Cargando…

Between-Generation Phenotypic and Epigenetic Stability in a Clonal Snail

Epigenetic variation might play an important role in generating adaptive phenotypes by underpinning within-generation developmental plasticity, persistent parental effects of the environment (e.g., transgenerational plasticity), or heritable epigenetically based polymorphism. These adaptive mechanis...

Descripción completa

Detalles Bibliográficos
Autores principales: Smithson, Mark, Thorson, Jennifer L M, Sadler-Riggleman, Ingrid, Beck, Daniel, Skinner, Michael K, Dybdahl, Mark
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7513791/
https://www.ncbi.nlm.nih.gov/pubmed/32877512
http://dx.doi.org/10.1093/gbe/evaa181
_version_ 1783586453065826304
author Smithson, Mark
Thorson, Jennifer L M
Sadler-Riggleman, Ingrid
Beck, Daniel
Skinner, Michael K
Dybdahl, Mark
author_facet Smithson, Mark
Thorson, Jennifer L M
Sadler-Riggleman, Ingrid
Beck, Daniel
Skinner, Michael K
Dybdahl, Mark
author_sort Smithson, Mark
collection PubMed
description Epigenetic variation might play an important role in generating adaptive phenotypes by underpinning within-generation developmental plasticity, persistent parental effects of the environment (e.g., transgenerational plasticity), or heritable epigenetically based polymorphism. These adaptive mechanisms should be most critical in organisms where genetic sources of variation are limited. Using a clonally reproducing freshwater snail (Potamopyrgus antipodarum), we examined the stability of an adaptive phenotype (shell shape) and of DNA methylation between generations. First, we raised three generations of snails adapted to river currents in the lab without current. We showed that habitat-specific adaptive shell shape was relatively stable across three generations but shifted slightly over generations two and three toward a no-current lake phenotype. We also showed that DNA methylation specific to high-current environments was stable across one generation. This study provides the first evidence of stability of DNA methylation patterns across one generation in an asexual animal. Together, our observations are consistent with the hypothesis that adaptive shell shape variation is at least in part determined by transgenerational plasticity, and that DNA methylation provides a potential mechanism for stability of shell shape across one generation.
format Online
Article
Text
id pubmed-7513791
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-75137912020-09-30 Between-Generation Phenotypic and Epigenetic Stability in a Clonal Snail Smithson, Mark Thorson, Jennifer L M Sadler-Riggleman, Ingrid Beck, Daniel Skinner, Michael K Dybdahl, Mark Genome Biol Evol Research Article Epigenetic variation might play an important role in generating adaptive phenotypes by underpinning within-generation developmental plasticity, persistent parental effects of the environment (e.g., transgenerational plasticity), or heritable epigenetically based polymorphism. These adaptive mechanisms should be most critical in organisms where genetic sources of variation are limited. Using a clonally reproducing freshwater snail (Potamopyrgus antipodarum), we examined the stability of an adaptive phenotype (shell shape) and of DNA methylation between generations. First, we raised three generations of snails adapted to river currents in the lab without current. We showed that habitat-specific adaptive shell shape was relatively stable across three generations but shifted slightly over generations two and three toward a no-current lake phenotype. We also showed that DNA methylation specific to high-current environments was stable across one generation. This study provides the first evidence of stability of DNA methylation patterns across one generation in an asexual animal. Together, our observations are consistent with the hypothesis that adaptive shell shape variation is at least in part determined by transgenerational plasticity, and that DNA methylation provides a potential mechanism for stability of shell shape across one generation. Oxford University Press 2020-09-02 /pmc/articles/PMC7513791/ /pubmed/32877512 http://dx.doi.org/10.1093/gbe/evaa181 Text en © The Author(s) 2020. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. 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 reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Smithson, Mark
Thorson, Jennifer L M
Sadler-Riggleman, Ingrid
Beck, Daniel
Skinner, Michael K
Dybdahl, Mark
Between-Generation Phenotypic and Epigenetic Stability in a Clonal Snail
title Between-Generation Phenotypic and Epigenetic Stability in a Clonal Snail
title_full Between-Generation Phenotypic and Epigenetic Stability in a Clonal Snail
title_fullStr Between-Generation Phenotypic and Epigenetic Stability in a Clonal Snail
title_full_unstemmed Between-Generation Phenotypic and Epigenetic Stability in a Clonal Snail
title_short Between-Generation Phenotypic and Epigenetic Stability in a Clonal Snail
title_sort between-generation phenotypic and epigenetic stability in a clonal snail
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7513791/
https://www.ncbi.nlm.nih.gov/pubmed/32877512
http://dx.doi.org/10.1093/gbe/evaa181
work_keys_str_mv AT smithsonmark betweengenerationphenotypicandepigeneticstabilityinaclonalsnail
AT thorsonjenniferlm betweengenerationphenotypicandepigeneticstabilityinaclonalsnail
AT sadlerrigglemaningrid betweengenerationphenotypicandepigeneticstabilityinaclonalsnail
AT beckdaniel betweengenerationphenotypicandepigeneticstabilityinaclonalsnail
AT skinnermichaelk betweengenerationphenotypicandepigeneticstabilityinaclonalsnail
AT dybdahlmark betweengenerationphenotypicandepigeneticstabilityinaclonalsnail