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Optimizing genomic selection for blight resistance in American chestnut backcross populations: A trade‐off with American chestnut ancestry implies resistance is polygenic

American chestnut was once a foundation species of eastern North American forests, but was rendered functionally extinct in the early 20th century by an exotic fungal blight (Cryphonectria parasitica). Over the past 30 years, the American Chestnut Foundation (TACF) has pursued backcross breeding to...

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Autores principales: Westbrook, Jared W., Zhang, Qian, Mandal, Mihir K., Jenkins, Eric V., Barth, Laura E., Jenkins, Jerry W., Grimwood, Jane, Schmutz, Jeremy, Holliday, Jason A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6935594/
https://www.ncbi.nlm.nih.gov/pubmed/31892942
http://dx.doi.org/10.1111/eva.12886
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author Westbrook, Jared W.
Zhang, Qian
Mandal, Mihir K.
Jenkins, Eric V.
Barth, Laura E.
Jenkins, Jerry W.
Grimwood, Jane
Schmutz, Jeremy
Holliday, Jason A.
author_facet Westbrook, Jared W.
Zhang, Qian
Mandal, Mihir K.
Jenkins, Eric V.
Barth, Laura E.
Jenkins, Jerry W.
Grimwood, Jane
Schmutz, Jeremy
Holliday, Jason A.
author_sort Westbrook, Jared W.
collection PubMed
description American chestnut was once a foundation species of eastern North American forests, but was rendered functionally extinct in the early 20th century by an exotic fungal blight (Cryphonectria parasitica). Over the past 30 years, the American Chestnut Foundation (TACF) has pursued backcross breeding to generate hybrids that combine the timber‐type form of American chestnut with the blight resistance of Chinese chestnut based on a hypothesis of major gene resistance. To accelerate selection within two backcross populations that descended from two Chinese chestnuts, we developed genomic prediction models for five presence/absence blight phenotypes of 1,230 BC(3)F(2) selection candidates and average canker severity of their BC(3)F(3) progeny. We also genotyped pure Chinese and American chestnut reference panels to estimate the proportion of BC(3)F(2) genomes inherited from parent species. We found that genomic prediction from a method that assumes an infinitesimal model of inheritance (HBLUP) has similar accuracy to a method that tends to perform well for traits controlled by major genes (Bayes C). Furthermore, the proportion of BC(3)F(2) trees' genomes inherited from American chestnut was negatively correlated with the blight resistance of these trees and their progeny. On average, selected BC(3)F(2) trees inherited 83% of their genome from American chestnut and have blight resistance that is intermediate between F(1) hybrids and American chestnut. Results suggest polygenic inheritance of blight resistance. The blight resistance of restoration populations will be enhanced through recurrent selection, by advancing additional sources of resistance through fewer backcross generations, and by potentially by breeding with transgenic blight‐tolerant trees.
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spelling pubmed-69355942019-12-31 Optimizing genomic selection for blight resistance in American chestnut backcross populations: A trade‐off with American chestnut ancestry implies resistance is polygenic Westbrook, Jared W. Zhang, Qian Mandal, Mihir K. Jenkins, Eric V. Barth, Laura E. Jenkins, Jerry W. Grimwood, Jane Schmutz, Jeremy Holliday, Jason A. Evol Appl Special Issue Original Articles American chestnut was once a foundation species of eastern North American forests, but was rendered functionally extinct in the early 20th century by an exotic fungal blight (Cryphonectria parasitica). Over the past 30 years, the American Chestnut Foundation (TACF) has pursued backcross breeding to generate hybrids that combine the timber‐type form of American chestnut with the blight resistance of Chinese chestnut based on a hypothesis of major gene resistance. To accelerate selection within two backcross populations that descended from two Chinese chestnuts, we developed genomic prediction models for five presence/absence blight phenotypes of 1,230 BC(3)F(2) selection candidates and average canker severity of their BC(3)F(3) progeny. We also genotyped pure Chinese and American chestnut reference panels to estimate the proportion of BC(3)F(2) genomes inherited from parent species. We found that genomic prediction from a method that assumes an infinitesimal model of inheritance (HBLUP) has similar accuracy to a method that tends to perform well for traits controlled by major genes (Bayes C). Furthermore, the proportion of BC(3)F(2) trees' genomes inherited from American chestnut was negatively correlated with the blight resistance of these trees and their progeny. On average, selected BC(3)F(2) trees inherited 83% of their genome from American chestnut and have blight resistance that is intermediate between F(1) hybrids and American chestnut. Results suggest polygenic inheritance of blight resistance. The blight resistance of restoration populations will be enhanced through recurrent selection, by advancing additional sources of resistance through fewer backcross generations, and by potentially by breeding with transgenic blight‐tolerant trees. John Wiley and Sons Inc. 2019-12-29 /pmc/articles/PMC6935594/ /pubmed/31892942 http://dx.doi.org/10.1111/eva.12886 Text en © 2019 The Authors. Evolutionary Applications published by John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Special Issue Original Articles
Westbrook, Jared W.
Zhang, Qian
Mandal, Mihir K.
Jenkins, Eric V.
Barth, Laura E.
Jenkins, Jerry W.
Grimwood, Jane
Schmutz, Jeremy
Holliday, Jason A.
Optimizing genomic selection for blight resistance in American chestnut backcross populations: A trade‐off with American chestnut ancestry implies resistance is polygenic
title Optimizing genomic selection for blight resistance in American chestnut backcross populations: A trade‐off with American chestnut ancestry implies resistance is polygenic
title_full Optimizing genomic selection for blight resistance in American chestnut backcross populations: A trade‐off with American chestnut ancestry implies resistance is polygenic
title_fullStr Optimizing genomic selection for blight resistance in American chestnut backcross populations: A trade‐off with American chestnut ancestry implies resistance is polygenic
title_full_unstemmed Optimizing genomic selection for blight resistance in American chestnut backcross populations: A trade‐off with American chestnut ancestry implies resistance is polygenic
title_short Optimizing genomic selection for blight resistance in American chestnut backcross populations: A trade‐off with American chestnut ancestry implies resistance is polygenic
title_sort optimizing genomic selection for blight resistance in american chestnut backcross populations: a trade‐off with american chestnut ancestry implies resistance is polygenic
topic Special Issue Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6935594/
https://www.ncbi.nlm.nih.gov/pubmed/31892942
http://dx.doi.org/10.1111/eva.12886
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