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Prevalence of carriers of premutation-size alleles of the FMRI gene--and implications for the population genetics of the fragile X syndrome.

Publication Type:

Journal Article

Source:

Am J Hum Genet, Volume 57, Issue 5, p.1006-18 (1995)

Keywords:

Alleles, Base Sequence, Female, Fragile X Mental Retardation Protein, Fragile X Syndrome, France, Genetic Linkage, Genetic Testing, Genetics, Population, Heterozygote, Humans, Molecular Sequence Data, Nerve Tissue Proteins, Prevalence, Quebec, Repetitive Sequences, Nucleic Acid, RNA-Binding Proteins

Abstract:

<p>The fragile X syndrome is the second leading cause of mental retardation after Down syndrome. Fragile X premutations are not associated with any clinical phenotype but are at high risk of expanding to full mutations causing the disease when they are transmitted by a carrier woman. There is no reliable estimate of the prevalence of women who are carriers of fragile X premutations. We have screened 10,624 unselected women by Southern blot for the presence of FMR1 premutation alleles and have confirmed their size by PCR analysis. We found 41 carriers of alleles with 55-101 CGG repeats, a prevalence of 1/259 women (95% confidence interval 1/373-1/198). Thirty percent of these alleles carry an inferred haplotype that corresponds to the most frequent haplotype found in fragile X males and may indeed constitute premutations associated with a significant risk of expansion on transmission by carrier women. We identified another inferred haplotype that is rare in both normal and fragile X chromosomes but that is present on 13 (57%) of 23 chromosomes carrying FMR1 alleles with 53-64 CGG repeats. This suggests either (1) that this haplotype may be stable or (2) that the associated premutation-size alleles have not yet reached equilibrium in this population and that the incidence of fragile X syndrome may increase in the future.</p>

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