Two novel missense mutations in the cystathionine beta-synthase gene in homocystinuric patients

Hum Genet. 1995 Aug;96(2):249-50. doi: 10.1007/BF00207394.

Abstract

Direct sequencing of the coding region of the cystathionine beta-synthase (CBS) gene in two homocystinuric patients revealed the presence of two novel missense mutations. The first mutation, a 1111G-->A transition, resulted in the substitution of the evolutionary conserved valine-371 by a methionine residue (V371M) and created a new NlaIII restriction site. The second mutation, a G-->A transition at base-pair 494, resulted in an amino acid change from cysteine to tyrosine (C165Y) and abolished a BsoFI restriction site. Both mutations were found in a compound heterozygous state with the previously described 833T-->C transition.

Publication types

  • Case Reports
  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Amino Acid Sequence
  • Base Sequence
  • Cystathionine beta-Synthase / genetics*
  • Heterozygote
  • Homocystinuria / enzymology
  • Homocystinuria / genetics*
  • Humans
  • Male
  • Molecular Sequence Data
  • Point Mutation*
  • Polymerase Chain Reaction
  • Reading Frames / genetics
  • Sequence Homology, Amino Acid
  • Species Specificity

Substances

  • Cystathionine beta-Synthase