Mutation Screen of the Membrane-Type Frizzled-Related Protein (MFRP) Gene in Patients with Inherited Retinal Degenerations

• Published in: Ophthalmic genetics 2005-12, Vol.26 (4), p.157-161
• Main Authors: Pauer, Gayle J. T., Xi, Quansheng, Zhang, Kang, Traboulsi, Elias I., Hagstrom, Stephanie A.
• Format: Article
• Language: English
• Subjects: 5' Untranslated Regions - genetics; Case-Control Studies; DNA Mutational Analysis; Female; frizzled; Humans; Introns - genetics; Male; Membrane Proteins - genetics; MFRP; mutation; Mutation, Missense - genetics; Optic Atrophy, Hereditary, Leber - genetics; Pedigree; Polymerase Chain Reaction; Polymorphism, Genetic; Polymorphism, Single-Stranded Conformational; Retinal degeneration; Retinal Degeneration - genetics
• ISSN: 1381-6810; 1744-5094
• DOI: 10.1080/13816810500374425

MFRP is a member of the frizzled-related protein family and contains a cysteine-rich domain essential for Wnt binding and signaling. MFRP is highly expressed in the retinal pigment epithelial cells of the eye. A splice donor mutation in the mouse ortholog of Mfrp is responsible for photoreceptor degeneration in the rd6 mouse. For these reasons, we investigated MFRP as a candidate gene for a phenotype associated with mutations. We screened 152 patients with inherited retinal degenerations including retinitis pigmentosa, Leber congenital amaurosis and Stargardt macular dystrophy. We identified five polymorphisms in the 5′ untranslated region, four missense changes, six isocoding variants and four intronic changes. None of the sequence variants were interpreted as pathogenic.