Arrested differentiation and epithelial cell degeneration in zebrafish lens mutants

Dev Dyn. 2001 Dec;222(4):625-36. doi: 10.1002/dvdy.1217.

Abstract

In a chemical mutagenesis screen, we identified two zebrafish mutants that possessed small pupils. Genetic complementation revealed these two lines are due to mutations in different genes. The phenotypes of the two mutants were characterized using histologic, immunohistochemical, and tissue transplantation techniques. The arrested lens (arl) mutant exhibits a small eye and pupil phenotype at 48 hr postfertilization (hpf) and lacks any histologically identifiable lens structures by 5 days postfertilization (dpf). In contrast, the disrupted lens (dsl) mutants are phenotypically normal until 5 dpf, and then undergo lens disorganization and cell degeneration that is apparent by 7 dpf. Histology reveals the arl mutant terminates lens cell differentiation by 48 hpf, whereas the dsl lens exhibits a defective lens epithelial cell population at 5 dpf. Lens transplantation experiments demonstrate both mutations are autonomous to the lens tissue. Immunohistochemistry reveals the retinal cells may suffer subtle effects, possibly due to the lens abnormalities.

MeSH terms

  • Animals
  • Cell Death
  • Cell Differentiation
  • Embryo, Nonmammalian / cytology
  • Embryo, Nonmammalian / metabolism
  • Epithelial Cells / cytology*
  • Epithelial Cells / pathology*
  • Homeodomain Proteins / metabolism
  • Immunohistochemistry
  • Lens, Crystalline / embryology*
  • Lens, Crystalline / transplantation
  • Male
  • Mutation / physiology*
  • Phenotype
  • Retina / cytology
  • Retina / embryology
  • Tumor Suppressor Proteins
  • Zebrafish / embryology*

Substances

  • Homeodomain Proteins
  • Tumor Suppressor Proteins
  • prospero-related homeobox 1 protein