Intergenerational instability of the CAG repeat of the gene for Machado-Joseph disease (MJD1) is affected by the genotype of the normal chromosome: Implications for the molecular mechanisms of the instability of the CAG repeat

被引:74
作者
Igarashi, S
Takiyama, Y
Cancel, G
Rogaeva, EA
Sasaki, H
Wakisaka, A
Zhou, YX
Takano, H
Endo, K
Sanpei, K
Oyake, M
Tanaka, H
Stevanin, G
Abbas, N
Durr, A
Rogaev, EI
Sherrington, R
Tsuda, T
Ikeda, M
Cassa, E
Nishizawa, M
Benomar, A
Julien, J
Weissenbach, J
Wang, GX
Agid, Y
StGeorgeHyslop, PH
Brice, A
Tsuji, S
机构
[1] NIIGATA UNIV,BRAIN RES INST,DEPT NEUROL,NIIGATA 951,JAPAN
[2] HOP LA PITIE SALPETRIERE,INSERM U289,PARIS,FRANCE
[3] HOP LA PITIE SALPETRIERE,FEDERAT NEUROL,PARIS,FRANCE
[4] UNIV TORONTO,CTR RES NEURODEGENERAT DIS,TORONTO,ON,CANADA
[5] TORONTO HOSP,DIV NEUROL,DEPT MED,TORONTO,ON M5S 1A8,CANADA
[6] HOKKAIDO UNIV,SCH MED,DEPT NEUROL,SAPPORO,HOKKAIDO 060,JAPAN
[7] HOKKAIDO UNIV,SCH MED,DEPT NEUROL,SAPPORO,HOKKAIDO 060,JAPAN
[8] CHINA JAPAN FRIENDSHIP HOSP,DEPT NEUROL,BEIJING 100029,PEOPLES R CHINA
[9] UNIV SAO PAULO,HOSP & CLIN,DEPT NEUROL,BR-05508 SAO PAULO,BRAZIL
[10] HOP SPECIALITES,SERV NEUROL,RABAT,MOROCCO
[11] CHU BORDEAUX,SERV NEUROL,PESSAC,FRANCE
[12] GENETHON,F-91000 EVRY,FRANCE
[13] INST PASTEUR,CNRS URA 1445,UNITE GENET MOL HUMAN,F-75724 PARIS,FRANCE
[14] JICHI MED SCH,DEPT NEUROL,MINAMI KAWACHI,TOCHIGI 32904,JAPAN
关键词
D O I
10.1093/hmg/5.7.923
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Machado-Joseph disease (MJD) is an autosomal dominant neurodegenerative disorder caused by unstable expansion of a CAG repeat in the MJD1 gene at 14q32.1. To identify elements affecting the intergenerational instability of the CAG repeat, we investigated whether the CGG/GGG polymorphism at the 3' end of the CAG repeat affects intergenerational instability of the CAG repeat The [expanded (CAG)n-CGG]/[normal (CAG)n-GGG] haplotypes were found to result in significantly greater instability of the CAG repeat compared to the [expanded (CAG)n-CGG]/[normal (CAG)n-CGG] or [expanded (CAG)nGGG]/[normal (CAG)n-GGG] haplotypes. Multiple stepwise logistic regression analysis revealed that the relative risk for a large intergenerational change in the number of CAG repeat units (<-2 or >2) is 7.7-fold (95% CI: 2.5-23.9) higher in the case of paternal transmission than in that of maternal transmission and 7.4-fold (95% CI: 2.4-23.3) higher in the case of transmission from a parent with the [expanded (CAG)n-CGG]/[normal (CAG)n-GGG] haplotypes than in that of transmission from a parent with the [expanded (CAG)n-CGG]/[normal (CAG)n-CGG] or [expanded (CAG)n-GGG]/[normal (CAG)n-GGG] haplotypes. The combination of paternal transmission and the [expanded (CAG)n-CGG]/[normal (CAG)n-GGG] haplotypes resulted in a 75.2-fold (95% CI: 9.0-625.0) increase in the relative risk compared with that of maternal transmission and the [expanded (CAG)n-CGG]/[normal (CAG)n-CGG] or [expanded (CAG)n-GGG]/[normal (CAG)n-GGG] haplotypes. The results suggest that an inter-allelic interaction is involved in the intergenerational instability of the expanded CAG repeat.
引用
收藏
页码:923 / 932
页数:10
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