The transitional ER localization mechanism of Pichia pastoris Sec12

Dev Cell. 2004 May;6(5):649-59. doi: 10.1016/s1534-5807(04)00129-7.

Abstract

COPII vesicles assemble at ER subdomains called transitional ER (tER) sites, but the mechanism that generates tER sites is unknown. To study tER biogenesis, we analyzed the transmembrane protein Sec12, which initiates COPII vesicle formation. Sec12 is concentrated at discrete tER sites in the budding yeast Pichia pastoris. We find that P. pastoris Sec12 exchanges rapidly between tER sites and the general ER. The tER localization of Sec12 is saturable and is mediated by interaction of the Sec12 cytosolic domain with a partner component. This interaction apparently requires oligomerization of the Sec12 lumenal domain. Redistribution of P. pastoris Sec12 to the general ER does not perturb the localization of downstream tER components, suggesting that Sec12 and other COPII proteins associate with a tER scaffold. These results provide evidence that tER sites form by a network of dynamic associations at the cytosolic face of the ER.

Publication types

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

MeSH terms

  • COP-Coated Vesicles / metabolism*
  • Cytosol / metabolism
  • Cytosol / ultrastructure
  • Endoplasmic Reticulum / metabolism*
  • Endoplasmic Reticulum / ultrastructure
  • Golgi Apparatus / metabolism
  • Golgi Apparatus / ultrastructure
  • Guanine Nucleotide Exchange Factors
  • Membrane Glycoproteins / genetics
  • Membrane Glycoproteins / metabolism
  • Membrane Proteins / genetics
  • Membrane Proteins / metabolism*
  • Microscopy, Electron
  • Pichia / metabolism*
  • Pichia / ultrastructure
  • Protein Structure, Tertiary / physiology
  • Protein Transport / physiology*
  • Saccharomyces cerevisiae Proteins / genetics
  • Saccharomyces cerevisiae Proteins / metabolism

Substances

  • Guanine Nucleotide Exchange Factors
  • Membrane Glycoproteins
  • Membrane Proteins
  • SEC12 protein, S cerevisiae
  • Saccharomyces cerevisiae Proteins