Abstract

BackgroundThe current availability of genotypes for very large numbers of single nucleotide polymorphisms (SNPs) is leading to more accurate estimates of inbreeding coefficients and more detailed approaches for detecting inbreeding depression. In the present study, genome-wide information was used to detect inbreeding depression for two reproductive traits (total number of piglets born and number of piglets born alive) in an ancient strain of Iberian pigs (the Guadyerbas strain) that is currently under serious danger of extinction.MethodsA total of 109 sows with phenotypic records were genotyped with the PorcineSNP60 BeadChip v1. Inbreeding depression was estimated using a bivariate animal model in which the inbreeding coefficient was included as a covariate. We used two different measures of genomic inbreeding to perform the analyses: inbreeding estimated on a SNP-by-SNP basis and inbreeding estimated from runs of homozygosity. We also performed the analyses using pedigree-based inbreeding.ResultsSignificant inbreeding depression was detected for both traits using all three measures of inbreeding. Genome-wide information allowed us to identify one region on chromosome 13 associated with inbreeding depression. This region spans from 27 to 54 Mb and overlaps with a previously detected quantitative trait locus and includes the inter-alpha-trypsin inhibitor gene cluster that is involved with embryo implantation.ConclusionsOur results highlight the value of high-density SNP genotyping for providing new insights on where genes causing inbreeding depression are located in the genome. Genomic measures of inbreeding obtained on a SNP-by-SNP basis or those based on the presence/absence of runs of homozygosity represent a suitable alternative to pedigree-based measures to detect inbreeding depression, and a useful tool for mapping studies. To our knowledge, this is the first study in domesticated animals using the SNP-by-SNP inbreeding coefficient to map specific regions within chromosomes associated with inbreeding depression.Electronic supplementary materialThe online version of this article (doi:10.1186/s12711-014-0081-5) contains supplementary material, which is available to authorized users.

Highlights

  • The current availability of genotypes for very large numbers of single nucleotide polymorphisms (SNPs) is leading to more accurate estimates of inbreeding coefficients and more detailed approaches for detecting inbreeding depression

  • Fped = pedigree-based inbreeding; Fsnp_r = genomic SNP-by-SNP inbreeding estimated as the proportion of homozygous genotypes; Fsnp = genomic SNP-by-SNP inbreeding based on the excess of SNP homozygosity; Froh = genomic inbreeding based on all runs of homozygosity (ROH); Froh_short = genomic inbreeding based on short ROH; Froh_long = genomic inbreeding based on long ROH

  • NBA = number of piglets born alive; TNB = total number of piglets born; results are expressed as the change in phenotypic mean per 10% increase in F; Fsnp = genomic SNP-by-SNP inbreeding based on the excess of SNP homozygosity; Froh = genomic inbreeding based on all ROH; Froh_short = genomic inbreeding based on short ROH; Froh_long = genomic inbreeding based on long ROH; significant values are indicated with asterisk (*p < 0.05, **p < 0.01)

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Summary

Introduction

The current availability of genotypes for very large numbers of single nucleotide polymorphisms (SNPs) is leading to more accurate estimates of inbreeding coefficients and more detailed approaches for detecting inbreeding depression. An alternative approach for quantifying individual homozygosity that better reflects IBD is based on runs of homozygosity (ROH). The idea is that autozygous genotypes are not evenly distributed throughout the genome but are distributed in runs that are inherited together [7,8]. This is explained by consanguineous matings causing inheritance of haplotypes that are IBD and result in homozygous stretches along the genome of the offspring [9]. It has been shown that these runs provide a good measure of individual genome-wide autozygosity (Froh) and allow us to distinguish between recent and ancient inbreeding [10]

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