Prion transmission from humans to transgenic mice expression chimeric human mouse prion protein provides evidence for a species-specific factor in prion propagation
Telling, G.C.; Scott, M.; Schatzl, H.; Foster, D.; Yang, S.L.; Torchia, M.; Cohen, F.E.; Dearmond, S.J.; Prusiner, S.B.
Molecular Biology of the Cell 5(Suppl ): 473A
1994
ISSN/ISBN: 1059-1524
Accession: 032956114
PDF emailed within 1 workday: $29.90
Related References
Telling, G.C.; Mastrianni, J.A.; Dearmond, S.J.; Prusiner, S.B. 1996: Exploring mechanisms of prion propagation using mice expressing human and chimeric mouse/human prion protein transgenes Neurology 46(2 Suppl): A251Telling, G.C.; Scott, M.; Hsiao, K.K.; Foster, D.; Yang, S.L.; Torchia, M.; Sidle, K.C.; Collinge, J.; DeArmond, S.J.; Prusiner, S.B. 1994: Transmission of Creutzfeldt-Jakob disease from humans to transgenic mice expressing chimeric human-mouse prion protein Proceedings of the National Academy of Sciences of the United States of America 91(21): 9936-9940
Race, B.; Williams, K.; Hughson, A.G.; Jansen, C.; Parchi, P.; Rozemuller, A.J.M.; Chesebro, B. 2018: Familial human prion diseases associated with prion protein mutations Y226X and G131V are transmissible to transgenic mice expressing human prion protein Acta Neuropathologica Communications 6(1): 13
Schmitz, M.; Lüllmann, K.; Zafar, S.; Ebert, E.; Wohlhage, M.; Oikonomou, P.; Schlomm, M.; Mitrova, E.; Beekes, M.; Zerr, I. 2014: Association of prion protein genotype and scrapie prion protein type with cellular prion protein charge isoform profiles in cerebrospinal fluid of humans with sporadic or familial prion diseases Neurobiology of Aging 35(5): 1177-1188
Telling, G.C.; Tremblay, P.; Torchia, M.; Dearmond, S.J.; Cohen, F.E.; Prusiner, S.B. 1997: N-terminally tagged prion protein supports prion propagation in transgenic mice Protein Science: a Publication of the Protein Society 6(4): 825-833
Serra, F.; Dudas, S.; Torres, J.M.; Anderson, R.; Oevermann, A.; Espinosa, J.C.; Czub, S.; Seuberlich, T. 2018: Presumptive BSE cases with an aberrant prion protein phenotype in Switzerland, 2011: Lack of prion disease in experimentally inoculated cattle and bovine prion protein transgenic mice Transboundary and Emerging Diseases 65(5): 1348-1356
Supattapone, S.; Bosque, P.; Muramoto, T.; Wille, H.; Aagaard, C.; Peretz, D.; Nguyen, H.O.; Heinrich, C.; Torchia, M.; Safar, J.; Cohen, F.E.; DeArmond, S.J.; Prusiner, S.B.; Scott, M. 1999: Prion protein of 106 residues creates an artifical transmission barrier for prion replication in transgenic mice Cell 96(6): 869-878
Norstrom, E.M.; Ciaccio, M.F.; Rassbach, B.; Wollmann, R.; Mastrianni, J.A. 2007: Cytosolic prion protein toxicity is independent of cellular prion protein expression and prion propagation Journal of Virology 81(6): 2831-2837
Nicot, S.; Baron, T.G.M. 2010: Strain-specific proteolytic processing of the prion protein in prion diseases of ruminants transmitted in ovine transgenic mice Journal of General Virology 91(Part 2): 570-574
Montrasio, F.; Cozzio, A.; Flechsig, E.; Rossi, D.; Klein, M.A.; Rülicke, T.; Raeber, A.J.; Vosshenrich, C.A.; Proft, J.; Aguzzi, A.; Weissmann, C. 2001: B lymphocyte-restricted expression of prion protein does not enable prion replication in prion protein knockout mice Proceedings of the National Academy of Sciences of the United States of America 98(7): 4034-4037
Asante, E.A.; Linehan, J.M.; Desbruslais, M.; Joiner, S.; Gowland, I.; Wood, A.L.; Welch, J.; Hill, A.F.; Lloyd, S.E.; Wadsworth, J.D.F.; Collinge, J. 2002: BSE prions propagate as either variant CJD-like or sporadic CJD-like prion strains in transgenic mice expressing human prion protein EMBO Journal 21(23): 6358-6366
Wickner, R.B.; Edskes, H.K.; Son, M.; Wu, S. 2022: Anti-Prion Systems Block Prion Transmission, Attenuate Prion Generation, Cure Most Prions as they Arise and Limit Prion-Induced Pathology in Saccharomyces cerevisiae Biology 11(9)
Arsac, J.-N.ël.; Bétemps, D.; Morignat, E.; Féraudet, C.éc.; Bencsik, A.; Aubert, D.; Grassi, J.; Baron, T. 2009: Transmissibility of atypical scrapie in ovine transgenic mice: major effects of host prion protein expression and donor prion genotype Plos one 4(10): E7300
Espinosa, J.Carlos.; Comoy, E.E.; Marin-Moreno, A.; Aguilar-Calvo, P.; Birling, M-Christine.; Pitarch, Jé.Luis.; Deslys, J-Philippe.; Torres, J.María. 2019: Transgenic mouse models expressing human and macaque prion protein exhibit similar prion susceptibility on a strain-dependent manner Scientific Reports 9(1): 15699
Gu, Y.; Verghese, S.; Mishra, R.S.; Xu, X.; Shi, Y.; Singh, N. 2003: Mutant prion protein-mediated aggregation of normal prion protein in the endoplasmic reticulum: implications for prion propagation and neurotoxicity Journal of Neurochemistry 84(1): 10-22
Pan, T.; Li, R.; Kang, S.-C.; Pastore, M.; Wong, B.-S.; Ironside, J.; Gambetti, P.; Sy, M.-S. 2005: Biochemical fingerprints of prion diseases: scrapie prion protein in human prion diseases that share prion genotype and type Journal of Neurochemistry 92(1): 132-142
Krasemann, S.; Neumann, M.; Szalay, B.; Stocking, C.; Glatzel, M. 2013: Protease-sensitive prion species in neoplastic spleens of prion-infected mice with uncoupling of PrP(Sc) and prion infectivity Journal of General Virology 94(Part 2): 453-463
Cappai, R.; Stewart, L.; Jobling, M.F.; Thyer, J.M.; White, A.R.; Beyreuther, K.; Collins, S.J.; Masters, C.L.; Barrow, C.J. 1999: Familial prion disease mutation alters the secondary structure of recombinant mouse prion protein: implications for the mechanism of prion formation Biochemistry 38(11): 3280-3284
Sakurai-Yamashita, Y.; Sakaguchi, S.; Yoshikawa, D.; Okimura, N.; Masuda, Y.; Katamine, S.; Niwa, M. 2005: Female-specific neuroprotection against transient brain ischemia observed in mice devoid of prion protein is abolished by ectopic expression of prion protein-like protein Neuroscience 136(1): 281-287
Shkundina, I.S.; Kushnirov, V.V.; Tuite, M.F.; Ter-Avanesyan, M.D. 2006: The role of the N-terminal oligopeptide repeats of the yeast Sup35 prion protein in propagation and transmission of prion variants Genetics 172(2): 827-835