Association of a missense mutation in the positional candidate gene glutamate receptor-interacting protein 1 with backfat thickness traits in pigsopen access
- Authors
- Lee, Jae-Bong; Park, Hee-Bok; Yoo, Chae-Kyoung; Kim, Hee-Sung; Cho, In-Cheol; Lim, Hyun-Tae
- Issue Date
- Aug-2017
- Publisher
- ASIAN-AUSTRALASIAN ASSOC ANIMAL PRODUCTION SOC
- Keywords
- Glutamate Receptor-interacting Protein 1 (GRIP1); Backfat; Quantitative Trait Loci (QTL); Landrace; Korean Native Pigs
- Citation
- ASIAN-AUSTRALASIAN JOURNAL OF ANIMAL SCIENCES, v.30, no.8, pp 1081 - 1085
- Pages
- 5
- Indexed
- SCIE
SCOPUS
KCI
- Journal Title
- ASIAN-AUSTRALASIAN JOURNAL OF ANIMAL SCIENCES
- Volume
- 30
- Number
- 8
- Start Page
- 1081
- End Page
- 1085
- URI
- https://scholarworks.gnu.ac.kr/handle/sw.gnu/13558
- DOI
- 10.5713/ajas.16.0414
- ISSN
- 1011-2367
1976-5517
- Abstract
- Objective: Previously, 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. Methods: Genotype 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. Results: Highly 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. Conclusion: The SNPs and haplotypes of the GRIP1 gene determined in this study can contribute to understand the genetic structure of BFT traits in pigs.
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