Kennedy disease

被引:111
作者
Fischbeck, KH
机构
关键词
D O I
10.1023/A:1005344403603
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Kennedy disease is a disorder with progressive motor neuron degeneration that is caused by trinucleotide repeat expansion in the androgen receptor gene. The disease mechanism likely involves toxicity of an expanded polyglutamine tract in the androgen receptor protein. This mechanism is probably shared by other neurodegenerative disorders with polyglutamine expansion, including Huntington disease. Attempts at reproducing the Kennedy disease phenotype by introducing the expanded androgen receptor into cultured neuronal cells and transgenic animals have thus far been unsuccessful, but recently developed model systems with other expanded polyglutamine constructs should allow the pathogenesis of these diseases to be elucidated.
引用
收藏
页码:152 / 158
页数:7
相关论文
共 21 条
[1]   STABILITY OF AN EXPANDED TRINUCLEOTIDE REPEAT IN THE ANDROGEN RECEPTOR GENE IN TRANSGENIC MICE [J].
BINGHAM, PM ;
SCOTT, MO ;
WANG, SP ;
MCPHAUL, MJ ;
WILSON, EM ;
GARBERN, JY ;
MERRY, DE ;
FISCHBECK, KH .
NATURE GENETICS, 1995, 9 (02) :191-196
[2]  
BROOKS BP, 1997, IN PRESS NEUROBIOL D
[3]   SCA1 TRANSGENIC MICE - A MODEL FOR NEURODEGENERATION CAUSED BY AN EXPANDED CAG TRINUCLEOTIDE REPEAT [J].
BURRIGHT, EN ;
CLARK, HB ;
SERVADIO, A ;
MATILLA, T ;
FEDDERSEN, RM ;
YUNIS, WS ;
DUVICK, LA ;
ZOGHBI, HY ;
ORR, HT .
CELL, 1995, 82 (06) :937-948
[4]   Reduced androgen receptor gene expression with first exon CAG repeat expansion [J].
Choong, CS ;
Kemppainen, JA ;
Zhou, ZX ;
Wilson, EM .
MOLECULAR ENDOCRINOLOGY, 1996, 10 (12) :1527-1535
[5]   GENETIC-VARIATION AT 5 TRIMERIC AND TETRAMERIC TANDEM REPEAT LOCI IN 4 HUMAN-POPULATION GROUPS [J].
EDWARDS, A ;
HAMMOND, HA ;
JIN, L ;
CASKEY, CT ;
CHAKRABORTY, R .
GENOMICS, 1992, 12 (02) :241-253
[6]  
FISCHBECK KH, 1991, ADV NEUROL, V56, P209
[7]   LOCALIZATION OF THE GENE FOR X-LINKED SPINAL MUSCULAR-ATROPHY [J].
FISCHBECK, KH ;
IONASESCU, V ;
RITTER, AW ;
IONASESCU, R ;
DAVIES, K ;
BALL, S ;
BOSCH, P ;
BURNS, T ;
HAUSMANOWAPETRUSEWICZ, I ;
BORKOWSKA, J ;
RINGEL, SP ;
STERN, LZ .
NEUROLOGY, 1986, 36 (12) :1595-1598
[8]   X-LINKED RECESSIVE BULBOSPINAL NEURONOPATHY - A REPORT OF 10 CASES [J].
HARDING, AE ;
THOMAS, PK ;
BARAITSER, M ;
BRADBURY, PG ;
MORGANHUGHES, JA ;
PONSFORD, JR .
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 1982, 45 (11) :1012-1019
[9]   Expanded polyglutamine in the Machado-Joseph disease protein induces cell death in vitro and in vivo [J].
Ikeda, H ;
Yamaguchi, M ;
Sugai, S ;
Aze, Y ;
Narumiya, S ;
Kakizuka, A .
NATURE GENETICS, 1996, 13 (02) :196-202
[10]   CAG EXPANSIONS IN A NOVEL GENE FOR MACHADO-JOSEPH DISEASE AT CHROMOSOME 14Q32.1 [J].
KAWAGUCHI, Y ;
OKAMOTO, T ;
TANIWAKI, M ;
AIZAWA, M ;
INOUE, M ;
KATAYAMA, S ;
KAWAKAMI, H ;
NAKAMURA, S ;
NISHIMURA, M ;
AKIGUCHI, I ;
KIMURA, J ;
NARUMIYA, S ;
KAKIZUKA, A .
NATURE GENETICS, 1994, 8 (03) :221-228