Hedgehog signal transduction proteins: contacts of the Fused kinase and Ci transcription factor with the kinesin-related protein Costal2

BMC Dev Biol. 2002 Mar 19:2:4. doi: 10.1186/1471-213x-2-4.

Abstract

Background: Hedgehog signaling proteins play important roles in development by controlling growth and patterning in various animals including Drosophila and mammals. Hedgehog signaling triggers changes in responsive cells through a novel transduction mechanism that ultimately controls the transcription of specific target genes via the activity of zinc finger transcription factors of the Cubitus interruptus/GLI family. In flies, key Hedgehog signal transduction components have been identified including the kinesin-related protein Costal2, the serinethreonine kinase Fused, and the PEST-containing protein Suppressor of Fused. These proteins control Cubitus interruptus cleavage, nucleo-cytoplasmic localization and activation. In fly embryos, Costal2, Fused, Suppressor of Fused and Cubitus interruptus are associated in at least one cytoplasmic complex, which interacts with the microtubules in a Hedgehog-dependent manner.

Results: Here we identified and mapped direct interactions between Cos2, Fu, and Ci using an in vitro affinity assay and the yeast two-hybrid system.

Conclusions: Our results provide new insights into the possible mechanism of the cytosolic steps of Hedgehog transduction.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Binding Sites
  • DNA-Binding Proteins / metabolism*
  • DNA-Binding Proteins / physiology
  • Drosophila Proteins / metabolism*
  • Drosophila Proteins / physiology*
  • Glutathione Transferase / metabolism
  • Hedgehog Proteins
  • Kinesins / metabolism*
  • Kinesins / physiology
  • Peptide Fragments / metabolism
  • Peptide Fragments / physiology
  • Protein Interaction Mapping / methods*
  • Protein Serine-Threonine Kinases / metabolism*
  • Protein Serine-Threonine Kinases / physiology
  • Recombinant Fusion Proteins / metabolism
  • Signal Transduction / physiology*
  • Transcription Factors / metabolism
  • Transcription Factors / physiology
  • Two-Hybrid System Techniques
  • Zinc Fingers / physiology

Substances

  • DNA-Binding Proteins
  • Drosophila Proteins
  • Hedgehog Proteins
  • Peptide Fragments
  • Recombinant Fusion Proteins
  • Transcription Factors
  • ci protein, Drosophila
  • cos protein, Drosophila
  • hh protein, Drosophila
  • Glutathione Transferase
  • fu protein, Drosophila
  • Protein Serine-Threonine Kinases
  • Kinesins