A common point mutation in the tyrosine hydroxylase gene in autosomal recessive L-DOPA-responsive dystonia in the Dutch population

Hum Genet. 1998 Jun;102(6):644-6. doi: 10.1007/s004390050756.

Abstract

This report concerns one new mutation in the tyrosine hydroxylase (TH) gene in three patients originating from three unrelated Dutch families with autosomal recessive L-DOPA-responsive dystonia (DRD). In this study, all exons of the TH gene were amplified by the polymerase chain reaction and subjected to analyses by single-strand conformation polymorphism. An aberrant migration pattern was observed for exon 6 of the TH gene in all patients. Direct sequencing of the coding region of exon 6 revealed the presence of one novel missense mutation. An a698g transition resulted in the substitution of the evolutionary conserved arginine 233 by a histidine (R233H). All patients were homozygous for the mutation. This new mutation in the TH gene was confirmed by restriction enzyme analysis with the restriction enzyme HhaI. Thus, a high proportion of defective TH alleles may be R233H in The Netherlands.

MeSH terms

  • Chromosomes, Human, Pair 11
  • Denmark
  • Dystonia / drug therapy
  • Dystonia / enzymology
  • Dystonia / genetics*
  • Genes, Recessive
  • Humans
  • Levodopa / therapeutic use
  • Point Mutation*
  • Polymorphism, Single-Stranded Conformational
  • Tyrosine 3-Monooxygenase / genetics*

Substances

  • Levodopa
  • Tyrosine 3-Monooxygenase