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Prediction of Subgenome Additive and Interaction Effects in Allohexaploid Wheat

Whole genome duplications have played an important role in the evolution of angiosperms. These events often occur through hybridization between closely related species, resulting in an allopolyploid with multiple subgenomes. With the availability of affordable genotyping and a reference genome to lo...

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Autores principales: Santantonio, Nicholas, Jannink, Jean-Luc, Sorrells, Mark
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Genetics Society of America 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6404612/
https://www.ncbi.nlm.nih.gov/pubmed/30455185
http://dx.doi.org/10.1534/g3.118.200613
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author Santantonio, Nicholas
Jannink, Jean-Luc
Sorrells, Mark
author_facet Santantonio, Nicholas
Jannink, Jean-Luc
Sorrells, Mark
author_sort Santantonio, Nicholas
collection PubMed
description Whole genome duplications have played an important role in the evolution of angiosperms. These events often occur through hybridization between closely related species, resulting in an allopolyploid with multiple subgenomes. With the availability of affordable genotyping and a reference genome to locate markers, breeders of allopolyploids now have the opportunity to manipulate subgenomes independently. This also presents a unique opportunity to investigate epistatic interactions between homeologous orthologs across subgenomes. We present a statistical framework for partitioning genetic variance to the subgenomes of an allopolyploid, predicting breeding values for each subgenome, and determining the importance of inter-genomic epistasis. We demonstrate using an allohexaploid wheat breeding population evaluated in Ithaca, NY and an important wheat dataset from CIMMYT previously shown to demonstrate non-additive genetic variance. Subgenome covariance matrices were constructed and used to calculate subgenome interaction covariance matrices for variance component estimation and genomic prediction. We propose a method to extract population structure from all subgenomes at once before covariances are calculated to reduce collinearity between subgenome estimates. Variance parameter estimation was shown to be reliable for additive subgenome effects, but was less reliable for subgenome interaction components. Predictive ability was equivalent to current genomic prediction methods. Including only inter-genomic interactions resulted in the same increase in accuracy as modeling all pairwise marker interactions. Thus, we provide a new tool for breeders of allopolyploid crops to characterize the genetic architecture of existing populations, determine breeding goals, and develop new strategies for selection of additive effects and fixation of inter-genomic epistasis.
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spelling pubmed-64046122019-03-11 Prediction of Subgenome Additive and Interaction Effects in Allohexaploid Wheat Santantonio, Nicholas Jannink, Jean-Luc Sorrells, Mark G3 (Bethesda) Genomic Prediction Whole genome duplications have played an important role in the evolution of angiosperms. These events often occur through hybridization between closely related species, resulting in an allopolyploid with multiple subgenomes. With the availability of affordable genotyping and a reference genome to locate markers, breeders of allopolyploids now have the opportunity to manipulate subgenomes independently. This also presents a unique opportunity to investigate epistatic interactions between homeologous orthologs across subgenomes. We present a statistical framework for partitioning genetic variance to the subgenomes of an allopolyploid, predicting breeding values for each subgenome, and determining the importance of inter-genomic epistasis. We demonstrate using an allohexaploid wheat breeding population evaluated in Ithaca, NY and an important wheat dataset from CIMMYT previously shown to demonstrate non-additive genetic variance. Subgenome covariance matrices were constructed and used to calculate subgenome interaction covariance matrices for variance component estimation and genomic prediction. We propose a method to extract population structure from all subgenomes at once before covariances are calculated to reduce collinearity between subgenome estimates. Variance parameter estimation was shown to be reliable for additive subgenome effects, but was less reliable for subgenome interaction components. Predictive ability was equivalent to current genomic prediction methods. Including only inter-genomic interactions resulted in the same increase in accuracy as modeling all pairwise marker interactions. Thus, we provide a new tool for breeders of allopolyploid crops to characterize the genetic architecture of existing populations, determine breeding goals, and develop new strategies for selection of additive effects and fixation of inter-genomic epistasis. Genetics Society of America 2018-11-19 /pmc/articles/PMC6404612/ /pubmed/30455185 http://dx.doi.org/10.1534/g3.118.200613 Text en Copyright © 2019 Santantonio 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 Genomic Prediction
Santantonio, Nicholas
Jannink, Jean-Luc
Sorrells, Mark
Prediction of Subgenome Additive and Interaction Effects in Allohexaploid Wheat
title Prediction of Subgenome Additive and Interaction Effects in Allohexaploid Wheat
title_full Prediction of Subgenome Additive and Interaction Effects in Allohexaploid Wheat
title_fullStr Prediction of Subgenome Additive and Interaction Effects in Allohexaploid Wheat
title_full_unstemmed Prediction of Subgenome Additive and Interaction Effects in Allohexaploid Wheat
title_short Prediction of Subgenome Additive and Interaction Effects in Allohexaploid Wheat
title_sort prediction of subgenome additive and interaction effects in allohexaploid wheat
topic Genomic Prediction
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6404612/
https://www.ncbi.nlm.nih.gov/pubmed/30455185
http://dx.doi.org/10.1534/g3.118.200613
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