Abstract

BackgroundGenomic selection has become an important tool in the genetic improvement of animals and plants. The objective of this study was to investigate the impacts of breeding value estimation method, reference population structure, and trait genetic architecture, on long-term response to genomic selection without updating marker effects.MethodsThree methods were used to estimate genomic breeding values: a BLUP method with relationships estimated from genome-wide markers (GBLUP), a Bayesian method, and a partial least squares regression method (PLSR). A shallow (individuals from one generation) or deep reference population (individuals from five generations) was used with each method. The effects of the different selection approaches were compared under four different genetic architectures for the trait under selection. Selection was based on one of the three genomic breeding values, on pedigree BLUP breeding values, or performed at random. Selection continued for ten generations.ResultsDifferences in long-term selection response were small. For a genetic architecture with a very small number of three to four quantitative trait loci (QTL), the Bayesian method achieved a response that was 0.05 to 0.1 genetic standard deviation higher than other methods in generation 10. For genetic architectures with approximately 30 to 300 QTL, PLSR (shallow reference) or GBLUP (deep reference) had an average advantage of 0.2 genetic standard deviation over the Bayesian method in generation 10. GBLUP resulted in 0.6% and 0.9% less inbreeding than PLSR and BM and on average a one third smaller reduction of genetic variance. Responses in early generations were greater with the shallow reference population while long-term response was not affected by reference population structure.ConclusionsThe ranking of estimation methods was different with than without selection. Under selection, applying GBLUP led to lower inbreeding and a smaller reduction of genetic variance while a similar response to selection was achieved. The reference population structure had a limited effect on long-term accuracy and response. Use of a shallow reference population, most closely related to the selection candidates, gave early benefits while in later generations, when marker effects were not updated, the estimation of marker effects based on a deeper reference population did not pay off.

Highlights

  • Genomic selection has become an important tool in the genetic improvement of animals and plants

  • In this study, response to selection was determined over ten generations with different selection approaches that combined one of the following estimation methods Bayesian method (BM), BLUP, genomic BLUP (GBLUP) or partial least square regression (PLSR) with a deep or shallow reference population structure

  • Under selection, applying GBLUP leads to lower inbreeding and a smaller reduction of genetic variance especially in comparison to PLSR and to BM, while a similar genetic improvement is achieved with these estimation methods for traits that have a moderate to large number of quantitative trait loci (QTL)

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Summary

Introduction

Genomic selection has become an important tool in the genetic improvement of animals and plants. The objective of this study was to investigate the impacts of breeding value estimation method, reference population structure, and trait genetic architecture, on long-term response to genomic selection without updating marker effects. More persistent accuracies of MEBV are expected when the average distance between markers and QTL decreases, as this leads to lower recombination rates [18]. The structure of the reference population is expected to have an effect on the persistence of accuracies because it affects how well the genetic variance of QTL can be assigned to markers near the QTL as opposed to markers that are more distant. Selecting animals for the reference population across more generations will reduce the average relationship within the reference population and is expected to lead to more persistent accuracies of MEBV. In populations under selection, LD is expected to change more rapidly compared to unselected populations, with the result that accuracies of the MEBV decrease faster under selection [5,11]

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