The Role of Size, Sequence and Haplotype in the Stability of FRAXA and FRAXE Alleles during Transmission
Open Access
- 1 February 1997
- journal article
- research article
- Published by Oxford University Press (OUP) in Human Molecular Genetics
- Vol. 6 (2) , 173-184
- https://doi.org/10.1093/hmg/6.2.173
Abstract
Factors involved in the stability of trinucleotide repeats during transmission were studied in 139 families in which a full mutation, premutation or intermediate allele at either FRAXA or FRAXE was segregating. The transmission of alleles at FRAXA, FRAXE and four microsatellite loci were recorded for all individuals. Instability within the minimal and common ranges (0–40 repeats for FRAXA, 0–30 repeats for FRAXE) was extremely rare; only one example was observed, an increase in size at FRAXA from 29 to 39 repeats. Four FRAXA and three FRAXE alleles in the intermediate range (41–60 repeats for FRAXA, 31–60 repeats for FRAXE) were unstably transmitted. Instability was more frequent for FRAXA intermediate alleles that had a tract of pure CGG greater than 37 although instability only occurred in two of 13 such transmissions: the changes observed were limited to only one or two repeats. Premutation FRAXA alleles over 100 repeats expanded to a full mutation during female transmission in 100% of cases, in agreement with other published series. There was no clear correlation between haplotype and probability of expansion of FRAXA premutations. Instability at FRAXA or FRAXE was more often observed in conjunction with a second instability at an independent locus suggesting general genomic instability as a possible mechanism by which at least some FRAXA and FRAXE mutations arise.Keywords
This publication has 41 references indexed in Scilit:
- Identification of FMR2, a novel gene associated with the FRAXE CCG repeat and CpG islandNature Genetics, 1996
- Identification of the gene FMR2, associated with FRAXE mental retardationNature Genetics, 1996
- Contribution of the FMR1 gene mutation to human intellectual dysfunctionNature Genetics, 1995
- Unusual (CGG)n expansion and recombination in a family with fragile X and DiGeorge syndrome.Journal of Medical Genetics, 1995
- Hotspot for deletions in the CGG repeat region of FMR1 in fragile X patientsHuman Molecular Genetics, 1995
- Trinucleotide repeat amplification and hypermethylation of a CpG island in FRAXE mental retardationCell, 1993
- A point mutation in the FMR-1 gene associated with fragile X mental retardationNature Genetics, 1993
- Mapping of DNA Instability at the Fragile X to a Trinucleotide Repeat Sequence P(CCG) nScience, 1991
- Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndromePublished by Elsevier ,1991
- Instability of a 550-Base Pair DNA Segment and Abnormal Methylation in Fragile X SyndromeScience, 1991