Intergenerational instability of the C9orf72 hexanucleotide repeat

The C9orf72 hexanucleotide repeat expansion (HRE) is the most common cause of amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD). It follows autosomal dominant inheritance in families; however, a high proportion of cases are sporadic, raising the possibility of parental premutation. We have demon strated that intermediatelength alleles (IAs) with ≥ 18 repeats (allele frequency ≈1%) belong to the same pool of haplotypes as the HRE, suggesting shared ancestry. Here, we tested whether alleles with ≥ 18 repeats expand in parental transmission. We used two repeatprimed PCR methods to analyze allele lengths in 539 genetically unselected parentoffspring pairs and in 152 pairs known to carry the SNP (rs139185008*C) that tags ≥ 18–20 repeat IAs and the HRE in Finland. We discovered intergenerational repeat length changes only in ≥ 20 repeat alleles. A significant (P = 0.0059) sex bias in 6–40 repeat alleles was noted using a logistic regression model. In this allele range, 12 out of 16 expansions were paternally inherited and 6 out of 7 contractions were maternally inherited. The expansion rate of 20–40 repeat alleles was 34 % in paternal and 11 % in maternal transmissions. In the 20–40 repeat range, most intergenerational expansions were 1–4 repeats in size (15/16), but one larger “jump”, a paternal expansion from 27 to 73 repeats, was observed. These results demonstrate that alleles with ≥ 20 repeats have an increased likelihood of instability, that a paternal expansion bias is observed in alleles with 20–40 repeats, and that expansion events are predominantly 1–4 repeats in size.