Coatomer interaction with di-lysine endoplasmic reticulum retention motifs

Science. 1994 Mar 18;263(5153):1629-31. doi: 10.1126/science.8128252.

Abstract

Although signals for retention in the endoplasmic reticulum (ER) have been identified in the cytoplasmic domain of various ER-resident type I transmembrane proteins, the mechanisms responsible for ER retention are still unknown. Yeast and mammalian ER retention motifs interacted specifically in cell lysates with the coatomer, a polypeptide complex implicated in membrane traffic. Mutations that affect the ER retention capacity of the motifs also abolished binding of the coatomer. These results suggest a role for the coatomer in the retrieval of transmembrane proteins to the ER in both yeast and mammals.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Biological Transport
  • Cell Line
  • Coatomer Protein
  • Endoplasmic Reticulum / metabolism*
  • Fungal Proteins / chemistry
  • Fungal Proteins / metabolism*
  • Golgi Apparatus / metabolism
  • Hexosyltransferases*
  • Lysine / chemistry
  • Lysine / metabolism*
  • Membrane Proteins / metabolism*
  • Molecular Sequence Data
  • Mutation
  • Recombinant Fusion Proteins / chemistry
  • Recombinant Fusion Proteins / metabolism
  • Transferases / chemistry
  • Transferases / metabolism*

Substances

  • Coatomer Protein
  • Fungal Proteins
  • Membrane Proteins
  • Recombinant Fusion Proteins
  • Transferases
  • Hexosyltransferases
  • dolichyl-diphosphooligosaccharide - protein glycotransferase
  • Lysine