Machado-Joseph disease gene products carrying different carboxyl termini

被引:64
作者
Goto, J
Watanabe, M
Ichikawa, Y
Yee, SB
Ihara, N
Endo, K
Igarashi, S
Takiyama, Y
Gaspar, C
Maciel, P
Tsuji, S
Rouleau, GA
Kanazawa, I
机构
[1] UNIV TOKYO,GRAD SCH SCI,DEPT BIOL SCI,DIV ANTHROPOL,BUNKYO KU,TOKYO 113,JAPAN
[2] NIIGATA UNIV,BRAIN RES INST,DEPT NEUROL,NIIGATA 951,JAPAN
[3] JICHI MED SCH,DEPT NEUROL,MINAMI KAWACHI,TOCHIGI 32904,JAPAN
[4] MCGILL UNIV,MONTREAL GEN HOSP,DEPT NEUROL,RES INST,MONTREAL,PQ H3G 1A4,CANADA
[5] MCGILL UNIV,CTR RES NEUROSCI,MONTREAL,PQ H3G 1A4,CANADA
基金
日本科学技术振兴机构;
关键词
Machado-Joseph disease; cDNA; stop codon; polymorphism; linkage disequilibrium; spinocerebellar ataxia;
D O I
10.1016/S0168-0102(97)00056-4
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Three cDNA clones for the Machado-Joseph disease gene (MJD1) were isolated, two of which have a new exon sequence and a distinct 3' terminal nucleotide sequence resulting in a new carboxyl terminal domain in the translated product. The nucleotide sequence of the other one is similar to the previously published one except for five polymorphisms, one of which is a single nucleotide substitution resulting in a change from the stop codon (TAA; allele A) to a tyrosine residue (TAC; allele C). Genetic analysis results suggest that Japanese MJD mutations are associated with allele A. (C) 1997 Elsevier Science Ireland Ltd.
引用
收藏
页码:373 / 377
页数:5
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