Abstract

BackgroundBody weight (BW) is an important trait for meat production in sheep. Although over the past few years, numerous quantitative trait loci (QTL) have been detected for production traits in cattle, few QTL studies have been reported for sheep, with even fewer on meat production traits. Our objective was to perform a genome-wide association study (GWAS) with the medium-density Illumina Ovine SNP50 BeadChip to identify genomic regions and corresponding haplotypes associated with BW in Australian Merino sheep.MethodsA total of 1781 Australian Merino sheep were genotyped using the medium-density Illumina Ovine SNP50 BeadChip. Among the 53 862 single nucleotide polymorphisms (SNPs) on this array, 48 640 were used to perform a GWAS using a linear mixed model approach. Genotypes were phased with hsphase; to estimate SNP haplotype effects, linkage disequilibrium blocks were identified in the detected QTL region.ResultsThirty-nine SNPs were associated with BW at a Bonferroni-corrected genome-wide significance threshold of 1 %. One region on sheep (Ovis aries) chromosome 6 (OAR6) between 36.15 and 38.56 Mb, included 13 significant SNPs that were associated with BW; the most significant SNP was OAR6_41936490.1 (P = 2.37 × 10−16) at 37.69 Mb with an allele substitution effect of 2.12 kg, which corresponds to 0.248 phenotypic standard deviations for BW. The region that surrounds this association signal on OAR6 contains three genes: leucine aminopeptidase 3 (LAP3), which is involved in the processing of the oxytocin precursor; NCAPG non-SMC condensin I complex, subunit G (NCAPG), which is associated with foetal growth and carcass size in cattle; and ligand dependent nuclear receptor corepressor-like (LCORL), which is associated with height in humans and cattle.ConclusionsThe GWAS analysis detected 39 SNPs associated with BW in sheep and a major QTL region was identified on OAR6. In several other mammalian species, regions that are syntenic with this region have been found to be associated with body size traits, which may reflect that the underlying biological mechanisms share a common ancestry. These findings should facilitate the discovery of causative variants for BW and contribute to marker-assisted selection.Electronic supplementary materialThe online version of this article (doi:10.1186/s12711-015-0142-4) contains supplementary material, which is available to authorized users.

Highlights

  • Body weight (BW) is an important trait for meat production in sheep

  • Our aims were (1) to perform a genome-wide association study (GWAS) to detect significant single nucleotide polymorphisms (SNPs) that are associated with BW in sheep by using data from 1781 Australian Merino sheep genotyped with the Illumina Ovine SNP50 BeadChip and (2)

  • Based on the Ovis aries reference genome assembly (Oar_v3.1), the region between 36.15 and 38.56 Mb on OAR6 contains 14 genes. These include NCAPG nonSMC condensin I complex, subunit G (NCAPG), which is associated with foetal growth and carcass size in cattle [33], and ligand dependent nuclear receptor corepressor-like (LCORL), which is associated with height in humans and cattle [14, 15] (Table 2 and Fig. 4)

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Summary

Introduction

Body weight (BW) is an important trait for meat production in sheep. Over the past few years, numerous quantitative trait loci (QTL) have been detected for production traits in cattle, few QTL studies have been reported for sheep, with even fewer on meat production traits. Body weight (BW) is an important economic trait for meat production. Genome-wide association studies (GWAS) are applied to identify candidate genes for many quantitative traits, in sheep, and in many other species [1,2,3,4,5,6]. GWAS for bovine carcass weight and other production traits have revealed major quantitative trait loci (QTL) on chromosomes (BTA for Bos taurus) BTA6, 8, 11, 14, 24 and 25 [10,11,12]. In brown Swiss cattle, 74 genome-wide significant single nucleotide polymorphisms (SNPs) were shown to be associated with one or more production traits, including fertility, conformation, udder health and workability on BTA6, 11, 24 and 25 [20]

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