Abstract

BackgroundIn crossbreeding schemes, within-line selection of purebreds is performed mainly to improve the performance of crossbred descendants under field conditions. The genetic correlation between purebred and crossbred performance is an important parameter to be assessed because purebred performance can be a poor predictor of the performance of crossbred offspring. With the availability of high-density markers, the feasibility of using crossbred information to evaluate purebred candidates can be reassessed. This study implements and applies a single-step terminal-cross model (GEN) to real data to estimate the genetic parameters of several production and quality traits in pigs.MethodsPiétrain sires were mated with Piétrain and Large White dams to produce purebred and crossbred male half-sib piglets; growth rate, feed conversion ratio, lean meat, pH of longissimus dorsi muscle, drip loss and intramuscular fat content were recorded on all half-sibs. Animals were genotyped using the Illumina Porcine SNP60 BeadChip. The genetic correlation between purebred and crossbred performance was estimated separately for each trait. Purebred animals were evaluated using an animal model, whereas the additive genetic effect of a crossbred individual was decomposed into the additive effects of the sire and dam and a Mendelian sampling effect that was confounded with the residual effect. Genotypes of the Piétrain animals were integrated in the genetic evaluation by using a single-step procedure. As benchmarks, we used a model that was identical to GEN but only accounted for pedigree information (PED) and also two univariate single-step models (GEN_UNI) that took either purebred or crossbred performance into account.ResultsGenetic correlations between purebred and crossbred performance were high and positive for all traits (>0.69). Accuracies of estimated breeding values of genotyped sires and purebred offspring that were obtained with the GEN model outperformed both those obtained with the PED and the GEN_UNI models. The use of genomic information increased the predictive ability of the GEN model, but it did not substantially outperform the GEN_UNI models.ConclusionsWe present a single-step terminal-cross model that integrates genomic information of purebred and crossbred performance by using available software. It improves the theoretical accuracy of genetic evaluations in breeding programs that are based on crossbreeding.

Highlights

  • In crossbreeding schemes, within-line selection of purebreds is performed mainly to improve the per‐ formance of crossbred descendants under field conditions

  • We developed and tested on a real pig dataset a single-step terminal-cross model to estimate the genetic parameters of several production and quality traits

  • We proposed and applied on real data a single-step terminal-cross model that accounts for genomic information on PB individuals and uses CB performance to estimate genetic parameters of several production and quality traits in pigs

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Summary

Introduction

Within-line selection of purebreds is performed mainly to improve the per‐ formance of crossbred descendants under field conditions. The theory on which selection for CB performance is based was largely developed and discussed many years ago [3], but until now, the use of CB information to evaluate the PB parental lines has not resulted in a clear advantage for within-line PB selection and has not been widely implemented in practice. This is primarily due to practical difficulties in tracing CB pedigrees and performances back to their PB parents. The use of genomic information can improve response to selection by increasing the accuracy of genetic evaluations, increasing the number of candidates for selection, performing genetic evaluations at an earlier age than with traditional approaches, lowering the rate of inbreeding, avoiding the need for pedigree information to connect PB and CB individuals (depending on the method used), and accommodating non-additive genetic effects that can impact CB performance (i.e. dominance and heterosis) [4, 5]

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