NR AHOC
AU Lowenstein,D.H.; Butler,D.A.; Westaway,D.; McKinley,M.P.; DeArmond,S.J.; Prusiner,S.B.
TI Three hamster species with different scrapie incubation times and neuropathological features encode distinct prion proteins
QU Molecular and Cellular Biology 1990 Mar; 10(3): 1153-63
PT journal article
AB Given the critical role of the prion protein (PrP) in the transmission and pathogenesis of experimental scrapie, we investigated the PrP gene and its protein products in three hamster species, Chinese (CHa), Armenian (AHa), and Syrian (SHa), each of which were found to have distinctive scrapie incubation times. Passaging studies demonstrated that the host species, and not the source of scrapie prions, determined the incubation time for each species, and histochemical studies of hamsters with clinical signs of scrapie revealed characteristic patterns of neuropathology. Northern (RNA) analysis showed the size of PrP mRNA from CHa, AHa, and SHa hamsters to be 2.5, 2.4, and 2.1 kilobases, respectively. Immunoblotting demonstrated that the PrP isoforms were of similar size (33 to 35 kilodaltons); however, the monoclonal antibody 13A5 raised against SHa PrP did not react with the CHa or AHa PrP molecules. Comparison of the three predicted amino acid sequences revealed that each is distinct. Furthermore, differences within the PrP open reading frame that uniquely distinguish the three hamster species are within a hydrophilic segment of 11 amino acids that includes polymorphisms linked to scrapie incubation times in inbred mice and an inherited prion disease of humans. Single polymorphisms in this region correlate with the presence or absence of amyloid plaques for a given hamster species or mouse inbred strain. Our findings demonstrate distinctive molecular, pathological, and clinical characteristics of scrapie in three related species and are consistent with the hypothesis that molecular properties of the host PrP play a pivotal role in determining the incubation time and neuropathological features of scrapie.
MH Animal; Base Sequence; Blotting, Northern; Blotting, Southern; Blotting, Western; Cloning, Molecular; Comparative Study; Cricetulus/genetics; Hamsters; Mesocricetus/genetics; Molecular Sequence Data; Oligonucleotides; Polymerase Chain Reaction; Prions/*genetics/metabolism; RNA, Messenger/genetics; Restriction Mapping; Scrapie/*genetics/pathology; Species Specificity; Support, Non-U.S. Gov't; Support, U.S. Gov't, P.H.S.
AD Department of Neurology, University of California, San Francisco 94143-0518.
SP englisch
PO USA