MOLECULAR HETEROGENEITY IN MUCOPOLYSACCHARIDOSIS IVA IN AUSTRALIA ANDNORTHERN-IRELAND - 9 NOVEL MUTATIONS INCLUDING T312S, A COMMON ALLELETHAT CONFERS A MILD PHENOTYPE
N. Yamada et al., MOLECULAR HETEROGENEITY IN MUCOPOLYSACCHARIDOSIS IVA IN AUSTRALIA ANDNORTHERN-IRELAND - 9 NOVEL MUTATIONS INCLUDING T312S, A COMMON ALLELETHAT CONFERS A MILD PHENOTYPE, Human mutation, 11(3), 1998, pp. 202-208
Mucopolysaccharidosis IVA (MPS IVA) is an autosomal recessive lysosoma
l storage disorder caused by a genetic defect in N-acetylgalactosamine
-6-sulfate sulfatase (GALNS). Previous studies of patients from a Brit
ish-Irish population showed that the I113F mutation is the most common
single mutation among MPS IVA patients and produces a severe clinical
phenotype. We studied mutations in the GALNS gene from 23 additional
MPS IVA patients (15 from Australia, 8 from Northern Ireland), with va
rious clinical phenotypes (severe, 16 cases; intermediate, 4 cases; mi
ld, 3 cases). We found two common mutations that together accounted fo
r 32% of the 44 unrelated alleles in these patients. One is the T312S
mutation, a novel mutation found exclusively in milder patients. The o
ther is the previously described I113F that produces a severe phenotyp
e. The I113F and T312S mutations accounted for 8 (18%) and 6 (14%) of
44 unrelated alleles, respectively. The relatively high residual GALNS
activity seen when the T312S mutant cDNA is overexpressed in mutant c
ells provides an explanation for the mild phenotype in patients with t
his mutation. The distribution and relative frequencies of the I113F a
nd T312S mutations in Australia corresponded to those observed in Nort
hern Ireland and are unique to these two populations, suggesting that
both mutations were probably introduced to Australia by Irish migrants
during the 19th century. Haplotype analysis using 6 RFLPs provides ad
ditional data that the I113F mutation originated from a common ancesto
r. The other 9 novel mutations identified in these 23 patients were ea
ch limited to a single family. These data provide further evidence for
extensive allelic heterogeneity in MPS IVA in British-Irish patients
and provide evidence for their transmission to Australia by British-Ir
ish migrants. (C) 1998 Wiley Liss, Inc.