Identification of a nonsense mutation in the PAX9 gene in molar oligodontia

Eur J Hum Genet. 2001 Oct;9(10):743-6. doi: 10.1038/sj.ejhg.5200715.

Abstract

Development of dentition is controlled by numerous genes, as has been shown by experimental animal studies and mutations that have been identified by genetic studies in man. Here we report a nonsense mutation in the PAX9 gene that is associated with molar tooth agenesis in a Finnish family. The A340T transversion creates a stop codon at lysine 114, and truncates the coded PAX9 protein at the end of the DNA-binding paired-box. All the affected members of the family were heterozygous for the mutation. The tooth agenesis phenotype involves all permanent second and third molars and most of the first molars and resembles the earlier reported phenotype that was also associated with a PAX9 mutation. The phenotype is presumably a consequence of haploinsufficiency of PAX9. In another Finnish family with molar tooth agenesis, we could not find similar sequence changes in PAX9.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Anodontia / genetics*
  • Base Sequence
  • Child
  • Codon, Nonsense / genetics*
  • DNA Mutational Analysis
  • DNA-Binding Proteins / genetics*
  • Female
  • Finland
  • Humans
  • Male
  • Molar / abnormalities*
  • PAX9 Transcription Factor
  • Pedigree
  • Phenotype
  • Transcription Factors / genetics*

Substances

  • Codon, Nonsense
  • DNA-Binding Proteins
  • PAX9 Transcription Factor
  • PAX9 protein, human
  • Transcription Factors