Muscle glycogen level and occurrence of acid meat in commercial hybrid pigs are regulated by two low-frequency causal variants with large effects and multiple common variants with small effects

• Published in: Genetics selection evolution (Paris) 2019-08, Vol.51 (1), p.46-46, Article 46
• Main Authors: Liu, Xianxian, Zhou, Lisheng, Xie, Xianhua, Wu, Zhongzi, Xiong, Xinwei, Zhang, Zhiyan, Yang, Jie, Xiao, Shijun, Zhou, Mengqing, Ma, Junwu, Huang, Lusheng
• Format: Article
• Language: English
• Subjects: Alleles; AMP-Activated Protein Kinases - genetics; Animals; Annotations; Association analysis; Chromosomes; Cohort Studies; Female; Food Quality; Gene frequency; Gene mapping; Genes; Genetic aspects; Genetic research; Genetic Variation; Genome-wide association studies; Genome-Wide Association Study - veterinary; Genomes; Genomics; Glucose; Glycogen; Glycogen - metabolism; Hogs; Kinases; Life Sciences; Male; Meat; Meat - analysis; Meat industry; Meat production; Methods; Missense mutation; Muscle, Skeletal - metabolism; Muscles; Mutation; Mutation, Missense; Parenting; Phosphorylase Kinase - genetics; Polymorphism, Single Nucleotide; Polysaccharides; Population genetics; Pork; Pork industry; Protein Subunits - genetics; Quantitative genetics; Quantitative Trait Loci; Scaffolds; Single-nucleotide polymorphism; Species Specificity; Sus scrofa; Swine; Swine - genetics; Swine - metabolism; Swine breeding; Vitamin E
• ISSN: 1297-9686; 0999-193X; 1297-9686
• DOI: 10.1186/s12711-019-0488-0

Meat production from the commercial crossbred Duroc × (Landrace × Yorkshire) (DLY) pig is predominant in the pork industry, but its meat quality is often impaired by low ultimate pH (pHu). Muscle glycogen level at slaughter is closely associated with pHu and meat technological quality, but its genetic basis remains elusive. The aim of this study was to identify genes and/or causative mutations associated with muscle glycogen level and other meat quality traits by performing a genome-wide association study (GWAS) and additional analyses in a population of 610 DLY pigs. Our initial GWAS identified a genome-wide significant (P = 2.54e-11) quantitative trait locus (QTL) on SSC15 (SSC for Sus scrofa chromosome) for the level of residual glycogen and glucose (RG) in the longissimus muscle at 45 min post-mortem. Then, we demonstrated that a low-frequency (minor allele frequency = 0.014) R200Q missense mutation in the PRKAG3 (RN) gene caused this major QTL effect on RG. Moreover, we showed that the 200Q (RN ) allele was introgressed from the Hampshire breed into more than one of the parental breeds of the DLY pigs. After conditioning on R200Q, re-association analysis revealed three additional QTL for RG on SSC3 and 4, and on an unmapped scaffold (AEMK02000452.1). The SSC3 QTL was most likely caused by a splice mutation (g.8283C>A) in the PHKG1 gene that we had previously identified. Based on functional annotation, the genes TMCO1 on SSC4 and CKB on the scaffold represent promising candidate genes for the other two QTL. There were significant interaction effects of the GWAS tag SNPs at those two loci with PRKAG3 R200Q on RG. In addition, a number of common variants with potentially smaller effects on RG (P A. We found that the RN allele segregates in the parental lines of our DLY population and strongly influences its meat quality. Our findings also indicate that the genetic basis of RG in DLY can be mainly attributed to two major genes (PRKAG3 and PHKG1), along with many minor genes.