K. Honke et al., AN ADULT-TYPE METACHROMATIC LEUKODYSTROPHY CAUSED BY SUBSTITUTION OF SERINE FOR GLYCINE-122 IN ARYLSULFATASE-A, Human genetics, 92(5), 1993, pp. 451-456
Metachromatic leukodystrophy (MLD) is a lysosomal storage disease with
autosomal recessive inheritance caused by a deficiency of the enzyme
arylsulfatase A (ASA). We have identified a new mutation in the ASA ge
ne of a patient with adult-type MLD. In this mutation, the glycine at
position 122, a highly conserved residue in the AS gene family, was re
placed by serine. In a transient expression study, COS cells transfect
ed with the mutant cDNA carrying 122Gly-->Ser did not show an increase
of ASA activity and produced little material immunoreactive to an ant
i-ASA antibody, despite normal mRNA levels.