Amino acid sequence of the Felis catus prion protein

Gene

Volumn 341, Issue 1-2, 2004, Pages 249-253

  Lysek, Dominikus A ^a   Nivon, Lucas G ^a   Wüthrich, Kurt ^a  

^a ETH ZURICH   (Switzerland)

Author keywords

BSE infection; Prnp gene sequence; Species barrier; TSE

Indexed keywords

PRION PROTEIN;

AMINO ACID SEQUENCE; AMINO ACID SUBSTITUTION; ARTICLE; CAT; DOG; GENETIC SUSCEPTIBILITY; MINK; NONHUMAN; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; SEQUENCE ANALYSIS;

AMINO ACID SEQUENCE; ANIMALS; BASE SEQUENCE; CATS; DNA; MOLECULAR SEQUENCE DATA; PRIONS; SEQUENCE ALIGNMENT; SEQUENCE ANALYSIS, DNA; SEQUENCE HOMOLOGY, AMINO ACID; SEQUENCE HOMOLOGY, NUCLEIC ACID;

BOVINAE; CANIS; CANIS FAMILIARIS; FELIDAE; FELIS; FELIS CATUS; FELIS SILVESTRIS; MUSTELA; MUSTELA PUTORIUS; MUSTELA VISON;

EID: 5044231382     PISSN: 03781119     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.gene.2004.07.002     Document Type: Article

References (27)

