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Two different epigenetic information channels in wild three-spined sticklebacks are involved in salinity adaptation

Epigenetic inheritance has been proposed to contribute to adaptation and acclimation via two information channels: (i) inducible epigenetic marks that enable transgenerational plasticity and (ii) noninducible epigenetic marks resulting from random epimutations shaped by selection. We studied both po...

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Autores principales: Heckwolf, Melanie J., Meyer, Britta S., Häsler, Robert, Höppner, Marc P., Eizaguirre, Christophe, Reusch, Thorsten B. H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7083608/
https://www.ncbi.nlm.nih.gov/pubmed/32219167
http://dx.doi.org/10.1126/sciadv.aaz1138
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author Heckwolf, Melanie J.
Meyer, Britta S.
Häsler, Robert
Höppner, Marc P.
Eizaguirre, Christophe
Reusch, Thorsten B. H.
author_facet Heckwolf, Melanie J.
Meyer, Britta S.
Häsler, Robert
Höppner, Marc P.
Eizaguirre, Christophe
Reusch, Thorsten B. H.
author_sort Heckwolf, Melanie J.
collection PubMed
description Epigenetic inheritance has been proposed to contribute to adaptation and acclimation via two information channels: (i) inducible epigenetic marks that enable transgenerational plasticity and (ii) noninducible epigenetic marks resulting from random epimutations shaped by selection. We studied both postulated channels by sequencing methylomes and genomes of Baltic three-spined sticklebacks (Gasterosteus aculeatus) along a salinity cline. Wild populations differing in salinity tolerance revealed differential methylation (pop-DMS) at genes enriched for osmoregulatory processes. A two-generation experiment demonstrated that 62% of these pop-DMS were noninducible by salinity manipulation, suggesting that they are the result of either direct selection or associated genomic divergence at cis- or trans-regulatory sites. Two-thirds of the remaining inducible pop-DMS increased in similarity to patterns detected in wild populations from corresponding salinities. The level of similarity accentuated over consecutive generations, indicating a mechanism of transgenerational plasticity. While we can attribute natural DNA methylation patterns to the two information channels, their interplay with genomic variation in salinity adaptation is still unresolved.
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spelling pubmed-70836082020-03-26 Two different epigenetic information channels in wild three-spined sticklebacks are involved in salinity adaptation Heckwolf, Melanie J. Meyer, Britta S. Häsler, Robert Höppner, Marc P. Eizaguirre, Christophe Reusch, Thorsten B. H. Sci Adv Research Articles Epigenetic inheritance has been proposed to contribute to adaptation and acclimation via two information channels: (i) inducible epigenetic marks that enable transgenerational plasticity and (ii) noninducible epigenetic marks resulting from random epimutations shaped by selection. We studied both postulated channels by sequencing methylomes and genomes of Baltic three-spined sticklebacks (Gasterosteus aculeatus) along a salinity cline. Wild populations differing in salinity tolerance revealed differential methylation (pop-DMS) at genes enriched for osmoregulatory processes. A two-generation experiment demonstrated that 62% of these pop-DMS were noninducible by salinity manipulation, suggesting that they are the result of either direct selection or associated genomic divergence at cis- or trans-regulatory sites. Two-thirds of the remaining inducible pop-DMS increased in similarity to patterns detected in wild populations from corresponding salinities. The level of similarity accentuated over consecutive generations, indicating a mechanism of transgenerational plasticity. While we can attribute natural DNA methylation patterns to the two information channels, their interplay with genomic variation in salinity adaptation is still unresolved. American Association for the Advancement of Science 2020-03-20 /pmc/articles/PMC7083608/ /pubmed/32219167 http://dx.doi.org/10.1126/sciadv.aaz1138 Text en Copyright © 2020 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 License 4.0 (CC BY). http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Heckwolf, Melanie J.
Meyer, Britta S.
Häsler, Robert
Höppner, Marc P.
Eizaguirre, Christophe
Reusch, Thorsten B. H.
Two different epigenetic information channels in wild three-spined sticklebacks are involved in salinity adaptation
title Two different epigenetic information channels in wild three-spined sticklebacks are involved in salinity adaptation
title_full Two different epigenetic information channels in wild three-spined sticklebacks are involved in salinity adaptation
title_fullStr Two different epigenetic information channels in wild three-spined sticklebacks are involved in salinity adaptation
title_full_unstemmed Two different epigenetic information channels in wild three-spined sticklebacks are involved in salinity adaptation
title_short Two different epigenetic information channels in wild three-spined sticklebacks are involved in salinity adaptation
title_sort two different epigenetic information channels in wild three-spined sticklebacks are involved in salinity adaptation
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7083608/
https://www.ncbi.nlm.nih.gov/pubmed/32219167
http://dx.doi.org/10.1126/sciadv.aaz1138
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