A novel intronic mutation of the TAZ ( G4.5) gene in a patient with Barth syndrome: creation of a 5' splice donor site with variant GC consensus and elongation of the upstream exon

Hum Genet. 2001 Nov;109(5):559-63. doi: 10.1007/s00439-001-0612-3. Epub 2001 Oct 13.

Abstract

Mutation analysis of the TAZ ( G4.5) gene was performed on a patient with Barth syndrome. The reverse transcription/polymerase chain reaction procedure showed aberrant splicing and elongation of exon 3 because of the insertion of 106 bases (IVS3+1 to +106) between exons 3 and 4. The genomic DNA revealed an intronic mutation four bases downstream from the new cleavage site (IVS3+110G-->A). The IVS3+110G-->A mutation created a novel 5' splice site that showed GC but not GT, and the additional splice site was used preferentially over the upstream authentic slice site. This is a new type of splicing mutation responsible for a human genetic disease.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Abnormalities, Multiple / genetics*
  • Acyltransferases
  • Animals
  • Base Sequence
  • COS Cells
  • DNA Primers
  • DNA-Binding Proteins / genetics*
  • Exons*
  • Humans
  • Introns*
  • Mutation*
  • Polymerase Chain Reaction
  • Proteins*
  • Syndrome
  • Transcription Factors / genetics*

Substances

  • DNA Primers
  • DNA-Binding Proteins
  • Proteins
  • Transcription Factors
  • Acyltransferases
  • TAFAZZIN protein, human