Novel single-base deletional mutation in major intrinsic protein (MIP) in autosomal dominant cataract

Am J Ophthalmol. 2006 Apr;141(4):761-3. doi: 10.1016/j.ajo.2005.11.008.


Purpose: To further elucidate the cataract phenotype, and identify the gene and mutation for autosomal dominant cataract (ADC) in an American family of European descent (ADC2) by sequencing the major intrinsic protein gene (MIP), a candidate based on linkage to chromosome 12q13.

Design: Observational case series and laboratory experimental study.

Methods: We examined two at-risk individuals in ADC2. We PCR-amplified and sequenced all four exons and all intron-exon boundaries of the MIP gene from genomic and cloned DNA in affected members to confirm one variant as the putative mutation.

Results: We found a novel single deletion of nucleotide (nt) 3223 (within codon 235) in exon four, causing a frameshift that alters 41 of 45 subsequent amino acids and creates a premature stop codon.

Conclusions: We identified a novel single base pair deletion in the MIP gene and conclude that it is a pathogenic sequence alteration.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Aquaporins / genetics*
  • Base Sequence*
  • Cataract / genetics*
  • Chromosomes, Human, Pair 12 / genetics
  • Codon / genetics
  • DNA Mutational Analysis
  • Eye Proteins / genetics*
  • Female
  • Frameshift Mutation / genetics*
  • Genes, Dominant
  • Genetic Linkage
  • Humans
  • Male
  • Membrane Glycoproteins / genetics*
  • Pedigree
  • Phenotype
  • Polymerase Chain Reaction
  • Sequence Deletion / genetics*


  • Aquaporins
  • Codon
  • Eye Proteins
  • Membrane Glycoproteins
  • aquaporin 0