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Extending the Genotype in Brachypodium by Including DNA Methylation Reveals a Joint Contribution with Genetics on Adaptive Traits

Epigenomic changes have been considered a potential missing link underlying phenotypic variation in quantitative traits but is potentially confounded with the underlying DNA sequence variation. Although the concept of epigenetic inheritance has been discussed in depth, there have been few studies at...

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Autores principales: Eichten, Steven R., Srivastava, Akanksha, Reddiex, Adam J., Ganguly, Diep R., Heussler, Alison, Streich, Jared C., Wilson, Pip B., Borevitz, Justin O.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Genetics Society of America 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7202021/
https://www.ncbi.nlm.nih.gov/pubmed/32132166
http://dx.doi.org/10.1534/g3.120.401189
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author Eichten, Steven R.
Srivastava, Akanksha
Reddiex, Adam J.
Ganguly, Diep R.
Heussler, Alison
Streich, Jared C.
Wilson, Pip B.
Borevitz, Justin O.
author_facet Eichten, Steven R.
Srivastava, Akanksha
Reddiex, Adam J.
Ganguly, Diep R.
Heussler, Alison
Streich, Jared C.
Wilson, Pip B.
Borevitz, Justin O.
author_sort Eichten, Steven R.
collection PubMed
description Epigenomic changes have been considered a potential missing link underlying phenotypic variation in quantitative traits but is potentially confounded with the underlying DNA sequence variation. Although the concept of epigenetic inheritance has been discussed in depth, there have been few studies attempting to directly dissect the amount of epigenomic variation within inbred natural populations while also accounting for genetic diversity. By using known genetic relationships between Brachypodium lines, multiple sets of nearly identical accession families were selected for phenotypic studies and DNA methylome profiling to investigate the dual role of (epi)genetics under simulated natural seasonal climate conditions. Despite reduced genetic diversity, appreciable phenotypic variation was still observable in the measured traits (height, leaf width and length, tiller count, flowering time, ear count) between as well as within the inbred accessions. However, with reduced genetic diversity there was diminished variation in DNA methylation within families. Mixed-effects linear modeling revealed large genetic differences between families and a minor contribution of DNA methylation variation on phenotypic variation in select traits. Taken together, this analysis suggests a limited but significant contribution of DNA methylation toward heritable phenotypic variation relative to genetic differences.
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spelling pubmed-72020212020-05-09 Extending the Genotype in Brachypodium by Including DNA Methylation Reveals a Joint Contribution with Genetics on Adaptive Traits Eichten, Steven R. Srivastava, Akanksha Reddiex, Adam J. Ganguly, Diep R. Heussler, Alison Streich, Jared C. Wilson, Pip B. Borevitz, Justin O. G3 (Bethesda) Investigations Epigenomic changes have been considered a potential missing link underlying phenotypic variation in quantitative traits but is potentially confounded with the underlying DNA sequence variation. Although the concept of epigenetic inheritance has been discussed in depth, there have been few studies attempting to directly dissect the amount of epigenomic variation within inbred natural populations while also accounting for genetic diversity. By using known genetic relationships between Brachypodium lines, multiple sets of nearly identical accession families were selected for phenotypic studies and DNA methylome profiling to investigate the dual role of (epi)genetics under simulated natural seasonal climate conditions. Despite reduced genetic diversity, appreciable phenotypic variation was still observable in the measured traits (height, leaf width and length, tiller count, flowering time, ear count) between as well as within the inbred accessions. However, with reduced genetic diversity there was diminished variation in DNA methylation within families. Mixed-effects linear modeling revealed large genetic differences between families and a minor contribution of DNA methylation variation on phenotypic variation in select traits. Taken together, this analysis suggests a limited but significant contribution of DNA methylation toward heritable phenotypic variation relative to genetic differences. Genetics Society of America 2020-03-04 /pmc/articles/PMC7202021/ /pubmed/32132166 http://dx.doi.org/10.1534/g3.120.401189 Text en Copyright © 2020 Eichten et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International 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 Investigations
Eichten, Steven R.
Srivastava, Akanksha
Reddiex, Adam J.
Ganguly, Diep R.
Heussler, Alison
Streich, Jared C.
Wilson, Pip B.
Borevitz, Justin O.
Extending the Genotype in Brachypodium by Including DNA Methylation Reveals a Joint Contribution with Genetics on Adaptive Traits
title Extending the Genotype in Brachypodium by Including DNA Methylation Reveals a Joint Contribution with Genetics on Adaptive Traits
title_full Extending the Genotype in Brachypodium by Including DNA Methylation Reveals a Joint Contribution with Genetics on Adaptive Traits
title_fullStr Extending the Genotype in Brachypodium by Including DNA Methylation Reveals a Joint Contribution with Genetics on Adaptive Traits
title_full_unstemmed Extending the Genotype in Brachypodium by Including DNA Methylation Reveals a Joint Contribution with Genetics on Adaptive Traits
title_short Extending the Genotype in Brachypodium by Including DNA Methylation Reveals a Joint Contribution with Genetics on Adaptive Traits
title_sort extending the genotype in brachypodium by including dna methylation reveals a joint contribution with genetics on adaptive traits
topic Investigations
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7202021/
https://www.ncbi.nlm.nih.gov/pubmed/32132166
http://dx.doi.org/10.1534/g3.120.401189
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