Phenotypic characterization of individuals with 30-40 CAG repeats in the Huntington disease (HD) gene reveals HD cases with 36 repeats and apparently normal elderly individuals with 36-39 repeats.
- 1 July 1996
- journal article
- case report
- Vol. 59 (1) , 16-22
Abstract
Abnormal CAG expansions in the IT-15 gene are associated with Huntington disease (HD). In the diagnostic setting it is necessary to define the limits of the CAG size ranges on normal and HD-associated chromosomes. Most large analyses that defined the limits of the normal and pathological size ranges employed PCR assays, which included the CAG repeats and a CCG repeat tract that was thought to be invariant. Many of these experiments found an overlap between the normal and disease size ranges. Subsequent findings that the CCG repeats vary by 8 trinucleotide lengths suggested that the limits of the normal and disease size ranges should be reevaluated with assays that exclude the CCG polymorphism. Since patients with between 30 and 40 repeats are rare, a consortium was assembled to collect such individuals. All 178 samples were reanalyzed in Cambridge by using assays specific for the CAG repeats. We have optimized methods for reliable sizing of CAG repeats and show cases that demonstrate the dangers of using PCR assays that include both the CAG and CCG polymorphisms. Seven HD patients had 36 repeats, which confirms that this allele is associated with disease. Individuals without apparent symptoms or signs of HD were found at 36 repeats (aged 74, 78, 79, and 87 years), 37 repeats (aged 69 years), 38 repeats (aged 69 and 90 years), and 39 repeats (aged 67, 90, and 95 years). The detailed case histories of an exceptional case from this series will be presented: a 95-year-old man with 39 repeats who did not have classical features of HD. The apparently healthy survival into old age of some individuals with 36-39 repeats suggests that the HD mutation may not always be fully penetrant.This publication has 24 references indexed in Scilit:
- Increased instability of intermediate alleles in families with sporadic Huntington disease compared to similar sized intermediate alleles in the general populationHuman Molecular Genetics, 1995
- Mutational bias provides a model for the evolution of Huntington's disease and predicts a general increase in disease prevalenceNature Genetics, 1994
- A study of the Huntington's disease associated trinucleotide repeat in the Scottish population.Journal of Medical Genetics, 1993
- Evidence for a mechanism predisposing to intergenerational CAG repeat instability in spinocerebellar ataxia type INature Genetics, 1993
- Analysis of the huntingtin gene reveals a trinucleotide-length polymorphism in the region of the gene that contains two CCG-rich stretches and a correlation between decreased age of onset of Huntington's disease and CAG repeat numberHuman Molecular Genetics, 1993
- Relationship between trinucleotide repeat expansion and phenotypic variation in Huntington's diseaseNature Genetics, 1993
- A new polymerase chain reaction (PCR) assay for the trinucleotide repeat that is unstable and expanded on Huntington's disease chromosomesMolecular and Cellular Probes, 1993
- Novel Triplet Repeat Containing Genes in Human Brain: Cloning, Expression, and Length PolymorphismsGenomics, 1993
- Improved PCR conditions for the stretch of (CAG)n repeats causing Huntington's diseaseHuman Molecular Genetics, 1993
- Huntington's Disease: Two Families with Differing Clinical Features Show Linkage to the G8 ProbeScience, 1985