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Genomic prediction of the recombination rate variation in barley – A route to highly recombinogenic genotypes

Meiotic recombination is not only fundamental to the adaptation of sexually reproducing eukaryotes in nature but increased recombination rates facilitate the combination of favourable alleles into a single haplotype in breeding programmes. The main objectives of this study were to (i) assess the ext...

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Autores principales: Casale, Federico, Van Inghelandt, Delphine, Weisweiler, Marius, Li, Jinquan, Stich, Benjamin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8989500/
https://www.ncbi.nlm.nih.gov/pubmed/34783155
http://dx.doi.org/10.1111/pbi.13746
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author Casale, Federico
Van Inghelandt, Delphine
Weisweiler, Marius
Li, Jinquan
Stich, Benjamin
author_facet Casale, Federico
Van Inghelandt, Delphine
Weisweiler, Marius
Li, Jinquan
Stich, Benjamin
author_sort Casale, Federico
collection PubMed
description Meiotic recombination is not only fundamental to the adaptation of sexually reproducing eukaryotes in nature but increased recombination rates facilitate the combination of favourable alleles into a single haplotype in breeding programmes. The main objectives of this study were to (i) assess the extent and distribution of the recombination rate variation in cultivated barley (Hordeum vulgare L.), (ii) quantify the importance of the general and specific recombination effects, and (iii) evaluate a genomic selection approach’s ability to predict the recombination rate variation. Genetic maps were created for the 45 segregating populations that were derived from crosses among 23 spring barley inbreds with origins across the world. The genome‐wide recombination rate among populations ranged from 0.31 to 0.73 cM/Mbp. The crossing design used in this study allowed to separate the general recombination effects (GRE) of individual parental inbreds from the specific recombination effects (SRE) caused by the combinations of parental inbreds. The variance of the genome‐wide GRE was found to be about eight times the variance of the SRE. This finding indicated that parental inbreds differ in the efficiency of their recombination machinery. The ability to predict the chromosome or genome‐wide recombination rate of an inbred ranged from 0.80 to 0.85. These results suggest that a reliable screening of large genetic materials for their potential to cause a high extent of genetic recombination in their progeny is possible, allowing to systematically manipulate the recombination rate using natural variation.
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spelling pubmed-89895002022-04-13 Genomic prediction of the recombination rate variation in barley – A route to highly recombinogenic genotypes Casale, Federico Van Inghelandt, Delphine Weisweiler, Marius Li, Jinquan Stich, Benjamin Plant Biotechnol J Research Articles Meiotic recombination is not only fundamental to the adaptation of sexually reproducing eukaryotes in nature but increased recombination rates facilitate the combination of favourable alleles into a single haplotype in breeding programmes. The main objectives of this study were to (i) assess the extent and distribution of the recombination rate variation in cultivated barley (Hordeum vulgare L.), (ii) quantify the importance of the general and specific recombination effects, and (iii) evaluate a genomic selection approach’s ability to predict the recombination rate variation. Genetic maps were created for the 45 segregating populations that were derived from crosses among 23 spring barley inbreds with origins across the world. The genome‐wide recombination rate among populations ranged from 0.31 to 0.73 cM/Mbp. The crossing design used in this study allowed to separate the general recombination effects (GRE) of individual parental inbreds from the specific recombination effects (SRE) caused by the combinations of parental inbreds. The variance of the genome‐wide GRE was found to be about eight times the variance of the SRE. This finding indicated that parental inbreds differ in the efficiency of their recombination machinery. The ability to predict the chromosome or genome‐wide recombination rate of an inbred ranged from 0.80 to 0.85. These results suggest that a reliable screening of large genetic materials for their potential to cause a high extent of genetic recombination in their progeny is possible, allowing to systematically manipulate the recombination rate using natural variation. John Wiley and Sons Inc. 2021-12-11 2022-04 /pmc/articles/PMC8989500/ /pubmed/34783155 http://dx.doi.org/10.1111/pbi.13746 Text en © 2021 The Authors. Plant Biotechnology Journal published by Society for Experimental Biology and The Association of Applied Biologists and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Casale, Federico
Van Inghelandt, Delphine
Weisweiler, Marius
Li, Jinquan
Stich, Benjamin
Genomic prediction of the recombination rate variation in barley – A route to highly recombinogenic genotypes
title Genomic prediction of the recombination rate variation in barley – A route to highly recombinogenic genotypes
title_full Genomic prediction of the recombination rate variation in barley – A route to highly recombinogenic genotypes
title_fullStr Genomic prediction of the recombination rate variation in barley – A route to highly recombinogenic genotypes
title_full_unstemmed Genomic prediction of the recombination rate variation in barley – A route to highly recombinogenic genotypes
title_short Genomic prediction of the recombination rate variation in barley – A route to highly recombinogenic genotypes
title_sort genomic prediction of the recombination rate variation in barley – a route to highly recombinogenic genotypes
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8989500/
https://www.ncbi.nlm.nih.gov/pubmed/34783155
http://dx.doi.org/10.1111/pbi.13746
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