1. J.C. Bartz, D.I. McKenzie, R.A. Bessen, R.F. Marsh, and J.M. Aiken Transmissible mink encephalopathy species barrier effect between ferret and mink: PrP gene and protein analysis J. Gen. Virol. 75 1994 2947 2953
2. D.A. Benson, I. Karsch-Mizrachi, D.J. Lipman, J. Ostell, and D.L. Wheeler GenBank Nucleic Acids Res. 31 2003 23 27
3. M. Billeter, R. Riek, G. Wider, S. Hornemann, R. Glockshuber, and K. Wüthrich Prion protein NMR structure and species barrier for prion diseases Proc. Natl. Acad. Sci. U. S. A. 94 1997 7281 7285
4. D.C. Bolton, R.D. Rudelli, J.R. Currie, and P.E. Bendheim Copurification of Sp33-37 and scrapie agent from hamster brain prior to detectable histopathology and clinical disease J. Gen. Virol. 72 1991 2905 2913
5. D.R. Borchelt, M. Scott, A. Taraboulos, N. Stahl, and S.B. Prusiner Scrapie and cellular prion proteins differ in their kinetics of synthesis and topology in cultured cells J. Cell Biol. 110 1990 743 752
6. J. Collinge Prion diseases of humans and animals: their causes and molecular basis Annu. Rev. Neurosci. 24 2001 519 550
7. T.L. James, H. Liu, N.B. Ulyanov, S. Farr-Jones, H. Zhang, D.G. Donne, K. Kaneko, D. Groth, I. Mehlhorn, S.B. Prusiner, and F.E. Cohen Solution structure of a 142-residue recombinant prion protein corresponding to the infectious fragment of the scrapie isoform Proc. Natl. Acad. Sci. U. S. A. 94 1997 10086 10091
8. Z.F. Kanyo, K.M. Pan, R.A. Williamson, D.R. Burton, S.B. Prusiner, R.J. Fletterick, and F.E. Cohen Antibody binding defines a structure for an epitope that participates in the PrPC→PrPSc conformational change J. Mol. Biol. 293 1999 855 863
9. J.K. Kirkwood, and A.A. Cunningham Epidemiological observations on spongiform encephalopathies in captive wild animals in the British Isles Vet. Rec. 135 1994 296 303
10. F. Ĺpez Garcia, R. Zahn, R. Riek, and K. Wüthrich NMR structure of the bovine prion protein Proc. Natl. Acad. Sci. U. S. A. 97 2000 8334 8339
11. B. Oesch, D. Westaway, M. Walchli, M.P. McKinley, S.B. Kent, R. Aebersold, R.A. Barry, P. Tempst, D.B. Teplow, and L.E. Hood A cellular gene encodes scrapie PrP 27-30 protein Cell 40 1985 735 746
12. S.B. Prusiner Prions Proc. Natl. Acad. Sci. U. S. A. 95 1998 13363 13383
13. R. Riek, S. Hornemann, G. Wider, M. Billeter, R. Glockshuber, and K. Ẅthrich NMR structure of the mouse prion protein domain PrP(121-321) Nature 382 1996 180 182
14. E. Rivera-Milla, C.A. Stuermer, and E. Malaga-Trillo An evolutionary basis for scrapie disease: identification of a fish prion mRNA Trends Genet. 19 2003 72 75
15. M. Rogers, F. Yehiely, M. Scott, and S.B. Prusiner Conversion of truncated and elongated prion proteins into the scrapie isoform in cultured cells Proc. Natl. Acad. Sci. U. S. A. 90 1993 3182 3186
16. S.J. Ryder, G.A. Wells, J.M. Bradshaw, and G.R. Pearson Inconsistent detection of PrP in extraneural tissues of cats with feline spongiform encephalopathy Vet. Rec. 148 2001 437 441
17. H.M. Schützl, M. Da Costa, L. Taylor, F.E. Cohen, and S.B. Prusiner Prion protein gene variation among primates J. Mol. Biol. 245 1995 362 374
18. M. Scott, D. Groth, D. Foster, M. Torchia, S.L. Yang, S.J. DeArmond, and S.B. Prusiner Propagation of prions with artificial properties in transgenic mice expressing chimeric PrP genes Cell 73 1993 979 988
19. T. Simonic, S. Duga, B. Strumbo, R. Asselta, F. Ceciliani, and S. Ronchi cDNA cloning of turtle prion protein FEBS Lett. 469 2000 33 38
20. B. Strumbo, S. Ronchi, L.C. Bolis, and T. Simonic Molecular cloning of the cDNA coding for Xenopus laevis prion protein FEBS Lett. 508 2001 170 174
21. T. Van Rheede, M.M. Smolenaars, O. Madsen, and W.W. De Jong Molecular evolution of the Mammalian prion protein Mol. Biol. Evol. 20 2003 111 121
22. I. Vorberg, M.H. Groschup, E. Pfaff, and S.A. Priola Multiple amino acid residues within the rabbit prion protein inhibit formation of its abnormal isoform J. Virol. 77 2003 2003 2009
23. C. Weissmann Molecular biology of transmissible spongiform encephalopathies FEBS Lett. 389 1996 3 11
24. C. Weissmann, M. Enari, P.C. Klohn, D. Rossi, and E. Flechsig Transmission of prions Proc Natl. Acad. Sci. U. S. A. 99 2002 16378 16783
25. H. Wille, M.D. Michelitsch, V. Guenebaut, S. Supattapone, A. Serban, F.E. Cohen, D.A. Agard, and S.B. Prusiner Structural studies of the scrapie prion protein by electron crystallography Proc. Natl. Acad. Sci. U. S. A. 99 2002 3563 3568
26. F. Wopfner, G. Weidenhofer, R. Schneider, A. von Brunn, S. Gilch, T.F. Schwarz, T. Werner, and H.M. Scḧtzl Analysis of 27 mammalian and 9 avian PrPs reveals high conservation of flexible regions of the prion protein J. Mol. Biol. 289 1999 1163 1168
27. R. Zahn, A. Liu, T. Lührs, R. Riek, C. von Schroetter, F. Ĺpez Garcia, M. Billeter, L. Calzolai, G. Wider, and K. Wüthrich NMR solution structure of the human prion protein Proc. Natl. Acad. Sci. U. S. A. 97 2000 145 150