Abstract

BackgroundGenetic variance that is not captured by single nucleotide polymorphisms (SNPs) is due to imperfect linkage disequilibrium (LD) between SNPs and quantitative trait loci (QTLs), and the extent of LD between SNPs and QTLs depends on different minor allele frequencies (MAF) between them. To evaluate the impact of MAF of QTLs on genomic evaluation, we performed a simulation study using real cattle genotype data.MethodsIn total, 1368 Japanese Black cattle and 592,034 SNPs (Illumina BovineHD BeadChip) were used. We simulated phenotypes using real genotypes under different scenarios, varying the MAF categories, QTL heritability, number of QTLs, and distribution of QTL effect. After generating true breeding values and phenotypes, QTL heritability was estimated and the prediction accuracy of genomic estimated breeding value (GEBV) was assessed under different SNP densities, prediction models, and population size by a reference-test validation design.ResultsThe extent of LD between SNPs and QTLs in this population was higher in the QTLs with high MAF than in those with low MAF. The effect of MAF of QTLs depended on the genetic architecture, evaluation strategy, and population size in genomic evaluation. In genetic architecture, genomic evaluation was affected by the MAF of QTLs combined with the QTL heritability and the distribution of QTL effect. The number of QTL was not affected on genomic evaluation if the number of QTL was more than 50. In the evaluation strategy, we showed that different SNP densities and prediction models affect the heritability estimation and genomic prediction and that this depends on the MAF of QTLs. In addition, accurate QTL heritability and GEBV were obtained using denser SNP information and the prediction model accounted for the SNPs with low and high MAFs. In population size, a large sample size is needed to increase the accuracy of GEBV.ConclusionThe MAF of QTL had an impact on heritability estimation and prediction accuracy. Most genetic variance can be captured using denser SNPs and the prediction model accounted for MAF, but a large sample size is needed to increase the accuracy of GEBV under all QTL MAF categories.Electronic supplementary materialThe online version of this article (doi:10.1186/s12863-015-0287-8) contains supplementary material, which is available to authorized users.

Highlights

  • Genetic variance that is not captured by single nucleotide polymorphisms (SNPs) is due to imperfect linkage disequilibrium (LD) between SNPs and quantitative trait loci (QTLs), and the extent of LD between SNPs and Quantitative trait locus (QTL) depends on different minor allele frequencies (MAF) between them

  • Whole genome sequence (WGS) data are becoming increasingly available for cattle, and whole genome sequence (WGS) data are expected to yield a better understanding of complex traits, which can capture all of the genetic variance and predict an accurate genomic estimated breeding value (GEBV), by accounting for all the variants including quantitative trait loci (QTLs) [3, 4]

  • The mean values of r2 for all, high, and low minor allele frequency (MAF) were 0.294, 0.360, and 0.184, respectively. This shows that the extent of LD between SNPs and QTLs is higher in the QTLs with high MAF than that in those with low MAF

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Summary

Introduction

Genetic variance that is not captured by single nucleotide polymorphisms (SNPs) is due to imperfect linkage disequilibrium (LD) between SNPs and quantitative trait loci (QTLs), and the extent of LD between SNPs and QTLs depends on different minor allele frequencies (MAF) between them. QTLs may have a lower MAF than SNPs on low-density SNP arrays, because these are designed to work in several different breeds In this case, the genetic variation explained by SNPs will be lower than that due to low LD between SNPs and QTLs with low MAF. The extent of LD between SNPs and QTLs in Japanese Black cattle may differ from that in other cattle breeds, and it is necessary to evaluate the impact of MAF of QTLs on the genomic evaluation in this target population

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