A CYS138-TO-ARG SUBSTITUTION IN THE GM2 ACTIVATOR PROTEIN IS ASSOCIATED WITH THE AB VARIANT FORM OF GM2 GANGLIOSIDOSIS

The AB-variant form of G(M2) gangliosidosis is an inherited lysosomal storage disease. Biochemical data have linked its cause to the lack of a functional G(M2) activator protein (activator). In the present study we identify a mutation in the gene encoding the activator protein of an AB-variant patient. These data represent direct evidence that the disease in the patient described here is a result of mutations at the Activator gene locus. A T412 --> C transition was found in the homozygous form in cDNA and genomic DNA from the patient. This nucleotide change would result in the substitution of Cys138 by an Arg residue in the activator protein. Whereas the patient's fibroblasts produce apparently normal levels of activator mRNA, they lack a functional activator protein. Transfection of either a construct containing the normal activator cDNA, pAct1, or a cDNA construct containing the T --> C transition caused COS-1 cells to transcribe high levels of activator mRNA. Lysates from cells transfected with pAct1 produced an elevated level of both pro- and mature forms of the activator protein, with an accompanying 11-fold enhancement in the ability of purified hexosaminidase A to hydrolyze G(M2) ganglioside. However, lysates from cells transfected with the mutant cDNA construct contained only low levels of the pro-activator protein, which failed to enhance hexosaminidase A activity significantly above the endogenous level of mock transfected COS cells. We conclude that the T412 --> C transition in the G(M2) Activator gene of the patient is responsible for the disease phenotype.