Crumbs, the Drosophila homologue of human CRB1/RP12, is essential for photoreceptor morphogenesis

Nature. 2002 Mar 14;416(6877):143-9. doi: 10.1038/nature721. Epub 2002 Feb 17.

Abstract

The apical transmembrane protein Crumbs is a central regulator of epithelial apical-basal polarity in Drosophila. Loss-of-function mutations in the human homologue of Crumbs, CRB1 (RP12), cause recessive retinal dystrophies, including retinitis pigmentosa. Here we show that Crumbs and CRB1 localize to corresponding subdomains of the photoreceptor apical plasma membrane: the stalk of the Drosophila photoreceptor and the inner segment of mammalian photoreceptors. These subdomains support the morphogenesis and orientation of the photosensitive membrane organelles: rhabdomeres and outer segments, respectively. Drosophila Crumbs is required to maintain zonula adherens integrity during the rapid apical membrane expansion that builds the rhabdomere. Crumbs also regulates stalk development by stabilizing the membrane-associated spectrin cytoskeleton, a function mechanistically distinct from its role in epithelial apical-basal polarity. We propose that Crumbs is a central component of a molecular scaffold that controls zonula adherens assembly and defines the stalk as an apical membrane subdomain. Defects in such scaffolds may contribute to human CRB1-related retinal dystrophies.

Publication types

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

MeSH terms

  • Adherens Junctions / chemistry
  • Adherens Junctions / metabolism
  • Adherens Junctions / ultrastructure
  • Animals
  • Cell Membrane / metabolism
  • Cell Polarity
  • Cytoskeleton / metabolism
  • Drosophila Proteins / genetics
  • Drosophila Proteins / metabolism*
  • Drosophila melanogaster / cytology
  • Drosophila melanogaster / embryology*
  • Drosophila melanogaster / genetics
  • Drosophila melanogaster / ultrastructure
  • Eye Proteins*
  • Humans
  • Membrane Proteins* / genetics
  • Membrane Proteins* / metabolism*
  • Mice
  • Morphogenesis
  • Mutation / genetics
  • Nerve Tissue Proteins*
  • Phenotype
  • Photoreceptor Cells, Invertebrate / cytology*
  • Photoreceptor Cells, Invertebrate / embryology*
  • Photoreceptor Cells, Invertebrate / metabolism
  • Photoreceptor Cells, Invertebrate / ultrastructure
  • Protein Binding
  • Retina / cytology
  • Retina / embryology
  • Retina / metabolism
  • Retina / ultrastructure
  • Sequence Homology*
  • Spectrin / metabolism

Substances

  • CRB1 protein, human
  • Drosophila Proteins
  • Eye Proteins
  • Membrane Proteins
  • Nerve Tissue Proteins
  • crb protein, Drosophila
  • Spectrin