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Keeping an eye on glaucoma

Jonathan B Weitzman

Author Affiliations

Genome Biology 2003, 4:spotlight-20030307-02  doi:10.1186/gb-spotlight-20030307-02


The electronic version of this article is the complete one and can be found online at:


Published:7 March 2003

© 2003 BioMed Central Ltd

Research news

Glaucoma is the leading cause of irreversible blindness and affects millions worldwide. Patients with primary congenital glaucoma (PCG) often have mutations in the cytochrome P450 family 1, subfamily B, polypeptide 1 (CYP1B1) gene. In the March 7 Science, Libby et al. report the characterization of a Cyp1b1-/- knockout mouse as a model for PCG (Science 2003, 299:1578-1581). The mice had developmental eye defects similar to those seen in human patients. Genetic and histological analysis revealed a role for the tyrosinase gene as a genetic modifier. Tyrosinase also modifies the anterior segment dysgenesis phenotypes observed in mice lacking the Foxc1 gene that has also been implicated in PCG. Tyrosinase converts tyrosine to L-dopa, and the ocular phenotypes of the knockout mice could be relieved by the administration of L-dopa. This study suggests that L-dopa should be tested as a possible therapeutic for treating glaucoma patients.

References

  1. Anterior segment dysgenesis and the developmental glaucomas are complex traits.

    PubMed Abstract | Publisher Full Text OpenURL

  2. Phenotype of cytochrome P4501B1 gene (CYP1B1) mutations in Japanese patients with primary congenital glaucoma.

    PubMed Abstract | Publisher Full Text OpenURL

  3. [http://www.sciencemag.org] webcite

    Science