Journal Article

Microarray-based mutation analysis of the ABCA4 (ABCR) gene in autosomal recessive cone–rod dystrophy and retinitis pigmentosa

Born, L Ingeborgh van den, Hoyng, Carel B, Yzer, Suzanne, Cremers, Frans PM, Allikmets, Rando, Klevering, B Jeroen, Rohrschneider, Klaus, Zonneveld, Marijke, Maugeri, Alessandra

2004

Overview

Mutations in the ABCA4 gene have been associated with autosomal recessive Stargardt disease (STGD1), cone–rod dystrophy (CRD), and retinitis pigmentosa (RP). We employed a recently developed genotyping microarray, the ABCR400-chip, to search for known ABCA4 mutations in patients with isolated or autosomal recessive CRD (54 cases) or RP (90 cases). We performed detailed ophthalmologic examinations and identified at least one ABCA4 mutation in 18 patients (33%) with CRD and in five patients (5.6%) with RP. Single-strand conformation polymorphism (SSCP) analysis and subsequent DNA sequencing revealed four novel missense mutations (R24C, E161K, P597S, G618E) and a novel 1-bp deletion (5888delG). Ophthalmoscopic abnormalities in CRD patients ranged from minor granular pigmentary changes in the posterior pole to widespread atrophy. In 12 patients with recordable electroretinogram (ERG) tracings, a cone–rod pattern was detected. Three patients demonstrated progression from a retinal dystrophy resembling STGD1 to a more widespread degeneration, and were subsequently diagnosed as CRD. In addition to a variable degree of atrophy, all RP patients displayed ophthalmologic characteristics of classic RP. When detectable, ERG recordings in these patients demonstrated rod–cone patterns of photoreceptor degeneration. In conclusion, in this study, we show that the ABCA4 mutation chip is an efficient first screening tool for arCRD.

• Publisher: Springer International Publishing,Nature Publishing,Nature Publishing Group
• Subject: ATP-Binding Cassette Transporters - genetics / Atrophy / Bioinformatics / Biological and medical sciences / Biomedical and Life Sciences / Biomedicine / Clonal deletion / Conformation / Cytogenetics / Disease / DNA microarrays / DNA Mutational Analysis / DNA sequencing / Dystrophy / Electroretinograms / Gene deletion / Gene Expression / Genetics / Genotyping / Human Genetics / Humans / Macular degeneration / Medical sciences / Missense mutation / Mutation / Oligonucleotide Array Sequence Analysis / Ophthalmology / Patients / Phenotype / Proteins / Retina / Retina - pathology / Retinal degeneration / Retinitis / Retinitis pigmentosa / Retinitis Pigmentosa - genetics / Retinitis Pigmentosa - physiopathology / Retinopathies / Studies