Variant in EZR leads to defects in lens development.

BACKGROUND

Congenital cataract is a common cause of blindness. Genetic factors always play important role.

MATERIAL AND

METHODS

This study identified a novel missense variant (c.1412C>T (p.P471L)) in the EZR gene in a four-generation Chinese family with nuclear cataract by linkage analysis and whole-exome sequencing. A knockout study in zebrafish using transcription activator-like effector nucleases was carried out to gain insight into candidate gene function.

RESULTS

Conservative and functional prediction suggests that the P-to-L substitution may impair the function of the human ezrin protein. Histology showed developmental delays in the ezrin-mutated zebrafish, manifesting as multilayered lens epithelial cells. Immunohistochemistry revealed abnormal proliferation patterns in mutant fish.

CONCLUSIONS

The study suggests that ezrin may be involved in the enucleation and differentiation of lens epithelial cells.