Journal of Molecular Neuroscience

, Volume 1, Issue 3, pp 177–180

Characterization of EcoRI mutation in fucosidosis patients: A stop codon in the open reading frame

  • Keith A. Kretz
  • John K. Darby
  • Patrick J. Willems
  • John S. O'Brien
Article

DOI: 10.1007/BF02918904

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

Abstract

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.

Copyright information

© Humana Press Inc. 1989

Authors and Affiliations

  • Keith A. Kretz
    • 1
  • John K. Darby
    • 2
  • Patrick J. Willems
    • 1
  • John S. O'Brien
    • 1
  1. 1.Department of Neurosciences and Center for Molecular GeneticsUniversity of California, San DiegoLa JollaUSA
  2. 2.Department of Genetics and NeurobiologyStanford University School of MedicineStanfordUSA
  3. 3.Department of Medical GeneticsUniversity of AntwerpWilrijkBelgium