Familial transmission of the FMR1 CGG repeat.

Journal Article (Journal Article)

To better define the nature of FMR1 CGG-repeat expansions, changes in allele sizes for 191 families with fragile X and for 33 families with gray-zone repeats (40-60) were analyzed. Expansion of the fragile X chromosome to the full mutation was seen in 13.4% of offspring from premutation mothers with 56-59 repeats, 20.6% of those with 60-69 repeats, 57.8% of those with 70-79 repeats, 72.9% of those with 80-89 repeats, and 97.3% of those with 90-199 repeats. For premutation fathers, the majority (62%) of their daughters had a larger repeat number, while a few had either a smaller (22%) or the same (16%) repeat number, compared with their fathers' sizes. However, daughters with a smaller repeat number were observed only if their fathers had > or = 80 repeats. Fifteen (39.5%) of 38 such daughters carried a smaller repeat than did their fathers. We observed that a similar repeat number was inherited more often than expected by chance, among the members of a sibship segregating fragile X. This familial clustering, observed in the offspring of both males and females with a premutation, implies there may be an additional factor, independent of parental repeat size, that influences CGG-repeat instability. Instability in gray-zone allele transmissions was observed in 25% of alleles with 50-60 CGGs but in <8% of those with 40-49 CGGs. Examination of gray-zone allele organization revealed that long tracts of pure CGGs (>34) are not always unstably transmitted. These results raise new questions regarding the familial factors that may determine transmission expansions.

Full Text

Duke Authors

Cited Authors

  • Nolin, SL; Lewis, FA; Ye, LL; Houck, GE; Glicksman, AE; Limprasert, P; Li, SY; Zhong, N; Ashley, AE; Feingold, E; Sherman, SL; Brown, WT

Published Date

  • December 1996

Published In

Volume / Issue

  • 59 / 6

Start / End Page

  • 1252 - 1261

PubMed ID

  • 8940270

Pubmed Central ID

  • PMC1914886

International Standard Serial Number (ISSN)

  • 0002-9297


  • eng

Conference Location

  • United States