Absence of Strong Genetic Linkage Disequilibrium between Single Nucleotide Polymorphisms (SNPs) in the Prion Protein Gene (PRNP) and the Prion-Like Protein Gene (PRND) in the Horse, a Prion-Resistant Species

被引:7
作者
Won, Sae-Young [1 ,2 ]
Kim, Yong-Chan [1 ,2 ]
Do, Kyoungtag [3 ]
Jeong, Byung-Hoon [1 ,2 ]
机构
[1] Jeonbuk Natl Univ, Korea Zoonosis Res Inst, Iksan 54531, Jeonbuk, South Korea
[2] Jeonbuk Natl Univ, Dept Bioact Mat Sci, Jeonju 54896, Jeonbuk, South Korea
[3] Jeju Natl Univ, Fac Biotechnol, Dept Anim Biotechnol, Lab Equine Sci, Jeju 63243, South Korea
基金
新加坡国家研究基金会;
关键词
prion; polymorphisms; single nucleotide polymorphisms; prion-like protein gene; Doppel; PRND; PRNP; CREUTZFELDT-JAKOB-DISEASE; PRP GENE; SCRAPIE; SHEEP; ASSOCIATION; MUTATION; LOOP;
D O I
10.3390/genes11050518
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Prion disease is a fatal neurodegenerative disorder caused by a deleterious prion protein (PrPSc). However, prion disease has not been reported in horses during outbreaks of transmissible spongiform encephalopathies (TSEs) in various animals in the UK. In previous studies, single nucleotide polymorphisms (SNPs) in the prion protein gene (PRNP) have been significantly associated with susceptibility to prion disease, and strong linkage disequilibrium (LD) between PRNP and prion-like protein gene (PRND) SNPs has been identified in prion disease-susceptible species. On the other hand, weak LD values have been reported in dogs, a prion disease-resistant species. In this study, we investigated SNPs in the PRND gene and measured the LD values between the PRNP and PRND SNPs and the impact of a nonsynonymous SNP found in the horse PRND gene. To identify SNPs in the PRND gene, we performed direct sequencing of the PRND gene. In addition, to assess whether the weak LD value between the PRNP and PRND SNPs is a characteristic of prion disease-resistant animals, we measured the LD value between the PRNP and PRND SNPs using D' and r(2) values. Furthermore, we evaluated the impact of a nonsynonymous SNP in the Doppel protein with PolyPhen-2, PROVEAN, and PANTHER. We observed two novel SNPs, c.331G > A (A111T) and c.411G > C. The genotype and allele frequencies of the c.331G > A (A111T) and c.411G > C SNPs were significantly different between Jeju, Halla, and Thoroughbred horses. In addition, we found a total of three haplotypes: GG, AG, and GC. The GG haplotype was the most frequently observed in Jeju and Halla horses. Furthermore, the impact of A111T on the Doppel protein was predicted to be benign by PolyPhen-2, PROVEAN, and PANTHER. Interestingly, a weak LD value between the PRNP and PRND SNPs was found in the horse, a prion disease-resistant animal. To the best of our knowledge, these results suggest that a weak LD value could be one feature of prion disease-resistant animals.
引用
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页数:12
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