A novel PAX6 gene mutation in an Indian aniridia patient

Mol Vis. 2003 May 29:9:205-9.

Abstract

Purpose: A mutation in the PAX6 gene is thought to be the genetic cause of aniridia. Here we search for PAX6 gene mutations in Indian aniridia patients.

Methods: We amplified the coding exons of the PAX6 gene from the genomic DNA of 15 unrelated aniridia patients using polymerase chain reaction technology. We then performed single-strand conformation polymorphism analysis and heteroduplex analysis to search for sequence variants.

Results: Sequencing of shifted bands in two patients revealed PAX6 gene mutations. One of these was a novel mutation, 1180insA, located in exon 10 at the start of the PST domain. The other mutation, 1080C->T (R240X), located in exon 9 within the homeodomain, and is another example of the most commonly reported PAX6 mutation.

Conclusions: Although PAX6 gene mutations and polymorphisms have been reported from various ethnic groups, we report for the first time the identification of PAX6 gene mutations in Indian aniridia patients.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Amino Acid Sequence
  • Aniridia / ethnology
  • Aniridia / genetics*
  • Cataract / genetics
  • DNA Mutational Analysis
  • Eye Proteins / genetics*
  • Glaucoma / genetics
  • Heteroduplex Analysis
  • Homeodomain Proteins / genetics*
  • Humans
  • India / epidemiology
  • Male
  • Molecular Sequence Data
  • Mutation*
  • Nystagmus, Pathologic / genetics
  • PAX6 Transcription Factor
  • Paired Box Transcription Factors
  • Polymerase Chain Reaction
  • Polymorphism, Single-Stranded Conformational
  • Repressor Proteins
  • Sequence Analysis, Protein
  • Transcription Factors / genetics*

Substances

  • Eye Proteins
  • Homeodomain Proteins
  • PAX6 Transcription Factor
  • PAX6 protein, human
  • Paired Box Transcription Factors
  • Repressor Proteins
  • Transcription Factors