A link between ER tethering and COP-I vesicle uncoating

Dev Cell. 2009 Sep;17(3):403-16. doi: 10.1016/j.devcel.2009.07.012.

Abstract

The yeast Dsl1p vesicle tethering complex, comprising the three subunits Dsl1p, Dsl3p, and Tip20p, is stably associated with three endoplasmic reticulum-localized Q-SNAREs and is believed to play a central role in the tethering and fusion of Golgi-derived COP-I transport vesicles. Dsl1p also interacts directly with COP-I subunits. We now show that binding of Dsl1p to COP-I subunits involves binding sites identical to those involved in interactions between COP-I subunits that stabilize the COP-I coat. Cells with defects in Dsl/SNARE complex function show massive accumulation of COP-I-coated vesicles in a cluster to which COP-II coat proteins are also recruited. Our results suggest that binding of Dsl/SNARE complex to the COP-I coat complex serves two functions: to mediate vesicle tethering and to assist the uncoating process by blocking domains in COP-I that drive repolymerization and the formation of large COP-I aggregates.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Binding Sites
  • Coat Protein Complex I / metabolism*
  • Down-Regulation
  • Endoplasmic Reticulum / metabolism*
  • Glutathione Transferase / metabolism
  • Microscopy, Confocal / methods
  • Microscopy, Fluorescence / methods
  • Models, Biological
  • Models, Genetic
  • Mutation
  • Phenotype
  • Plasmids / metabolism
  • Saccharomyces cerevisiae / physiology*
  • Saccharomyces cerevisiae Proteins / metabolism*

Substances

  • Coat Protein Complex I
  • DSL1 protein, S cerevisiae
  • Saccharomyces cerevisiae Proteins
  • Glutathione Transferase