The GAA triplet-repeat sequence in Friedreich ataxia shows a high a level of somatic instability in vivo, with a significant predilection for large contractions

Rajesh Sharma, Saeeda Bhatti, Mariluz Gomez, Rhonda M. Clark, Cynthia Murray, Tetsuo Ashizawa, Sanjay I. Bidichandani

Research output: Contribution to journalArticlepeer-review

53 Scopus citations

Abstract

Friedreich ataxia is commonly caused by large expansions of a GAA triplet-repeat (GAA-TR) sequence in the first intron of the FRDA gene. We used small-pool PCR to analyze somatic variability among 7190 individual FRDA molecules from peripheral blood DNA of subjects carrying 12 different expanded alleles, ranging in size from 241 to 1105 triplets. Expanded alleles showed a length-dependent increase in somatic variability, with mutation loads ranging from 47% to 78%. We noted a strong contraction bias among long alleles (>500 triplets), which showed a 4-fold higher frequency of large contractions versus expansions. Some contractions were very large; of all somatic mutations scored, ∼5% involved contractions of >50% of the original allele length, and 0.29% involved complete reversion to the normal/premutation length (≤60 triplets). These observations contrast sharply with the strong expansion bias seen in expanded CTG triplet repeats in myotonic dystrophy. No somatic variability was detected in >6000 individual FRDA molecules analyzed from 15 normal alleles (8-25 triplets). A premutation allele with 44 uninterrupted GAA repeats was found to be unstable, ranging in size from 6 to 113 triplets, thus establishing the threshold for somatic instability between 26 and 44 GAA triplets. Analysis of an additional 7850 FRDA molecules from serially passaged lymphoblastoid cell lines carrying nine expanded alleles (132-933 triplets) showed very low mutation loads, ranging from 0% to 6.2%. Our data indicate that expanded GAA-TR alleles in Friedreich ataxia are highly mutable and have a natural tendency to contract in vivo, and that these properties depend on multiple factors, including DNA sequence, triplet-repeat length and unknown cell-type-specific factors.

Original languageEnglish (US)
Pages (from-to)2175-2187
Number of pages13
JournalHuman Molecular Genetics
Volume11
Issue number18
StatePublished - Sep 1 2002

ASJC Scopus subject areas

  • Molecular Biology
  • Genetics
  • Genetics(clinical)

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