Search for genomic regions carrying the lethal genetic variants in the Duroc pigs

The necessity to address the problem of reducing embryonic losses, which in pigs are estimated at the level up to 30 %, is not in doubt. LoF (Loss of Function) mutations, which in the homozygous state can lead to the termination of synthesis or synthesis of non-functional proteins, are considered as one of the genetic factors that cause embryonic mortality. While in cattle, an intensive search for LoF mutations is carried out, in pigs, studies of such mutations are still performed on a smaller scale. Whole-genome analysis using medium- and high-density SNP chips which are uniformly covering the entire genome allows researchers to apply new approaches to identify positional candidates for lethal recessive variants. One of such approaches is the analysis of the level of the linkage disequilibrium (LD) of alleles of SNP markers. The aim of our research was to search for genomic regions that carry presumed lethal recessive variants in Duroc pigs, based on the analysis of the linkage disequilibrium of alleles in SNP loci. Studies were carried out with 715 Duroc boars bred in JSC Top Gen (Voronezh region) in 2017-2019. Whole-genome genotyping was carried out using Porcine GGP HD DNA chips (Neogene/Illumina Inc., USA) containing about 70 thousand SNP. After the quality control, 42981 polymorphic SNP were selected for analysis. Search of reference sequences (rs) and clarification of their localization was carried out using the Ensembl database (http://www.ensembl.org). Functional gene annotations were performed using the GeneCards database (http://www.genecards.org/). Analysis of the maintenance of genetic equilibrium showed the presence of 990 SNPs with the absence of one of the homozygous genotypes (2.30 % of the total number of polymorphic SNPs), which were distributed among all pig chromosomes, including 205 SNPs, which were in the linkage disequilibrium (0.48 %). Chromosomes SSC9 (0.8 %), SSC5 (0.77 %), SSC7 (0.68 %) and SSC2 (0.68 %) were characterized by the highest ratio of SNPs in linkage disequilibrium, while chromosomes SSC13 (0.28 %), SSC4 (0.29 %) and SSC10 (0.30 %) were the lowest. For 52 SNPs, of which 25 SNPs were localized within genes, differences in observed and expected heterozygosity frequencies were statistically significant (p function show_eabstract() { $('#eabstract1').hide(); $('#eabstract2').show(); $('#eabstract_expand').hide(); }