Plasma membrane--endoplasmic reticulum contact sites regulate phosphatidylcholine synthesis

EMBO Rep. 2013 May;14(5):434-40. doi: 10.1038/embor.2013.36. Epub 2013 Mar 22.

Abstract

Synthesis of phospholipids, sterols and sphingolipids is thought to occur at contact sites between the endoplasmic reticulum (ER) and other organelles because many lipid-synthesizing enzymes are enriched in these contacts. In only a few cases have the enzymes been localized to contacts in vivo and in no instances have the contacts been demonstrated to be required for enzyme function. Here, we show that plasma membrane (PM)--ER contact sites in yeast are required for phosphatidylcholine synthesis and regulate the activity of the phosphatidylethanolamine N-methyltransferase enzyme, Opi3. Opi3 activity requires Osh3, which localizes to PM-ER contacts where it might facilitate in trans catalysis by Opi3. Thus, membrane contact sites provide a structural mechanism to regulate lipid synthesis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Membrane / metabolism*
  • Cell Membrane / ultrastructure
  • Endoplasmic Reticulum / metabolism*
  • Endoplasmic Reticulum / ultrastructure
  • Gene Knockout Techniques
  • Membrane Proteins / genetics
  • Membrane Proteins / metabolism
  • Phosphatidate Phosphatase / metabolism
  • Phosphatidylcholines / biosynthesis*
  • Phosphoric Monoester Hydrolases / metabolism
  • Saccharomyces cerevisiae / genetics
  • Saccharomyces cerevisiae / metabolism*
  • Saccharomyces cerevisiae / ultrastructure
  • Saccharomyces cerevisiae Proteins / genetics
  • Saccharomyces cerevisiae Proteins / metabolism

Substances

  • Ice2 protein, S cerevisiae
  • Membrane Proteins
  • Phosphatidylcholines
  • Saccharomyces cerevisiae Proteins
  • Scs2 protein, S cerevisiae
  • SAC1 protein, S cerevisiae
  • Phosphoric Monoester Hydrolases
  • PAH1 protein, S cerevisiae
  • Phosphatidate Phosphatase