4.6 Article

Fine Mapping of a Major Backfat QTL Reveals a Causal Regulatory Variant Affecting the CCND2 Gene

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FRONTIERS IN GENETICS
卷 13, 期 -, 页码 -

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FRONTIERS MEDIA SA
DOI: 10.3389/fgene.2022.871516

关键词

GWAS; pig genomics; animal breeding; finemapping; backfat

资金

  1. Instituto Nacional de Ciencia e Tecnologia de Ciencia Animal (INCT-CA), Coordenacao de Aperfeicoamento de Pessoal de Nivel Superior (CAPES) [465377/2014-9]

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Backfat is an important trait in pork production, and excessive fat can result in economic losses. Through genome-wide association analysis, we identified a QTL for backfat thickness located within the third intron of the CCND2 gene, and further discovered core haplotypes associated with low backfat.
Backfat is an important trait in pork production, and it has been included in the breeding objectives of genetic companies for decades. Although adipose tissue is a good energy storage, excessive fat results in reduced efficiency and economical losses. A large QTL for backfat thickness on chromosome 5 is still segregating in different commercial pig breeds. We fine mapped this QTL region using a genome-wide association analysis (GWAS) with 133,358 genotyped animals from five commercial populations (Landrace, Pietrain, Large White, Synthetic, and Duroc) imputed to the porcine 660K SNP chip. The lead SNP was located at 5:66103958 (G/A) within the third intron of the CCND2 gene, with the G allele associated with more backfat, while the A allele is associated with less backfat. We further phased the QTL region to discover a core haplotype of five SNPs associated with low backfat across three breeds. Linkage disequilibrium analysis using whole-genome sequence data revealed three candidate causal variants within intronic regions and downstream of the CCND2 gene, including the lead SNP. We evaluated the association of the lead SNP with the expression of the genes in the QTL region (including CCND2) in a large cohort of 100 crossbred samples, sequenced in four different tissues (lung, spleen, liver, muscle). Results show that the A allele increases the expression of CCND2 in an additive way in three out of four tissues. Our findings indicate that the causal variant for this QTL region is a regulatory variant within the third intron of the CCND2 gene affecting the expression of CCND2.

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