Cargo can modulate COPII vesicle formation from the endoplasmic reticulum

J Biol Chem. 1999 Feb 12;274(7):4389-99. doi: 10.1074/jbc.274.7.4389.

Abstract

The COPII coat complex found on endoplasmic reticulum (ER)-derived vesicles plays a critical role in cargo selection. We now address the potential role of biosynthetic cargo in modulating COPII coat assembly and vesicle budding. The ER accumulation of vesicular stomatitis glycoprotein (VSV-G), a transmembrane protein, or the soluble PiZ variant of alpha1-antitrypsin, reduced levels of general COPII vesicle formation in vivo. Consistent with this result, conditions that prevent the export of VSV-G from the ER led to a significant inhibition of general COPII vesicle budding from ER microsomes and the export of an endogenous recycling protein p58 in vitro. In contrast, synchronized export of VSV-G stimulated COPII vesicle budding both in vivo and in vitro. Under conditions where VSV-G is retained in the ER, we find that it can to be recovered in pre-budding complexes containing COPII components. These results suggest that the export of biosynthetic cargo is integrated with ER functions involved in protein folding and oligomerization. The ability of biosynthetic cargo to prevent or enhance ER export suggests that interactions of cargo with the COPII machinery contribute to the formation of vesicles budding from the ER.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Biological Transport
  • Carrier Proteins / metabolism*
  • Cell Line
  • Endoplasmic Reticulum / metabolism*
  • GTP-Binding Proteins / metabolism
  • Kidney / metabolism
  • Kidney / ultrastructure
  • Membrane Glycoproteins*
  • Microscopy, Electron
  • Monomeric GTP-Binding Proteins*
  • Phosphoproteins / metabolism*
  • Protein Folding
  • Proteins / metabolism
  • Rats
  • Saccharomyces cerevisiae Proteins*
  • Temperature
  • Vesicular Transport Proteins
  • Viral Envelope Proteins / metabolism*
  • alpha 1-Antitrypsin / metabolism*

Substances

  • A1PiZ protein, S cerevisiae
  • Carrier Proteins
  • G protein, vesicular stomatitis virus
  • Membrane Glycoproteins
  • Phosphoproteins
  • Proteins
  • SEC31 protein, S cerevisiae
  • Saccharomyces cerevisiae Proteins
  • Sec23a protein, rat
  • Vesicular Transport Proteins
  • Viral Envelope Proteins
  • alpha 1-Antitrypsin
  • GTP-Binding Proteins
  • Monomeric GTP-Binding Proteins
  • SAR1 protein, S cerevisiae