Abstract

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 r2 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.

Highlights

  • Prion diseases are fatal neurodegenerative disorders that produce an abnormal deleterious prion protein (PrPSc ) from a normal prion protein (PrPC ) [1,2,3,4]

  • We found a total of two novel single nucleotide polymorphisms (SNPs), one nonsynonymous SNP (c.331G > A, A111T) and one synonymous SNP (c.411G > C), in the PRND gene in Jeju and Halla horses

  • We summarized the genetic linkage between prion protein gene (PRNP) and PRND genes in prion disease-susceptible species, including humans, sheep, and goats, and prion disease-resistant species, including dogs and horses

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Summary

Introduction

Prion diseases are fatal neurodegenerative disorders that produce an abnormal deleterious prion protein (PrPSc ) from a normal prion protein (PrPC ) [1,2,3,4]. Genes 2020, 11, 518 the prion protein gene (PRNP), and polymorphisms in the PRNP gene affect the susceptibility of prion diseases in humans and ruminants [5,6,7,8,9,10,11]. Over 40 polymorphisms in the PRNP gene have been reported in goats and sheep. Recent studies have reported that prion disease-resistant species, such as horses in perissodactyls and dogs in carnivores, have distinct genetic features of the PRNP gene [20,21]. Compared with prion disease-susceptible species, dogs have a unique dog-specific amino acid, aspartic acid (D) located at PRNP codon 163, which affects prion resistance [22]. Replacing the dog-specific amino acid D159 and horse-specific amino acid

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