Abstract

BackgroundPrion protein (PrP) level plays the central role in bovine spongiform encephalopathy (BSE) susceptibility. Increasing the level of PrP decreases incubation period for this disease. Therefore, studying the expression of the cellular PrP or at least the messenger RNA might be used in selection for preventing the propagation of BSE and other prion diseases. Two insertion/deletion (indel) variations have been tentatively associated with susceptibility/resistance of cattle to classical BSE.Methodology/Principal FindingsWe studied the expression of each genotype at the two indel sites in Japanese Black (JB) and Japanese Brown (JBr) cattle breeds by a standard curve method of real-time PCR. Five diplotypes subdivided into two categories were selected from each breed. The two cattle breeds were considered differently. Expression of PRNP was significantly (p<0.0001) greater in the homozygous deletion genotype at the 23-bp locus in JB breed. Compared to the homozygous genotypes, the expression of PRNP was significantly greater in the heterozygous genotype at the 12-bp locus in JB (p<0.0001) and in JBr (p = 0.0394) breeds. In addition, there was a statistical significance in the PRNP levels between the insertion and the deletion alleles of the 23-bp locus in JB (p = 0.0003) as well as in JBr (p = 0.0032). There was no significance in relation to sex, age, geographical location or due to their interactions (p>0.05).ConclusionOur results suggest that the del/del genotype or at least its del allele may modulate the expression of PRNP at the 23-bp locus in the medulla oblongata of these cattle breeds.

Highlights

  • Genetic variations in the prion protein gene (PRNP) are linked to the occurrence of transmissible spongiform encephalopathies (TSEs) called prion diseases in humans, sheep and mice [1,2,3,4]

  • Our results suggest that the del/del genotype or at least its del allele may modulate the expression of PRNP at the 23-bp locus in the medulla oblongata of these cattle breeds

  • Polymorphisms in two regulatory regions in the bovine PRNP have been tentatively associated with classical bovine spongiform encephalopathy (BSE) incidences in a few cattle populations [6,7,8]

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Summary

Introduction

Genetic variations in the prion protein gene (PRNP) are linked to the occurrence of transmissible spongiform encephalopathies (TSEs) called prion diseases in humans, sheep and mice [1,2,3,4]. Polymorphisms in two regulatory regions in the bovine PRNP have been tentatively associated with classical BSE (cBSE) incidences in a few cattle populations [6,7,8]. Expression of the cellular PrP is necessary for the transmission and propagation of prion diseases [9]. Based on reporter gene assays, increased level of PrP decreases the incubation period for cBSE [10]. Prion protein (PrP) level plays the central role in bovine spongiform encephalopathy (BSE) susceptibility. Studying the expression of the cellular PrP or at least the messenger RNA might be used in selection for preventing the propagation of BSE and other prion diseases. Two insertion/deletion (indel) variations have been tentatively associated with susceptibility/resistance of cattle to classical BSE

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