Mutations in the PAX6 gene in patients with hereditary aniridia

Alison Davis, John K.cowell

Research output: Contribution to journalArticle

60 Citations (Scopus)

Abstract

The 14 exons of the PAX6 gene have been analysed exon-by-exon using SSCP in 6 aniridla families. In each family band shifts were observed on the SSCP gels for only one exon and direct PCR-sequencing revealed mutations in each case. Two mutations involved C-T transitions in CGAarg codons in exons 9 and 11. Another C-T transition converted a CAG-glutamine to a TAG-stop in exon 7. Small insertions created frameshifts which produced downsteam stop codons in another two patients and an A-T mutation disrupted the splice donor site of exon 5 in the remaining family. Thus, complete inactivation of the PAX6 gene is predicted in all cases. Analysis of other affected members of the families showed that, in each case, all affected individuals carried the same family-specific mutation. One polymorphism was found in exon 7. This data strongly supports the candidature of PAX6 as the gene responsible for hereditary aniridia.

Original languageEnglish (US)
Pages (from-to)2093-2097
Number of pages5
JournalHuman Molecular Genetics
Volume2
Issue number12
DOIs
StatePublished - Dec 1 1993
Externally publishedYes

Fingerprint

Aniridia
Exons
Mutation
Genes
Single-Stranded Conformational Polymorphism
RNA Splice Sites
Terminator Codon
Gene Silencing
Glutamine
Codon
Gels
Polymerase Chain Reaction

ASJC Scopus subject areas

  • Molecular Biology
  • Genetics
  • Genetics(clinical)

Cite this

Mutations in the PAX6 gene in patients with hereditary aniridia. / Davis, Alison; K.cowell, John.

In: Human Molecular Genetics, Vol. 2, No. 12, 01.12.1993, p. 2093-2097.

Research output: Contribution to journalArticle

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