Abstract

ObjectivePreviously, we reported quantitative trait loci (QTLs) affecting backfat thickness (BFT) traits on pig chromosome 5 (SW1482–SW963) in an F2 intercross population between Landrace and Korean native pigs. The aim of this study was to evaluate glutamate receptor-interacting protein 1 (GRIP1) as a positional candidate gene underlying the QTL affecting BFT traits.MethodsGenotype and phenotype analyses were performed using the 1,105 F2 progeny. A mixed-effect linear model was used to access association between these single nucleotide polymorphism (SNP) markers and the BFT traits in the F2 intercross population.ResultsHighly significant associations of two informative SNPs (c.2442 T>C, c.3316 C>G [R1106G]) in GRIP1 with BFT traits were detected. In addition, the two SNPs were used to construct haplotypes that were also highly associated with the BFT traits.ConclusionThe SNPs and haplotypes of the GRIP1 gene determined in this study can contribute to understand the genetic structure of BFT traits in pigs.

Highlights

  • Glutamate receptor interacting protein 1 is encoded by the glutamate receptorinteracting protein 1 (GRIP1) gene in human [14]

  • The association between single nucleotide polymorphism (SNP) markers within the exons of GRIP1 and backfat thickness (BFT)-related traits in pigs is worthy of investigation

  • We presents the association of BFT traits with the GRIP1 gene using an F2 intercross population between Korean native pigs (KNP) and Landrace pigs

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Summary

Objective

We reported quantitative trait loci (QTLs) affecting backfat thickness (BFT) traits on pig chromosome 5 (SW1482–SW963) in an F2 intercross population between Landrace and Korean native pigs. The aim of this study was to evaluate glutamate receptorinteracting protein 1 (GRIP1) as a positional candidate gene underlying the QTL affecting BFT traits. A mixed-effect linear model was used to access association between these single nucleotide polymorphism (SNP) markers and the BFT traits in the F2 intercross population. C>G [R1106G]) in GRIP1 with BFT traits were detected. The two SNPs were used to construct haplotypes that were highly associated with the BFT traits. Conclusion: The SNPs and haplotypes of the GRIP1 gene determined in this study can contri­ bute to understand the genetic structure of BFT traits in pigs

INTRODUCTION
MATERIALS AND METHODS
RESULTS AND DISCUSSION
CONFLICT OF INTEREST
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