Characterization of EcoRI mutation in fucosidosis patients: A stop codon in the open reading frame
- Cite this article as:
- Kretz, K.A., Darby, J.K., Willems, P.J. et al. J Mol Neurosci (1989) 1: 177. doi:10.1007/BF02918904
Recently, a subset of fucosicosis patients was identified in which the single EcoRI site in the open reading frame of the human cDNA encoding α-l-fucosidase was obliterated. We have employed the polymerase chain reaction technique to amplify α-l-fucosidase DNA from the five patients known to carry the EcoRI abnormality as well as four patients and two additional fucosidosis patients who do not carry the EcoRI abnormality. Sequence analysis of the amplified DNA has determined that the EcoRI site was destroyed by a C-T transition in the last position of the EcoRI site. This single base change results in the generation of a stop codon 120 base pairs upstream of the normal stop codon. In addition, we have determined that EcoRI cleavage of amplified DNA may be a useful diagnostic tool in the diagnosis of heterozygotes and in prenatal diagnosis of fetuses at risk for this disease.