Study of three intragenic polymorphisms in the Machado-Joseph disease gene (MJD1) in relation to genetic instability of the (CAG)(n) tract

• Type: Article in International Scientific Journal
• Date: 1999

Authors

Maciel, P (Author) Other; Gasper, C (Author) Other; Guimaraes, L (Author) Other; Goto, J (Author) Other; Lopez Cendes, I (Author) Other; Hayes, S (Author) Other; Arvidsson, K (Author) Other; Dias, A (Author) Other; Sequeiros, J (Author) Other; Alda Sousa (Author) ICBAS; Rouleau, GA (Author) Other

Journal

Title: European Journal of Human Genetics

Vol. 7

Pages: 147-156

ISSN: 1018-4813

Publisher: Springer Nature

Indexing

ISI Web of Knowledge - 14 Citations

Scopus - 18 Citations

Other information

Authenticus ID: P-001-55G

DOI: 10.1038/sj.ejhg.5200264

Abstract (EN): Intergenerational instability is one of the most important features of the disease-associated trinucleotide expansions, leading to variation in size of the repeat among and,within families, which manifests as variable age at onset and severity, and is probably the basis for the occurrence of anticipation. Several factors are known to affect the degree of instability, namely the type of repeated sequence, its initial size, the presence or absence of interruptions in the repetitive tract and the gender of the transmitting parent. A recent study demonstrated the effect of an intragenic polymorphism (C(987)GG/G(987)GG) in the Machado-Joseph disease causative gene, immediately downstream of the CAG repeat, on the intergenerational instability of the expanded repeat. Surprisingly, there was an effect not only of the specific allele in cis to the disease chromosome, but also of the allele on the normal chromosome, suggesting the existence of an interaction between the normal and expanded alleles that affects the fidelity of replication of the (CAG)(n) tract. This effect could be a direct effect of the polymorphism studied or, alternatively, this polymorphism could be in disequilibrium with some other flanking sequence which affects the instability of the repetitive (CAG)(n) tract. In order to confirm the previous results in a different population and to distinguish between a direct and indirect effect of the CGG/GGG polymorphism, we typed 70 parent-progeny pairs for which the variation in the (CAG)(n) length in the MJD1 gene was known, for three intragenic polymorphisms: C(987)GG/G(987)GG and two additional, newly described ones, TA (A) under bar(1118)/TA (C) under bar(1118) and (A) under bar(669)TG/(G) under bar(669)TG. We also typed a control population of 125 individuals for the (A) under bar(669)TG/(G) under bar(669)TG, (C) under bar(987)GG/(G) under bar(987)GG and TA (A) under bar(1118)/TA (C) under bar(1118) polymorphisms, in an attempt to identify any association between haplotype and (CAG)(n) length in normal chromosomes, suggestive of an instability-predisposing effect of the repeat-flanking sequences, which could have led to the origin of the MJD mutation in the human population. We confirmed the effect of the (C) under bar(987)GG/(G) under bar(987)GG polymorphism on intergenerational instability when present in trans, Our results suggest that this effect is restricted to a small region of the gene, immediately downstream of the CAG repeat, which includes this particular nucleotide substitution and the stop codon of the MJD1 cDNA, and is not a more widespread chromosomal effect, The lack of a significant association of any specific intragenic haplotype with larger CAG repeats in normal chromosomes, together with the absence of an effect of the intragenic haplotype in cis on the intergenerational instability of the expanded (CAG)(n) in MJD families does not indicate the existence of an instability-predisposing haplotype.

Language: English

Type (Professor's evaluation): Scientific

No. of pages: 10