Abstract
BackgroundCalving difficulty and perinatal mortality are prevalent in modern-day cattle production systems. It is well-established that there is a genetic component to both traits, yet little is known about their underlying genomic architecture, particularly in beef breeds. Therefore, we performed a genome-wide association study using high-density genotypes to elucidate the genomic architecture of these traits and to identify regions of the bovine genome associated with them.ResultsGenomic regions associated with calving difficulty (direct and maternal) and perinatal mortality were detected using two statistical approaches: (1) single-SNP (single nucleotide polymorphism) regression and (2) a Bayesian approach. Data included high-density genotypes on 770 Holstein-Friesian, 927 Charolais and 963 Limousin bulls. Several novel or previously identified genomic regions were detected but associations differed by breed. For example, two genomic associations, one each on chromosomes 18 and 2 explained 2.49 % and 3.13 % of the genetic variance in direct calving difficulty in the Holstein-Friesian and Charolais populations, respectively. Imputed Holstein-Friesian sequence data was used to refine the genomic regions responsible for significant associations. Several candidate genes on chromosome 18 were identified and four highly significant missense variants were detected within three of these genes (SIGLEC12, CTU1, and ZNF615). Nevertheless, only CTU1 contained a missense variant with a putative impact on direct calving difficulty based on SIFT (0.06) and Polyphen (0.95) scores. Using imputed sequence data, we refined a genomic region on chromosome 4 associated with maternal calving difficulty in the Holstein-Friesian population and found the strongest association with an intronic variant in the PCLO gene. A meta-analysis was performed across the three breeds for each calving performance trait to identify common variants associated with these traits in the three breeds. Our results suggest that a portion of the genetic variation in calving performance is common to all three breeds.ConclusionThe genomic architecture of calving performance is complex and mainly influenced by many polymorphisms of small effect. We identified several associations of moderate effect size but the majority were breed-specific, indicating that breed-specific alleles exist for calving performance or that the linkage phase between genotyped allele and causal mutation varies between breeds.Electronic supplementary materialThe online version of this article (doi:10.1186/s12711-015-0126-4) contains supplementary material, which is available to authorized users.
Highlights
Calving difficulty and perinatal mortality are prevalent in modern-day cattle production systems
The objective of this study was to perform a genome-wide association studies (GWAS) based on genotypes obtained with the Illumina bovine high-density BeadChip that comprises 777 962 SNPs, to identify regions of the genome associated with three calving performance traits: (i) direct calving difficulty, (ii) maternal calving difficulty and (iii) direct perinatal mortality, in three cattle breeds (Holstein-Friesian, Charolais and Limousin) and to refine the detected genomic regions using whole-genome sequence data
Maternal calving difficulty In spite of the small size of the population analysed for maternal calving difficulty, our results suggest that this trait may be influenced by many polymorphisms each of small effect since the maximum proportion of the genetic variation accounted for by any one SNP was 0.13 %
Summary
Calving difficulty and perinatal mortality are prevalent in modern-day cattle production systems. It is well-established that there is a genetic component to both traits, yet little is known about their underlying genomic architecture, in beef breeds. It is important to determine the number of variants and the size of their effects on calving difficulty and perinatal mortality to increase the accuracy of genomic predictions. Quantitative trait loci (QTL) associated with calving difficulty and perinatal mortality in cattle have been identified by genome-wide association studies (GWAS) and are mainly concentrated on chromosomes 6, 11, 12, 18 and 28 [11,12,13]; these studies focused mainly on dairy cattle breeds
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