Hibris, a Drosophila nephrin homolog, is required for presenilin-mediated Notch and APP-like cleavages

Dev Cell. 2012 Jul 17;23(1):82-96. doi: 10.1016/j.devcel.2012.04.021.

Abstract

Drosophila Hibris (Hbs), a member of the Nephrin Immunoglobulin Super Family, has been implicated in myogenesis and eye patterning. Here, we uncover a role of Hbs in Notch (N) signaling and γ-secretase processing. Loss of hbs results in classical N-signaling-associated phenotypes in Drosophila, including eye patterning, wing margin, and sensory organ specification defects. In particular, hbs mutant larvae display altered γ-secretase-dependent Notch proteolytic processing. Hbs also interacts molecularly and genetically with Presenilin (Psn) and other components of the γ-secretase complex. This Hbs function appears conserved, as mammalian Nephrin also promotes N signaling in mammalian cells. Our data suggest that Hbs is required for Psn maturation. Consistent with its role in Psn processing, Hbs genetically interacts with the Drosophila β-amyloid protein precursor-like (Appl) protein, the homolog of mammalian APP, the cleavage of which is associated with Alzheimer's disease. Thus, Hbs/Nephrin appear to share a general requirement in Psn/γ-secretase regulation and associated processes.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Amyloid beta-Protein Precursor / genetics
  • Amyloid beta-Protein Precursor / metabolism*
  • Animals
  • Drosophila Proteins / genetics
  • Drosophila Proteins / metabolism*
  • Drosophila Proteins / physiology*
  • Drosophila melanogaster / embryology
  • Drosophila melanogaster / genetics
  • Drosophila melanogaster / metabolism*
  • Genetic Association Studies
  • Membrane Proteins / genetics
  • Membrane Proteins / metabolism
  • Membrane Proteins / physiology*
  • Multigene Family / physiology
  • Multiprotein Complexes / genetics
  • Multiprotein Complexes / metabolism
  • Mutagenesis / physiology
  • Pedigree
  • Presenilins / genetics
  • Presenilins / physiology*
  • Receptors, Notch / genetics
  • Receptors, Notch / metabolism*

Substances

  • Amyloid beta-Protein Precursor
  • Drosophila Proteins
  • Membrane Proteins
  • Multiprotein Complexes
  • N protein, Drosophila
  • Presenilins
  • Psn protein, Drosophila
  • Receptors, Notch
  • hbs protein, Drosophila
  • nephrin