Distribution and characterization of a Sandhoff disease-associated 50-kb deletion in the gene encoding the human beta-hexosaminidase beta-chain

Hum Genet. 1990 Aug;85(3):327-9. doi: 10.1007/BF00206756.

Abstract

A 50-kb deletion was demonstrated in the gene encoding for the beta-subunit of human hexosaminidase (HEXB), using field inversion gel electrophoresis (FIGE) of SfiI-digested chromosomal DNA from patients with Sandhoff disease. We investigated 14 patients from different parts of Europe and found no deletion in 5 patients, 2 patients homozygous for the deletion, and 7 patients with the deletion in one allele. The distribution of the 50-kb deletion was approximately in agreement with the Hardy-Weinberg equilibrium. The deletion was characterized using chromosomal DNA from one of the two homozygous patients. Restriction fragments were hybridized with a 1.6-kb (almost complete) and a 0.4-kb (5') HEXB cDNA clone. It appeared that the deletion started in intron 5, extending in the 5' direction and causing the loss of exon 1-5 and the promoter area of the HEXB gene.

MeSH terms

  • Chromosome Deletion*
  • Europe
  • Genetic Testing
  • Hexosaminidase B
  • Homozygote
  • Humans
  • Polymorphism, Restriction Fragment Length
  • Restriction Mapping
  • Sandhoff Disease / genetics*
  • beta-N-Acetylhexosaminidases / genetics*

Substances

  • Hexosaminidase B
  • beta-N-Acetylhexosaminidases