Identifying a novel genetic modifier for cataracts in mouse genetic models
Cataracts are the leading cause of blindness worldwide. 53% of all Americans over the age of 75 have cataracts or have had cataract extraction surgery. Connexin protein subunits form gap junction channels in the lens and transport metabolites required for lens transparency. Previous work has indicated that when connexin is knocked out in the 129SvJae mouse strain, severe cataracts results. Disruption of the same connexin in the C57BL/6J (B6) strain displays a mild cataract that is hardly noticeable. Several loci in the B6 background likely containing genes that function to suppress cataract severity have been mapped; one of these genes is a cytoskeletal scaffolding protein called periaxin. We have hypothesized that a gene recently mapped to mouse chromosome 2 is a membrane/cytoskeleton complex related to periaxin. I hope to test this hypothesis and, in the process, identify a new gene that acts as a second genetic modifier for cataract formation.
Message to Sponsor
- Major: Molecular and Cell Biology: Cell and Developmental Biology
- Sponsor: Pergo SURF fellow
- Mentor: Xiaohua Gong, Optometry