Prion protein genes and prion diseases: studies in transgenic mice

被引:24
|
作者
Telling, GC
机构
[1] Univ Kentucky, Dept Microbiol & Immunol, Sanders Brown Ctr Aging, Lexington, KY 40536 USA
[2] Univ Kentucky, Dept Neurol, Lexington, KY 40536 USA
关键词
prions; transgenic mice;
D O I
10.1046/j.1365-2990.2000.00253.x
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
In the past decade, manipulation of PrP genes by transgenesis in mice has provided important insights into mechanisms of prion propagation and the molecular basis of prion strains and species barriers. Despite these advances, our understanding of these unique pathogens is far from complete. This review focuses on PrP gene knockout and gene replacement studies, PrP structure and function, and transgenic models of human and animal prion diseases. Transgenic approaches will doubtless remain the cornerstone of investigations into the prion diseases in the coming years, which will include mechanistic studies of prion pathogenesis and prion transmission barriers. Transgenic models will also be important tools for the evaluation of potential therapeutic agents for prion diseases.
引用
收藏
页码:209 / 220
页数:12
相关论文
共 50 条
  • [1] Transgenic and knockout mice in research on prion diseases
    Raeber, AJ
    Brandner, S
    Klein, MA
    Benninger, Y
    Musahl, C
    Frigg, R
    Roeckl, C
    Fischer, MB
    Weissmann, C
    Aguzzi, A
    BRAIN PATHOLOGY, 1998, 8 (04) : 715 - 733
  • [2] Strain-specific proteolytic processing of the prion protein in prion diseases of ruminants transmitted in ovine transgenic mice
    Nicot, Simon
    Baron, Thierry G. M.
    JOURNAL OF GENERAL VIROLOGY, 2010, 91 : 570 - 574
  • [3] Inducible expression of the prion protein in transgenic mice
    Si-Hoe, SL
    Adles, C
    Harris, D
    NEUROBIOLOGY OF AGING, 2002, 23 (01) : S66 - S66
  • [4] TRANSGENIC ANIMALS AND PRION DISEASES
    ONEIL, BD
    NEW ZEALAND VETERINARY JOURNAL, 1995, 43 (02) : 88 - 88
  • [5] Transgenic analysis of prion diseases
    Moore, RC
    Melton, DW
    MOLECULAR HUMAN REPRODUCTION, 1997, 3 (06) : 529 - 544
  • [6] GENETICS OF PRION DISEASES AND PRION DIVERSITY IN MICE
    CARLSON, GA
    DEARMOND, SJ
    TORCHIA, M
    WESTAWAY, D
    PRUSINER, SB
    PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES, 1994, 343 (1306) : 363 - 369
  • [7] N-terminally tagged prion protein supports prion propagation in transgenic mice
    Telling, GC
    Tremblay, P
    Torchia, M
    Dearmond, SJ
    Cohen, FE
    Prusiner, SB
    PROTEIN SCIENCE, 1997, 6 (04) : 825 - 833
  • [8] N-terminally tagged prion protein supports prion propagation in transgenic mice
    Telling, GC
    Tremblay, P
    Torchia, M
    DeArmond, SJ
    Cohen, FE
    Prusiner, SB
    MOLECULAR BIOLOGY OF THE CELL, 1996, 7 : 3788 - 3788
  • [9] SPONTANEOUS NEURODEGENERATION IN TRANSGENIC MICE WITH MUTANT PRION PROTEIN
    HSIAO, KK
    SCOTT, M
    FOSTER, D
    GROTH, DF
    DEARMOND, SJ
    PRUSINER, SB
    SCIENCE, 1990, 250 (4987) : 1587 - 1590
  • [10] Conformational conversion of prion protein in prion diseases
    Zhou, Zheng
    Xiao, Gengfu
    ACTA BIOCHIMICA ET BIOPHYSICA SINICA, 2013, 45 (06) : 465 - 476