CAG and CTG repeat polymorphism in exons of human genes shows distinct features at the expandable loci

Matylda Rozanska, Krzysztof Sobczak, Anna Jasinska, Marek Napierala, Danuta Kaczynska, Anna Czerny, Magdalena Koziel, Piotr Kozlowski, Marta Olejniczak, Wlodzimierz J. Krzyzosiak

Research output: Contribution to journalArticlepeer-review

15 Scopus citations

Abstract

Although the trinucleotide repeats are present in the exons of numerous human genes, the allele distribution is not well known, and the factors responsible for their intergenic and intragenic variability are not well understood. We have analyzed the length and sequence variation within the most commonly occurring CAG and CTG repeats in a large number of human genes selected to contain the longest reported repeat tracts. Our study revealed that in genes other than those implicated in the Triplet Repeat Expansion Diseases (TREDs), the very long and highly polymorphic repeats are rather infrequent. The length of pure repeat tract in the most frequent allele was found to correlate well with the rate of the repeat length polymorphism, and CAA triplets were shown to be the most frequent CAG repeat interruptions. As both the CAG and CAA triplets code for glutamine, our results may suggest that the selective pressure disfavors the long uninterrupted CAG repeats in genes and transcripts but not the long normal polyglutamine tracts in proteins. This may indicate that hairpin structures formed in ssDNA and RNA by long pure CAG repeats would be selected against as they may impede normal cellular processes.

Original languageEnglish (US)
Pages (from-to)451-458
Number of pages8
JournalHuman mutation
Volume28
Issue number5
DOIs
StatePublished - May 2007
Externally publishedYes

Keywords

  • Human genetic variation
  • Microsatellite genotyping
  • Repeat instability

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

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