Cullin-5 plays multiple roles in cell fate specification and synapse formation during Drosophila development

Dev Dyn. 2005 Mar;232(3):865-75. doi: 10.1002/dvdy.20322.

Abstract

We describe a developmental analysis of Drosophila Cullin-5 (Cul-5) identified from the genome sequence on the basis of its high degree of homology to vertebrate and worm sequences. The gene is expressed in a restricted manner in ectodermal cells throughout development suggesting pleiotropic functions. We decided to examine the phenotypes of Cul-5 aberrations in two well-studied developmental systems: the neuromuscular junction (NMJ) and the developing sensory organ. Alteration of Cul-5 levels in motoneurons results in an increase in bouton number at the NMJ. The cells of a sensory organ on the adult notum arise from a single progenitor cell by regulated cell division. Aberrations in Cul-5 affect different steps in the lineage consistent with a role in cell fate determination, proliferation, and death. Such phenotypes highlight the multiple cellular processes in which Cul-5 can participate.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Cell Division
  • Cullin Proteins / chemistry
  • Cullin Proteins / genetics
  • Cullin Proteins / metabolism*
  • Cullin Proteins / ultrastructure
  • Drosophila / embryology*
  • Drosophila / genetics
  • Drosophila / growth & development
  • Drosophila / ultrastructure
  • Drosophila Proteins / chemistry
  • Drosophila Proteins / genetics
  • Drosophila Proteins / metabolism*
  • Drosophila Proteins / ultrastructure
  • Embryo, Nonmammalian
  • Gene Expression
  • Gene Expression Regulation
  • Genes, Insect
  • Larva
  • Metamorphosis, Biological
  • Molecular Sequence Data
  • Mutation
  • Neuromuscular Junction / cytology
  • Neuromuscular Junction / embryology*
  • Neuromuscular Junction / ultrastructure
  • Neurons, Afferent / cytology*
  • Neurons, Afferent / ultrastructure
  • Organogenesis
  • Pupa
  • RNA, Messenger / metabolism
  • Sequence Homology, Amino Acid
  • Synapses / metabolism*
  • Synapses / ultrastructure

Substances

  • Cullin Proteins
  • Drosophila Proteins
  • RNA, Messenger