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Multigenerational prediction of genetic values using genome-enabled prediction.

ABSTRACT: The identification of elite individuals is a critical component of most breeding programs. However, the achievement of this goal is limited by the high cost of phenotyping and experimental research. A significant benefit of genomic selection (GS) to plant breeding is the identification of elite individuals without the need for phenotyping. This study aimed to propose different calibration strategies using combinations between generations from different genetic backgrounds to improve the reliability of GS and to investigate the effects of LD in different types of mating systems: outcrossing (An) self-pollination (Sn) and hybridization (Hn). For this purpose, we simulated a genome with 10 linkage groups. In each group, two QTL were simulated. Subsequently, an F2 population was created, followed by four generations of inbreeding (S1 to S4, H1 to H 4, A1, to A4,). Quantitative traits were simulated in three scenarios considering three degrees of dominance (d/a = 0, 0.5 and 1) and two broad sense heritabilities (h2 = 0.30 and 0.70), totaling six genetic architectures. To evaluate prediction reliability, a model (RR-BLUP) was trained in one generation and used to predict the following generations of mating systems. For example, the marker effects estimated in the F2 population were used to estimate the expected genomic breeding value (GEBV) in populations S1 through A4. The squared correlation between the GEBV and the true genetic value were used to measure the reliability of the predictions. Independently of the population used to estimate the marker effect, reliability showed the lowest values in the scenario where d = 1. For any scenario, the use of the multigenerational prediction methodology improved the reliability of GS.

SUBMITTER: Sant' Anna IC

PROVIDER: S-EPMC6336252 | biostudies-literature | 2019

REPOSITORIES: biostudies-literature

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Multigenerational prediction of genetic values using genome-enabled prediction.

Sant' Anna Isabela de Castro IC Cabral Ferreira Ricardo Augusto Diniz RAD Nascimento Moysés M Silva Gabi Nunes GN Carneiro Vinicius Quintão VQ Cruz Cosme Damião CD Oliveira Marciane Silva MS Chagas Francyse Edith FE

PloS one 20190117 1

The identification of elite individuals is a critical component of most breeding programs. However, the achievement of this goal is limited by the high cost of phenotyping and experimental research. A significant benefit of genomic selection (GS) to plant breeding is the identification of elite individuals without the need for phenotyping. This study aimed to propose different calibration strategies using combinations between generations from different genetic backgrounds to improve the reliabil ...[more]

PMID: 30653561

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Project description:BackgroundMolecular marker information is a common source to draw inferences about the relationship between genetic and phenotypic variation. Genetic effects are often modelled as additively acting marker allele effects. The true mode of biological action can, of course, be different from this plain assumption. One possibility to better understand the genetic architecture of complex traits is to include intra-locus (dominance) and inter-locus (epistasis) interaction of alleles as well as the additive genetic effects when fitting a model to a trait. Several Bayesian MCMC approaches exist for the genome-wide estimation of genetic effects with high accuracy of genetic value prediction. Including pairwise interaction for thousands of loci would probably go beyond the scope of such a sampling algorithm because then millions of effects are to be estimated simultaneously leading to months of computation time. Alternative solving strategies are required when epistasis is studied.MethodsWe extended a fast Bayesian method (fBayesB), which was previously proposed for a purely additive model, to include non-additive effects. The fBayesB approach was used to estimate genetic effects on the basis of simulated datasets. Different scenarios were simulated to study the loss of accuracy of prediction, if epistatic effects were not simulated but modelled and vice versa.ResultsIf 23 QTL were simulated to cause additive and dominance effects, both fBayesB and a conventional MCMC sampler BayesB yielded similar results in terms of accuracy of genetic value prediction and bias of variance component estimation based on a model including additive and dominance effects. Applying fBayesB to data with epistasis, accuracy could be improved by 5% when all pairwise interactions were modelled as well. The accuracy decreased more than 20% if genetic variation was spread over 230 QTL. In this scenario, accuracy based on modelling only additive and dominance effects was generally superior to that of the complex model including epistatic effects.ConclusionsThis simulation study showed that the fBayesB approach is convenient for genetic value prediction. Jointly estimating additive and non-additive effects (especially dominance) has reasonable impact on the accuracy of prediction and the proportion of genetic variation assigned to the additive genetic source.

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Multigenerational prediction of genetic values using genome-enabled prediction.

Publications

Multigenerational prediction of genetic values using genome-enabled prediction.

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