shoots to correlate methylation patterns with photosynthetic performance under exposure to and recovery from 27°C, while controlling for somatic mutations. Here, we show for the first time that clonal seagrass shoots display DNA methylation variation that is independent from underlying genetic variation, and associated with variation in photosynthetic performance under experimental conditions. It remains unknown to what degree this association could be influenced by epigenetic responses to transplantation-related stress, given that the methylomes showed a strong shift under acclimation to laboratory conditions. The lack of untreated control samples in the heat stress experiment did not allow us to distinguish methylome shifts induced by acclimation from such induced by heat stress. Notwithstanding, the co-variation in DNA methylation and photosynthetic performance may be linked via gene expression because methylation patterns varied in functionally relevant genes involved in photosynthesis, and in the repair and prevention of heat-induced protein damage. While genotypic diversity has been shown to enhance stress resilience in seagrass meadows, we suggest that epigenetic variation plays a similar role in meadows dominated by a single genotype. Consequently, conservation management of clonal plants should consider epigenetic variation as indicator of resilience and stability.
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spelling pubmed-74989052020-10-02 The Seagrass Methylome Is Associated With Variation in Photosynthetic Performance Among Clonal Shoots Jueterbock, Alexander Boström, Christoffer Coyer, James A. Olsen, Jeanine L. Kopp, Martina Dhanasiri, Anusha K. S. Smolina, Irina Arnaud-Haond, Sophie Van de Peer, Yves Hoarau, Galice Front Plant Sci Plant Science Evolutionary theory predicts that clonal organisms are more susceptible to extinction than sexually reproducing organisms, due to low genetic variation and slow rates of evolution. In agreement, conservation management considers genetic variation as the ultimate measure of a population’s ability to survive over time. However, clonal plants are among the oldest living organisms on our planet. Here, we test the hypothesis that clonal seagrass meadows display epigenetic variation that complements genetic variation as a source of phenotypic variation. In a clonal meadow of the seagrass Zostera marina, we characterized DNA methylation among 42 shoots. We also sequenced the whole genome of 10 shoots to correlate methylation patterns with photosynthetic performance under exposure to and recovery from 27°C, while controlling for somatic mutations. Here, we show for the first time that clonal seagrass shoots display DNA methylation variation that is independent from underlying genetic variation, and associated with variation in photosynthetic performance under experimental conditions. It remains unknown to what degree this association could be influenced by epigenetic responses to transplantation-related stress, given that the methylomes showed a strong shift under acclimation to laboratory conditions. The lack of untreated control samples in the heat stress experiment did not allow us to distinguish methylome shifts induced by acclimation from such induced by heat stress. Notwithstanding, the co-variation in DNA methylation and photosynthetic performance may be linked via gene expression because methylation patterns varied in functionally relevant genes involved in photosynthesis, and in the repair and prevention of heat-induced protein damage. While genotypic diversity has been shown to enhance stress resilience in seagrass meadows, we suggest that epigenetic variation plays a similar role in meadows dominated by a single genotype. Consequently, conservation management of clonal plants should consider epigenetic variation as indicator of resilience and stability. Frontiers Media S.A. 2020-09-04 /pmc/articles/PMC7498905/ /pubmed/33013993 http://dx.doi.org/10.3389/fpls.2020.571646 Text en Copyright © 2020 Jueterbock, Boström, Coyer, Olsen, Kopp, Dhanasiri, Smolina, Arnaud-Haond, Van de Peer and Hoarau http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Plant Science
Jueterbock, Alexander
Boström, Christoffer
Coyer, James A.
Olsen, Jeanine L.
Kopp, Martina
Dhanasiri, Anusha K. S.
Smolina, Irina
Arnaud-Haond, Sophie
Van de Peer, Yves
Hoarau, Galice
The Seagrass Methylome Is Associated With Variation in Photosynthetic Performance Among Clonal Shoots
title The Seagrass Methylome Is Associated With Variation in Photosynthetic Performance Among Clonal Shoots
title_full The Seagrass Methylome Is Associated With Variation in Photosynthetic Performance Among Clonal Shoots
title_fullStr The Seagrass Methylome Is Associated With Variation in Photosynthetic Performance Among Clonal Shoots
title_full_unstemmed The Seagrass Methylome Is Associated With Variation in Photosynthetic Performance Among Clonal Shoots
title_short The Seagrass Methylome Is Associated With Variation in Photosynthetic Performance Among Clonal Shoots
title_sort seagrass methylome is associated with variation in photosynthetic performance among clonal shoots
topic Plant Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7498905/
https://www.ncbi.nlm.nih.gov/pubmed/33013993
http://dx.doi.org/10.3389/fpls.2020.571646
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