Abstract

BackgroundDifferences in linkage disequilibrium and in allele substitution effects of QTL (quantitative trait loci) may hinder genomic prediction across populations. Our objective was to develop a deterministic formula to estimate the accuracy of across-population genomic prediction, for which reference individuals and selection candidates are from different populations, and to investigate the impact of differences in allele substitution effects across populations and of the number of QTL underlying a trait on the accuracy.MethodsA deterministic formula to estimate the accuracy of across-population genomic prediction was derived based on selection index theory. Moreover, accuracies were deterministically predicted using a formula based on population parameters and empirically calculated using simulated phenotypes and a GBLUP (genomic best linear unbiased prediction) model. Phenotypes of 1033 Holstein-Friesian, 105 Groninger White Headed and 147 Meuse-Rhine-Yssel cows were simulated by sampling 3000, 300, 30 or 3 QTL from the available high-density SNP (single nucleotide polymorphism) information of three chromosomes, assuming a correlation of 1.0, 0.8, 0.6, 0.4, or 0.2 between allele substitution effects across breeds. The simulated heritability was set to 0.95 to resemble the heritability of deregressed proofs of bulls.ResultsAccuracies estimated with the deterministic formula based on selection index theory were similar to empirical accuracies for all scenarios, while accuracies predicted with the formula based on population parameters overestimated empirical accuracies by ~25 to 30%. When the between-breed genetic correlation differed from 1, i.e. allele substitution effects differed across breeds, empirical and deterministic accuracies decreased in proportion to the genetic correlation. Using a multi-trait model, it was possible to accurately estimate the genetic correlation between the breeds based on phenotypes and high-density genotypes. The number of QTL underlying the simulated trait did not affect the accuracy.ConclusionsThe deterministic formula based on selection index theory estimated the accuracy of across-population genomic predictions well. The deterministic formula using population parameters overestimated the across-population genomic accuracy, but may still be useful because of its simplicity. Both formulas could accommodate for genetic correlations between populations lower than 1. The number of QTL underlying a trait did not affect the accuracy of across-population genomic prediction using a GBLUP method.

Highlights

  • Differences in linkage disequilibrium and in allele substitution effects of quantitative trait loci (QTL) may hinder genomic prediction across populations

  • In cases where allele substitution effects were equal across breeds, differences in accuracy between single- and across-breed genomic predictions were due to differences in allele frequencies, relationships and linkage disequilibrium (LD) pattern across breeds

  • The deterministic formula based on selection index theory can take those heterogeneous variances into account as well, in contrast to the application of the formula based on populations parameters described here

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Summary

Introduction

Differences in linkage disequilibrium and in allele substitution effects of QTL (quantitative trait loci) may hinder genomic prediction across populations. Our objective was to develop a deterministic formula to estimate the accuracy of across-population genomic prediction, for which reference individuals and selection candidates are from different populations, and to investigate the impact of differences in allele substitution effects across populations and of the number of QTL underlying a trait on the accuracy. The accuracy of predicting breeding values for selection candidates within one population is influenced by the level of linkage disequilibrium (LD) between markers, i.e. single-nucleotide polymorphisms (SNPs) and quantitative trait loci (QTL) that influence the trait, and by the level of family relationships [1,2,3,4]. The concept of combining individuals of different breeds in cattle is essentially similar to combining individuals from different lines in other animal and plant species, e.g. [4,12,13] or from different subpopulations in humans, e.g. [3,6] because close family relationships are absent and the extent of LD is limited across breeds, lines, and subpopulations

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