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Unstable familial transmissions of Huntington disease alleles with 27–35 CAG repeats (intermediate alleles)

A. Semaka, J.A. Collins, M.R. Hayden · American Journal of Medical Genetics Part B: Neuropsychiatric Genetics · 2009

AbstractThere are inconsistent reports regarding the likelihood of repeat instability for alleles with 27–35 CAG repeats in the Huntington disease (HD) gene. We have examined the intergenerational stability of such intermediate alleles in 51 families from the University of British Columbia's DNA and Tissue Bank for Huntington Disease Research (UBC‐HD Databank). A total of 181 transmissions were identified, with 30% (n = 54/181) of the alleles being unstable upon transmission. The unstable transmissions included both expansions (n = 37) and contractions (n = 17) of CAG size. Of the expanded alleles, 68% (n = 25/37) expanded into the HD range (>36 CAG). Therefore, 14% (n = 25/181) of the 27–35 CAG allele transmissions examined expanded into the disease‐associated range resulting in a new mutation for HD. Significantly, of these new mutations, 40% (n = 10/25) originated from an allele with 35 CAG repeats with CAG repeat expansions ranging from +1 CAG to +23 CAG. The proportion of new mutations in the UBC‐HD Databank is consistent with the most recent new mutation rate for HD, estimated to be at least 10%. The observed difference in the stability of HD intermediate allele transmissi

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