Rhodopsin activation causes retinal degeneration in Drosophila rdgC mutant

Neuron. 1990 Jun;4(6):883-90. doi: 10.1016/0896-6273(90)90141-2.

Abstract

Drosophila rdgC (retinal degeneration-C) mutants show normal retinal morphology and photoreceptor physiology at young ages. Dark-reared rdgC flies retain this wild-type phenotype, but light-reared mutants undergo retinal degeneration. rdgC photoreceptors with low levels of rhodopsin as a result of vitamin A deprivation or a mutant rhodopsin (ninaE) gene fail to show rdgC-induced degeneration even after prolonged light treatment, demonstrating that degeneration occurs as a result of light stimulation of rhodopsin. Analysis of norpA; rdgC flies shows that the norpA-encoded phospholipase C, the target enzyme of the G protein activated by rhodopsin, is not required for rdgC-induced degeneration. Thus the rdgC+ gene product is required to prevent retinal degeneration that results from a previously unrecognized consequence of rhodopsin stimulation.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Aging
  • Animals
  • Chromosome Mapping
  • Drosophila / genetics*
  • Drosophila / physiology
  • Electrophysiology / methods
  • Light
  • Microscopy, Electron
  • Mutation*
  • Phenotype
  • Photoreceptor Cells / growth & development
  • Photoreceptor Cells / physiology*
  • Photoreceptor Cells / ultrastructure
  • Retinal Degeneration*
  • Retinal Pigments / physiology*
  • Rhodopsin / physiology*
  • Type C Phospholipases / metabolism

Substances

  • Retinal Pigments
  • Rhodopsin
  • Type C Phospholipases