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Expansion of the Fragile X CGG Repeat in Females with Premutation or Intermediate Alleles

By Sarah L. Nolin, W. Ted Brown, Anne Glicksman, George E. Jr. Houck, Alice D. Gargano, Amy Sullivan, Valérie Biancalana, Karen Bröndum-Nielsen, Helle Hjalgrim, Elke Holinski-Feder, Frank Kooy, John Longshore, James Macpherson, Jean-Louis Mandel, Gert Matthijs, Francois Rousseau, Peter Steinbach, Marja-Leena Väisänen, Harriet von Koskull and Stephanie L. Sherman

Abstract

The CGG repeat in the 5′ untranslated region of the fragile X mental retardation 1 gene (FMR1) exhibits remarkable instability upon transmission from mothers with premutation alleles. A collaboration of 13 laboratories in eight countries was established to examine four issues concerning FMR1 CGG-repeat instability among females with premutation (∼55–200 repeats) and intermediate (∼46–60 repeats) alleles. Our central findings were as follows: (1) The smallest premutation alleles that expanded to a full mutation (>200 repeats) in one generation contained 59 repeats; sequence analysis of the 59-repeat alleles from these two females revealed no AGG interruptions within the FMR1 CGG repeat. (2) When we corrected for ascertainment and recalculated the risks of expansion to a full mutation, we found that the risks for premutation alleles with <100 repeats were lower than those previously published. (3) When we examined the possible influence of sex of offspring on transmission of a full mutation—by analysis of 567 prenatal fragile X studies of 448 mothers with premutation and full-mutation alleles—we found no significant differences in the proportion of full-mutation alleles in male or female fetuses. (4) When we examined 136 transmissions of intermediate alleles from 92 mothers with no family history of fragile X, we found that, in contrast to the instability observed in families with fragile X, most (99/136 [72.8%]) transmissions of intermediate alleles were stable. The unstable transmissions (37/136 [27.2%]) in these families included both expansions and contractions in repeat size. The instability increased with the larger intermediate alleles (19% for 49–54 repeats, 30.9% for 55–59, and 80% for 60–65 repeats). These studies should allow improved risk assessments for genetic counseling of women with premutation or intermediate-size alleles

Topics: Articles
Publisher: The American Society of Human Genetics
Year: 2003
OAI identifier: oai:pubmedcentral.nih.gov:379237
Provided by: PubMed Central
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