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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

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单位: [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]CHINA JAPAN FRIENDSHIP HOSP,DEPT NEUROL,BEIJING 100029,PEOPLES R CHINA [8]UNIV SAO PAULO,HOSP & CLIN,DEPT NEUROL,BR-05508 SAO PAULO,BRAZIL [9]HOP SPECIALITES,SERV NEUROL,RABAT,MOROCCO [10]CHU BORDEAUX,SERV NEUROL,PESSAC,FRANCE [11]GENETHON,F-91000 EVRY,FRANCE [12]INST PASTEUR,CNRS URA 1445,UNITE GENET MOL HUMAN,F-75724 PARIS,FRANCE [13]JICHI MED SCH,DEPT NEUROL,MINAMI KAWACHI,TOCHIGI 32904,JAPAN
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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.

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大类 | 2 区 生物学
小类 | 3 区 生化与分子生物学 3 区 遗传学
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出版当年[1994]版:
最新[2023]版:
Q2 GENETICS & HEREDITY Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY

影响因子: 最新[2023版] 最新五年平均[2021-2025] 出版当年[1994版] 出版当年五年平均[1990-1994] 出版前一年[1993版]

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