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Transmembrane receptor DCC associates with protein synthesis machinery and regulates translation.

Extracellular signals regulate protein translation in many cell functions. A key advantage of control at the translational level is the opportunity to regulate protein synthesis within specific cellular subregions. However, little is known about mechanisms that may link extracellular cues to translation with spatial precision. Here, we show that a transmembrane receptor, DCC, forms a binding complex containing multiple translation components, including eukaryotic initiation factors, ribosomal large and small subunits, and monosomes. In neuronal axons and dendrites DCC colocalizes in particles with translation machinery, and newly synthesized protein. The extracellular ligand netrin promoted DCC-mediated translation and disassociation of translation components. The functional and physical association of a cell surface receptor with the translation machinery leads to a generalizable model for localization and extracellular regulation of protein synthesis, based on a transmembrane translation regulation complex.

Pubmed ID: 20434207


  • Tcherkezian J
  • Brittis PA
  • Thomas F
  • Roux PP
  • Flanagan JG



Publication Data

May 14, 2010

Associated Grants

  • Agency: NINDS NIH HHS, Id: P01 NS040043
  • Agency: NINDS NIH HHS, Id: P01 NS040043-100003
  • Agency: NEI NIH HHS, Id: R01 EY011559
  • Agency: NEI NIH HHS, Id: R01 EY011559-19
  • Agency: NICHD NIH HHS, Id: R37 HD029417
  • Agency: NICHD NIH HHS, Id: R37 HD029417-19
  • Agency: Canadian Institutes of Health Research, Id:

Mesh Terms

  • Amino Acid Motifs
  • Animals
  • Axons
  • Cells, Cultured
  • Chick Embryo
  • Dendrites
  • Hippocampus
  • Humans
  • Mice
  • Nerve Growth Factors
  • Neurons
  • Protein Biosynthesis
  • Protein Structure, Tertiary
  • Rats
  • Receptors, Cell Surface
  • Ribosomal Proteins
  • Ribosomes
  • Tumor Suppressor Proteins