Genome‐wide association study identifies variants in the CAPN9 gene associated with umbilical hernia in pigs. (12th February 2019)

• Record Type: Journal Article
• Authors: Li, X.; Xu, P.; Zhang, C.; Sun, C.; Li, X.; Han, X.; Li, M.; Qiao, R.
• Is Part Of: Animal genetics. Volume 50:Number 2(2019)
• Page Start: 162
• Page End: 165
• Publication Date: 2019-02-12
• Subjects: candidate gene -- genome‐wide association study -- quantitative PCR -- single nucleotide polymorphisms -- Sus scrofa; Animal genetics -- Periodicals; 572.8
• DOI: 10.1111/age.12760
• Languages: English
• ISSNs: 0268-9146

Abstract

Summary: Pig umbilical hernia (UH) affects pig welfare and brings considerable economic loss to the pig industry. To date, the molecular mechanisms underlying pig UH are still poorly understood. To identify potential loci for susceptibility to this disease, we performed a genome‐wide association study in an Erhualian × Shaziling F2 intercross population. A total of 45 animals were genotyped using Illumina Porcine SNP60 BeadChips. We observed a SNP (rs80993347) located in the calpain‐9 ( CAPN9 ) gene on Sus scrofa chromosome 14 that was significantly associated with UH ( P = 1.97 × 10 −10 ). Then, we identified a synonymous mutation rs321865883 (g.20164T>C) in exon 10 of the CAPN9 gene that distinguished two affected individuals (CC) from their normal full‐sibs (TC). Finally, quantitative polymerase chain reaction was explored to investigate the mRNA expression profile of the CAPN9 gene in 12 tissues in Yorkshire pigs at different developmental stages (3, 90 and 180 days). CAPN9 showed high expression levels in the gastrointestinal tract at these three growth stages. The results of this study indicate that the CAPN9 gene might be implicated in UH. Further studies are required to establish a role of CAPN9 in pig UH.