EPHA2 is associated with age-related cortical cataract in mice and humans

Gyungah Jun, Hong Guo, Barbara E.K. Klein, Ronald Klein, Jin Wang Jie, Paul Mitchell, Hui Miao, Kristine E. Lee, Tripti Joshi, Matthias Buck, Preeti Chugha, David Bardenstein, Alison P. Klein, Joan E. Bailey-Wilson, Xiaohua Gong, Tim D. Spector, Toby Andrew, Christopher J. Hammond, Robert C. Elston, Sudha K. IyengarBingcheng Wang

Research output: Contribution to journalArticle

Abstract

Age-related cataract is a major cause of blindness worldwide, and cortical cataract is the second most prevalent type of agerelated cataract. Although a significant fraction of age-related cataract is heritable, the genetic basis remains to be elucidated. We report that homozygous deletion of Epha2 in two independent strains of mice developed progressive cortical cataract. Retroillumination revealed development of cortical vacuoles at one month of age; visible cataract appeared around three months, which progressed to mature cataract by six months. EPHA2 protein expression in the lens is spatially and temporally regulated. It is low in anterior epithelial cells, upregulated as the cells enter differentiation at the equator, strongly expressed in the cortical fiber cells, but absent in the nuclei. Deletion of Epha2 caused a significant increase in the expression of HSP25 (murine homologue of human HSP27) before the onset of cataract. The overexpressed HSP25 was in an underphosphorylated form, indicating excessive cellular stress and protein misfolding. The orthologous human EPHA2 gene on chromosome 1p36 was tested in three independent worldwide Caucasian populations for allelic association with cortical cataract. Common variants in EPHA2 were found that showed significant association with cortical cataract, and rs6678616 was the most significant in meta-analyses. In addition, we sequenced exons of EPHA2 in linked families and identified a new missense mutation, Arg721Gln, in the protein kinase domain that significantly alters EPHA2 functions in cellular and biochemical assays. Thus, converging evidence from humans and mice suggests that EPHA2 is important in maintaining lens clarity with age.

Original languageEnglish (US)
Article numbere1000584
JournalPLoS genetics
Volume5
Issue number7
DOIs
StatePublished - Jul 2009

ASJC Scopus subject areas

  • Ecology, Evolution, Behavior and Systematics
  • Molecular Biology
  • Genetics
  • Genetics(clinical)
  • Cancer Research

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    Jun, G., Guo, H., Klein, B. E. K., Klein, R., Jie, J. W., Mitchell, P., Miao, H., Lee, K. E., Joshi, T., Buck, M., Chugha, P., Bardenstein, D., Klein, A. P., Bailey-Wilson, J. E., Gong, X., Spector, T. D., Andrew, T., Hammond, C. J., Elston, R. C., ... Wang, B. (2009). EPHA2 is associated with age-related cortical cataract in mice and humans. PLoS genetics, 5(7), [e1000584]. https://doi.org/10.1371/journal.pgen.1000584