Investigation of founder effects for the Thr377Met Myocilin mutation in glaucoma families from differing ethnic backgrounds

The aim of this study was to determine if there is a common founder for the Thr377Met myocilin mutation in primary open angle glaucoma (POAG) families with various ethnic backgrounds. Genomic DNA of 24 POAG-affected individuals from nine pedigrees with the Thr377Met mutation and 104 unaffected famil...

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Bibliographic Details
Published in:Molecular vision 2007-03, Vol.13, p.487-492
Main Authors: Hewitt, Alex W, Samples, John R, Allingham, R Rand, Järvelä, Irma, Kitsos, George, Krishnadas, Subbaiah R, Richards, Julia E, Lichter, Paul R, Petersen, Michael B, Sundaresan, Periasamy, Wiggs, Janey L, Mackey, David A, Wirtz, Mary K
Format: Article
Language:English
Subjects:
Adult
Australia - ethnology
Cytoskeletal Proteins - genetics
Europe - ethnology
Eye Proteins - genetics
Founder Effect
Glaucoma, Open-Angle - ethnology
Glaucoma, Open-Angle - genetics
Glycoproteins - genetics
Haplotypes
Humans
Linkage Disequilibrium
Methionine
Microsatellite Repeats
Middle Aged
Mutation
Polymorphism, Single Nucleotide
Threonine
United States - ethnology
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Summary:The aim of this study was to determine if there is a common founder for the Thr377Met myocilin mutation in primary open angle glaucoma (POAG) families with various ethnic backgrounds. Genomic DNA of 24 POAG-affected individuals from nine pedigrees with the Thr377Met mutation and 104 unaffected family members was genotyped with six microsatellite markers and four single nucleotide polymorphisms. The families were from Greece, India, Finland, the USA, and Australia. To assess the degree of linkage disequilibrium across MYOC in the general population we also investigated data generated from the HapMap consortium. Three distinct haplotypes associated with the Thr377Met myocilin mutation were identified. The families from the USA and Greece, as well as the three Australian families originating from Greece and the former Yugoslavian Republic of Macedonia had one common haplotype. Interestingly, however, HapMap data suggest that linkage disequilibrium across MYOC was not strong. The Thr377Met myocilin mutation has arisen at least three separate times. Evidence for genetic founder effects in this prevalent age-related, yet heterogeneous, disease has important implications for future gene identification strategies.
ISSN:1090-0535