Veterinary Research · 2012 · 83 citations · 16 references
Veterinary MedicineAnimal SciencesInfectious DiseasesNeurodegenerationPrion DiseasesTransgenic Animal ModelsAnimal Prion DiseasesCreutzfeldt-jakob DiseaseGoat Infectious DiseasesNeuropathology Of Prion DiseasePrion Protein MisfoldingPrion Protein StructureBovine Spongiform Encephalopathy NeuropathologyNonsense Mutation EffectsPrion Disease ModelsPrion Disease PathologyPrion PathogenesisPrion Protein DepositionPrion Protein FoldingTransgenic Animals
Prion diseases such as scrapie in small ruminants, bovine spongiform encephalopathy (BSE) in cattle and Creutzfeldt-Jakob disease (CJD) in man, are fatal neurodegenerative disorders. These diseases result from the accumulation of misfolded conformers of the host-encoded prion protein (PrP) in the central nervous system. To date naturally-occurring PrP free animals have not been reported. Here we describe healthy non-transgenic animals, Norwegian Dairy Goats, lacking prion protein due to a nonsense mutation early in the gene. These animals are predicted to be resistant to prion disease and will be valuable for research and for production of prion-free products.
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Mice devoid of PrP are resistant to scrapie
Hansruedi Büeler, Adriano Aguzzi, Andreas W. Sailer et al. · Cell · 1993 · 2.1K citations · Full text
Cellular prion protein mediates impairment of synaptic plasticity by amyloid-β oligomers
Juha Laurén, David A. Gimbel, Haakon B. Nygaard et al. · Nature · 2009 · 1.5K citations · Full text
Production of cattle lacking prion protein
Jürgen A. Richt, Poothappillai Kasinathan, Amir N. Hamir et al. · Nature Biotechnology · 2006 · 345 citations · Full text