NR AUBY
AU Yu,G.; Chen,J.; Yu,H.; Liu,S.; Chen,J.; Xu,X.; Sha,H.; Zhang,X.; Wu,G.; Xu,S.; Cheng,G.
TI Functional disruption of the prion protein gene in cloned goats
QU Journal of General Virology 2006 Apr; 87(4): 1019-27
PT evaluation studies; journal article
AB The cellular prion protein (PrPc), a membrane glycoprotein anchored to the outer surface of neurons, lymphocytes and other cells, is associated directly with the pathogenesis of the transmissible spongiform encephalopathies (TSEs) occurring mainly in humans, cattle, sheep and goats. Although mice lacking PrPc develop and reproduce normally and are resistant to scrapie infection, large animals lacking PrPc, especially those species in which TSE occurs naturally, are currently not available. Here, five live PRNP+/- goats cloned by gene targeting are reported. Detailed RNA-transcription and protein-expression analysis of one PRNP+/- goat showed that one allele of the caprine PRNP gene had been disrupted functionally. No gross abnormal development or behaviour could be seen in these PRNP+/- goats up to at least 3 months of age. These heterozygous PRNP+/- goats are ready to be used in producing homozygous PRNP-/- goats in which no PrPc should be expressed.
MH Amyloid/genetics; Animals; *Animals, Genetically Modified; Cells, Cultured; Fibroblasts; Goats/*genetics; PrPc Proteins/*genetics/metabolism; Protein Precursors/genetics; Research Support, Non-U.S. Gov't
AD Institute of Biochemistry and Cell Biology, Shanghai Institutes for Biological Sciences, Graduate School of Chinese Academy of Sciences, 320 Yue-Yang Road, Shanghai, 200031, China.
SP englisch
PO England