{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,6]],"date-time":"2026-10-06T13:04:32Z","timestamp":1791291872437,"version":"4.1.0"},"reference-count":140,"publisher":"Canadian Science Publishing","issue":"5","license":[{"start":{"date-parts":[[2001,10,1]],"date-time":"2001-10-01T00:00:00Z","timestamp":1001894400000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/www.nrcresearchpress.com\/page\/about\/CorporateTextAndDataMining"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Biochem. Cell Biol."],"published-print":{"date-parts":[[2001,10,1]]},"abstract":"<jats:p> The prion protein gene Prnp encodes PrP<jats:sup>Sc<\/jats:sup>, the major structural component of prions, infectious pathogens causing a number of disorders including scrapie and bovine spongiform encephalopathy (BSE). Missense mutations in the human Prnp gene, PRNP, cause inherited prion diseases such as familial Creutzfeldt\u0096Jakob Disease. In uninfected animals, Prnp encodes a GPI-anchored protein denoted PrP<jats:sup>C<\/jats:sup>, and in prion infections, PrP<jats:sup>C<\/jats:sup> is converted to PrP<jats:sup>Sc<\/jats:sup> by templated refolding. Although Prnp is conserved in mammalian species, attempts to verify interactions of putative PrP-binding proteins by genetic means have proven frustrating in that two independent lines of Prnp gene ablated mice (Prnp<jats:sup>0\/0<\/jats:sup> mice: ZrchI and Npu) lacking PrP<jats:sup>C<\/jats:sup> remain healthy throughout development. This indicates that PrP<jats:sup>C<\/jats:sup> serves a function that is not apparent in a laboratory setting or that other molecules have overlapping functions. Shuttling or sequestration of synaptic Cu(II) via binding to N-terminal octapeptide residues and (or) signal transduction involving the fyn kinase are possibilities currently under consideration. A new point of entry into the issue of prion protein function has emerged from identification of a paralog, Prnd, with 25% coding sequence identity to Prnp. Prnd lies downstream of Prnp and encodes the Dpl protein. Like PrP<jats:sup>C<\/jats:sup>, Dpl is presented on the cell surface via a GPI anchor and has three \u03b1-helices: however, it lacks the conformationally plastic and octapeptide repeat domains present in its well-known relative. Interestingly, Dpl is overexpressed in two other lines of Prnp<jats:sup>0\/0<\/jats:sup> mice (Ngsk and Rcm0) via intergenic splicing events. These lines of Prnp<jats:sup>0\/0<\/jats:sup> mice exhibit ataxia and apoptosis of cerebellar cells, indicating that ectopic synthesis of Dpl protein is toxic to CNS neurons: this inference has now been confirmed by the construction of transgenic mice expressing Dpl under the direct control of the PrP promoter. Remarkably, Dpl-programmed ataxia is rescued by wt Prnp transgenes. The interaction between the Prnp and Prnd genes in mouse cerebellar neurons may have a physical correlate in competition between Dpl and PrP<jats:sup>C<\/jats:sup> within a common biochemical pathway that, when misregulated, leads to apoptosis.Key words: spongiform encephalopathy, neurodegenerative disease, paralogs, scrapie, CJD. <\/jats:p>","DOI":"10.1139\/o01-142","type":"journal-article","created":{"date-parts":[[2011,4,23]],"date-time":"2011-04-23T02:37:18Z","timestamp":1303526238000},"page":"613-628","source":"Crossref","is-referenced-by-count":13,"title":["Biology of the prion gene complex"],"prefix":"10.1139","volume":"79","author":[{"given":"Peter","family":"Mastrangelo","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"David","family":"Westaway","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"155","reference":[{"key":"p_22\/p_22_1","doi-asserted-by":"crossref","first-page":"417","DOI":"10.1016\/0092-8674(86)90662-8","volume":"46","author":"Basler K.","year":"1986","journal-title":"Cell"},{"key":"p_23\/p_23_1","doi-asserted-by":"crossref","first-page":"125","DOI":"10.1093\/protein\/1.2.125","volume":"1","author":"Bazan J.F.","year":"1987","journal-title":"Protein Eng."},{"key":"p_24\/p_24_1","doi-asserted-by":"crossref","first-page":"347","DOI":"10.1093\/embo-reports\/kve088","volume":"2","author":"Behrens A.","year":"2001","journal-title":"EMBO Rep."},{"key":"p_25\/p_25_1","doi-asserted-by":"crossref","first-page":"329","DOI":"10.1099\/0022-1317-73-2-329","volume":"73","author":"Bessen R.A.","year":"1992","journal-title":"J. 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