Key result
Long, highly polymorphic CAG and CTG repeats remain rare outside Triplet Repeat Expansion Diseases.
Why the study?
The allele distribution and factors responsible for intergenic and intragenic variability of trinucleotide repeats in human gene exons are not well understood.
Normal CAG/CTG repeat variation is now mapped across genes; leaves open any role in disease risk or phenotypic diversity.
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.
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Rozanska et al. (2007) studied this question. CAG and CTG repeats was evaluated. Analysis of CAG and CTG repeats in human genes revealed that very long and highly polymorphic repeats are infrequent outside of Triplet Repeat Expansion Diseases.
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