Literature DB >> 8099602

Swaledale sheep affected by natural scrapie differ significantly in PrP genotype frequencies from healthy sheep and those selected for reduced incidence of scrapie.

N Hunter1, W Goldmann, G Benson, J D Foster, J Hope.   

Abstract

PrP glycoprotein gene polymorphisms were examined in Swaledale sheep affected by natural scrapie, in healthy sheep and in Swaledales selected for low susceptibility to scrapie. The three groups differed significantly in frequencies of PrP genotypes detected by the restriction enzymes EcoRI, HindIII and BspHI, the latter being indicative of a PrP protein amino acid difference at codon 136. These frequency differences were confirmed in a single-flock study and present good evidence that scrapie susceptibility and resistance are associated with PrP gene variants in Swaledale sheep.

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Year:  1993        PMID: 8099602     DOI: 10.1099/0022-1317-74-6-1025

Source DB:  PubMed          Journal:  J Gen Virol        ISSN: 0022-1317            Impact factor:   3.891


  20 in total

1.  The signature of scrapie: differences in the PrP genotype profile of scrapie-affected and scrapie-free UK sheep flocks.

Authors:  M Baylis; F Houston; W Goldmann; N Hunter; A R McLean
Journal:  Proc Biol Sci       Date:  2000-10-22       Impact factor: 5.349

2.  The PrP genotype of sheep of the improved Valachian breed.

Authors:  L Tkáciková; E Hanusovská; M Novák; M Arvayová; I Mikula
Journal:  Folia Microbiol (Praha)       Date:  2003       Impact factor: 2.099

3.  Diversity in prion protein oligomerization pathways results from domain expansion as revealed by hydrogen/deuterium exchange and disulfide linkage.

Authors:  Frederic Eghiaian; Thorsten Daubenfeld; Yann Quenet; Marieke van Audenhaege; Anne-Pascale Bouin; Guillaume van der Rest; Jeanne Grosclaude; Human Rezaei
Journal:  Proc Natl Acad Sci U S A       Date:  2007-04-18       Impact factor: 11.205

4.  Allelic frequency and genotypes of prion protein at codon 136 and 171 in Iranian Ghezel sheep breeds.

Authors:  Siamak Salami; Reza Ashrafi Zadeh; Mir Davood Omrani; Fatemeh Ramezani; Amir Amniattalab
Journal:  Prion       Date:  2011-07-01       Impact factor: 3.931

5.  Evidence for protein X binding to a discontinuous epitope on the cellular prion protein during scrapie prion propagation.

Authors:  K Kaneko; L Zulianello; M Scott; C M Cooper; A C Wallace; T L James; F E Cohen; S B Prusiner
Journal:  Proc Natl Acad Sci U S A       Date:  1997-09-16       Impact factor: 11.205

6.  Solution structure of a 142-residue recombinant prion protein corresponding to the infectious fragment of the scrapie isoform.

Authors:  T L James; H Liu; N B Ulyanov; S Farr-Jones; H Zhang; D G Donne; K Kaneko; D Groth; I Mehlhorn; S B Prusiner; F E Cohen
Journal:  Proc Natl Acad Sci U S A       Date:  1997-09-16       Impact factor: 11.205

Review 7.  Prions, beta-sheets and transmissible dementias: is there still something missing?

Authors:  P P Liberski
Journal:  Acta Neuropathol       Date:  1995       Impact factor: 17.088

8.  Disulfide mapping reveals the domain swapping as the crucial process of the structural conversion of prion protein.

Authors:  Iva Hafner-Bratkovič; Roman Jerala
Journal:  Prion       Date:  2011-04-01       Impact factor: 3.931

9.  The association of a codon 136 PrP gene variant with the occurrence of natural scrapie.

Authors:  N Hunter; W Goldmann; G Smith; J Hope
Journal:  Arch Virol       Date:  1994       Impact factor: 2.574

10.  Prion protein gene polymorphism in healthy and BSE-affected Slovak cattle.

Authors:  S Hresko; M Mojzis; L Tkacikova
Journal:  J Appl Genet       Date:  2009       Impact factor: 3.240

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