NR ACFL
AU Carlson,G.A.; Ebeling,C.; Yang,S.L.; Telling,G.; Torchia,M.; Groth,D.; Westaway,D.; DeArmond,S.J.; Prusiner,S.B.
TI Prion isolate specified allotypic interactions between the cellular and scrapie prion proteins in congenic and transgenic mice
QU Proceedings of the National Academy of Sciences of the United States of America 1994 Jun 7; 91(12): 5690-4
PT journal article
AB Different prion isolates, often referred to as "strains," present an enigma because considerable evidence argues that prions are devoid of nucleic acid. To investigate prion diversity, we inoculated three "strains" of prions into congenic and transgenic mice harboring variable numbers of two different alleles, designated a and b, of the prion protein (PrP) structural gene, Prn-p. The length of the incubation time was inversely related to the number of Prn-p(a) genes in mice inoculated with the Rocky Mountain Laboratory (RML) prion strain. Results with mice lacking this locus (Prn-p0/0) and transgenic mice argue that long incubation times are not a dominant trait as thought for many years, but rather they are due to reduced levels of the substrate PrPc-A (cellular isoform of PrP, allotype A) in (Prn-p(a) x Prn-pb)F1 mice. In contrast, the Prn-p(a) gene extended incubation times in mice inoculated with the 87V and 22A prion strains, whereas the Prn-pb gene was permissive. Experiments with the 87V isolate suggest that a genetic locus distinct from Prn-p controls deposition of the scrapie isoform of PrP (PrPsc) and attendant neuropathology. Each prion isolate produced distinguishable patterns of PrPsc accumulation in brain; of note, the patterns in Prn-p(a) and Prn-pb congenic mice inoculated with RML prions were more different than those in congenic Prn-pb mice with RML or 22A prions. Our results suggest that scrapie "strain-specific" incubation times can be explained by differences in the relative efficiency of allotypic interactions that lead to conversion of PrPc into PrPsc.
IN Bei congenen und transgenen Mäusen war die Inkubationszeit umso kürzer, je mehr zu den infizierenden Prionproteinen passende Prionproteingene sie besaßen. Umgekehrt wird die Inkubationszeit umso länger, je mehr unpassende Prionproteingene eine Maus besitzt.
MH Alleles; Animal; Brain/metabolism; Mice; Mice, Inbred Strains; Mice, Transgenic; PrPsc Proteins; Prions/*genetics/metabolism/*pathogenicity; Scrapie/*genetics; Support, Non-U.S. Gov't; Support, U.S. Gov't, P.H.S.
AD McLaughlin Research Institute, Great Falls, MT 59405.
SP englisch
PO USA
OR Prion-Krankheiten C