Fine mapping of a QTL on bovine chromosome 6 using imputed full sequence data suggests a key role for the group-specific component (GC) gene in clinical mastitis and milk production. Issue 1 (December 2016)

• Record Type: Journal Article
• Authors: Olsen, Hanne; Knutsen, Tim; Lewandowska-Sabat, Anna; Grove, Harald; Nome, Torfinn; Svendsen, Morten; Arnyasi, Mariann; Sodeland, Marte; Sundsaasen, Kristil; Dahl, Sandra; Heringstad, Bjørg; Hansen, Hanne; Olsaker, Ingrid; Kent, Matthew; Lien, Sigbjørn
• Is Part Of: Genetics, selection, evolution. Volume 48:Issue 1(2016)
• Page Start: 1
• Page End: 16
• Publication Date: 2016-12
• Subjects: Livestock -- Breeding -- Periodicals; Animal genetics -- Periodicals; Livestock -- Genetics -- Periodicals; Evolution -- Periodicals; 576.505
• DOI: 10.1186/s12711-016-0257-2
• Languages: English
• ISSNs: 1297-9686

Abstract

Abstract Background Clinical mastitis is an inflammation of the mammary gland and causes significant costs to dairy production. It is unfavourably genetically correlated to milk production, and, thus, knowledge of the mechanisms that underlie these traits would be valuable to improve both of them simultaneously through breeding. A quantitative trait locus (QTL) that affects both clinical mastitis and milk production has recently been fine-mapped to around 89 Mb on bovine chromosome 6 (BTA6), but identification of the gene that underlies this QTL was not possible due to the strong linkage disequilibrium between single nucleotide polymorphisms (SNPs) within this region. Our aim was to identify the gene and, if possible, the causal polymorphism(s) responsible for this QTL through association analysis of high-density SNPs and imputed full sequence data in combination with analyses of transcript and protein levels of the identified candidate gene. Results Associations between SNPs and the studied traits were strongest for SNPs that were located within and immediately upstream of thegroup -specific component (GC ) gene. This gene encodes the vitamin D-binding protein (DBP) and has multiple roles in immune defense and milk production. A 12-kb duplication that was identified downstream of this gene covered its last exon and segregated with the QTL allele that is associated with increased mastitis susceptibility and milk production. However, analyses ofGC mRNA levels on the available samples revealed no differences in expression between animals having or lacking this duplication. Moreover, we detected no differences in the concentrations of DBP and its ligand vitamin D between the animals with differentGC genotypes that were available for this study. Conclusions Our results suggestGC as the gene that underlies the QTL for clinical mastitis and milk production. However, since only healthy animals were sampled for transcription and expression analyses, we could not draw any final conclusion on the absence of quantitative differences between animals with different genotypes. Future studies should investigateGC RNA expression and protein levels in cows with different genotypes during an infection.