Studies of the CAG repeat in the Machado-Joseph disease gene in Taiwan

被引:18
作者
Hsieh, ML
Tsai, HF
Lu, TM
Yang, CY
Wu, HM
Li, SY
机构
[1] CHUNG SHAN MED & DENT COLL,CYTOGENET LAB,TAICHUNG,TAIWAN
[2] CHUNG SHAN MED & DENT COLL,INST MED,TAICHUNG,TAIWAN
[3] CHUNG SHAN MED & DENT COLL HOSP,DEPT NEUROL,TAICHUNG,TAIWAN
[4] KUANG TIEN GEN HOSP,DEPT NEUROL,TAICHUNG,TAIWAN
关键词
D O I
10.1007/s004390050483
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Machado-Joseph disease (MJD) is an autosomal dominant spinocerebellar degeneration characterized by cerebellar ataxia and pyramidal signs associated in varying degrees with a dystonic-rigid extrapyramidal syndrome or peripheral amyotrophy. Unstable CAG trinucleotide repeat expansion in the MJD gene on the long arm of chromosome 14 has been identified as the pathological mutation for MJD. While investigating the distribution of CAG repeat lengths of the MJD gene in Taiwan's population, we have identified 18 MJD-affected patients and 12 at-risk individuals in seven families. In addition, we have analyzed the range of CAG repeat lengths in 96 control individuals. The CAG repeat number ranged from 13 to 44 in the controls and 72-85 in the affected and at-risk individuals. Our results indicated that the CAG repeat number was inversely correlated with the age of onset. The differences in CAG repeat length between parent and child and between siblings are greater with paternal transmission than maternal transmission. Our data show a tendency towards the phenomenon of anticipation in the MJD families but do not support unidirectional expansion of CAG repeats during transmission. We also demonstrated that PCR amplification of the CAG repeats in the MJD gene from villous DNA was possible and might prove useful as a diagnostic tool for affected families in the future.
引用
收藏
页码:155 / 162
页数:8
相关论文
共 34 条
[1]   THE RELATIONSHIP BETWEEN TRINUCLEOTIDE (CAG) REPEAT LENGTH AND CLINICAL-FEATURES OF HUNTINGTONS-DISEASE [J].
ANDREW, SE ;
GOLDBERG, YP ;
KREMER, B ;
TELENIUS, H ;
THEILMANN, J ;
ADAM, S ;
STARR, E ;
SQUITIERI, F ;
LIN, BY ;
KALCHMAN, MA ;
GRAHAM, RK ;
HAYDEN, MR .
NATURE GENETICS, 1993, 4 (04) :398-403
[2]  
CANCEL G, 1995, AM J HUM GENET, V57, P809
[3]   GAMETIC AND SOMATIC TISSUE-SPECIFIC HETEROGENEITY OF THE EXPANDED SCA1 CAG REPEAT IN SPINOCEREBELLAR ATAXIA TYPE-1 [J].
CHONG, SS ;
MCCALL, AE ;
COTA, J ;
SUBRAMONY, SH ;
ORR, HT ;
HUGHES, MR ;
ZOGHBI, HY .
NATURE GENETICS, 1995, 10 (03) :344-350
[4]   EVIDENCE FOR A MECHANISM PREDISPOSING TO INTERGENERATIONAL CAG REPEAT INSTABILITY IN SPINOCEREBELLAR ATAXIA TYPE-I [J].
CHUNG, MY ;
RANUM, LPW ;
DUVICK, LA ;
SERVADIO, A ;
ZOGHBI, HY ;
ORR, HT .
NATURE GENETICS, 1993, 5 (03) :254-258
[5]   AUTOSOMAL DOMINANT SYSTEM DEGENERATION IN PORTUGUESE FAMILIES OF AZORES ISLANDS - NEW GENETIC DISORDER INVOLVING CEREBELLAR, PYRAMIDAL, EXTRAPYRAMIDAL AND SPINAL-CORD MOTOR FUNCTIONS [J].
COUTINHO, P ;
ANDRADE, C .
NEUROLOGY, 1978, 28 (07) :703-709
[6]  
COUTINHO P, 1977, MEDICO, V82, P446
[7]   TRINUCLEOTIDE REPEAT LENGTH INSTABILITY AND AGE-OF-ONSET IN HUNTINGTONS-DISEASE [J].
DUYAO, M ;
AMBROSE, C ;
MYERS, R ;
NOVELLETTO, A ;
PERSICHETTI, F ;
FRONTALI, M ;
FOLSTEIN, S ;
ROSS, C ;
FRANZ, M ;
ABBOTT, M ;
GRAY, J ;
CONNEALLY, P ;
YOUNG, A ;
PENNEY, J ;
HOLLINGSWORTH, Z ;
SHOULSON, I ;
LAZZARINI, A ;
FALEK, A ;
KOROSHETZ, W ;
SAX, D ;
BIRD, E ;
VONSATTEL, J ;
BONILLA, E ;
ALVIR, J ;
CONDE, JB ;
CHA, JH ;
DURE, L ;
GOMEZ, F ;
RAMOS, M ;
SANCHEZRAMOS, J ;
SNODGRASS, S ;
DEYOUNG, M ;
WEXLER, N ;
MOSCOWITZ, C ;
PENCHASZADEH, G ;
MACFARLANE, H ;
ANDERSON, M ;
JENKINS, B ;
SRINIDHI, J ;
BARNES, G ;
GUSELLA, J ;
MACDONALD, M .
NATURE GENETICS, 1993, 4 (04) :387-392
[8]   VARIATION OF THE CGG REPEAT AT THE FRAGILE-X SITE RESULTS IN GENETIC INSTABILITY - RESOLUTION OF THE SHERMAN PARADOX [J].
FU, YH ;
KUHL, DPA ;
PIZZUTI, A ;
PIERETTI, M ;
SUTCLIFFE, JS ;
RICHARDS, S ;
VERKERK, AJMH ;
HOLDEN, JJA ;
FENWICK, RG ;
WARREN, ST ;
OOSTRA, BA ;
NELSON, DL ;
CASKEY, CT .
CELL, 1991, 67 (06) :1047-1058
[9]  
*HUNT DIS COLL RES, 1993, CELL, V72, P971
[10]   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