Exon skipping caused by a base substitution at a splice site in the GTP cyclohydrolase I gene in a Japanese family with hereditary progressive dystonia dopa responsive dystonia

Biochem Biophys Res Commun. 1995 Aug 15;213(2):645-51. doi: 10.1006/bbrc.1995.2180.

Abstract

We report a novel mutation at a splice site in the GTP cyclohydrolase I gene in a Japanese family with hereditary progressive dystonia with marked diurnal fluctuation (HPD)/dopa responsive dystonia (DRD). Reverse transcriptase-initiated PCR (RT-PCR) of lymphocyte mRNA showed both normal and small size fragments in the HPD patient and his asymptomatic mother. Sequence analysis revealed that skip splicing of exon 1 to exon 3 occurred in the small fragment. The patient and his mother were heterozygous for G --> C substitution at conserved consensus sequence GT at 5' end of the intron 2. Quantitative RT-PCR showed that the expression of normal GTP cyclohydrolase I mRNA decreased in their lymphocytes, while the HPD patient had more expression of mutant GTP cyclohydrolase I mRNA than his asymptomatic mother.

Publication types

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

MeSH terms

  • Adult
  • Base Sequence
  • Dystonia / drug therapy
  • Dystonia / genetics*
  • Exons*
  • Frameshift Mutation
  • GTP Cyclohydrolase / genetics*
  • Humans
  • Japan
  • Levodopa / therapeutic use*
  • Male
  • Molecular Sequence Data
  • Mutation*
  • Polymerase Chain Reaction
  • RNA Splicing*
  • RNA, Messenger / chemistry
  • RNA, Messenger / genetics
  • RNA-Directed DNA Polymerase

Substances

  • RNA, Messenger
  • Levodopa
  • RNA-Directed DNA Polymerase
  • GTP Cyclohydrolase