Identification of a novel splice-site mutation in MIP in a Chinese congenital cataract family

PURPOSE: To map the locus and identify the gene causing autosomal dominant congenital cataract (ADCC) with “snail-like” phenotype in a large Chinese family. METHODS: Clinical and ophthalmologic examinations were conducted on family members and documented by slit lamp photography. Linkage analysis was performed with an initial 41 microsatellite markers, then 3 additional markers flanking the major intrinsic protein (MIP) gene. Mutations were screened by DNA sequencing and verified by restriction fragment length polymorphism (RFLP) analysis. RESULTS: Significant two-point LOD scores were obtained at 5 markers flanking MIP with the highest 3.08 (θ=0.00) at marker D12S1632. Mutation screening of MIP identified a heterozygous G>A transition at the acceptor splice site of intron 3 (IVS3 −1 G>A), abolishing a BstSF I restriction site in one allele of all the affected individuals. CONCLUSIONS: We identified a novel splice-site mutation (IVS3 −1 G>A in MIP) in a Chinese ADCC family. To our knowledge, this is the first report on an acceptor splice-site mutation in human genes associated with ADCC.