Does Rft1 flip an N-glycan lipid precursor?

Nature. 2008 Jul 31;454(7204):E3-4; discussion E4-5. doi: 10.1038/nature07165.

Abstract

Protein N-glycosylation requires flipping of the glycolipid Man(5)GlcNAc(2)-diphosphate dolichol (Man(5)GlcNAc(2)-PP-Dol) across the endoplasmic reticulum (ER). Helenius et al. report genetic evidence suggesting that Rft1, an essential ER membrane protein in yeast, is required directly to translocate Man(5)GlcNAc(2)-PP-Dol. We now show that a specific ER protein(s), but not Rft1, is required to flip Man(5)GlcNAc(2)-PP-Dol in reconstituted vesicles. Rft1 may have a critical accessory role in translocating Man(5)GlcNAc(2)-PP-Dol in vivo, but the Man(5)GlcNAc(2)-PP-Dol flippase itself remains to be identified.

Publication types

  • Comment

MeSH terms

  • Dolichols / analogs & derivatives*
  • Dolichols / metabolism
  • Mannans / metabolism*
  • Membrane Glycoproteins / metabolism*
  • Membrane Transport Proteins
  • Phospholipid Transfer Proteins / metabolism*
  • Reproducibility of Results
  • Saccharomyces cerevisiae / cytology
  • Saccharomyces cerevisiae / metabolism*
  • Saccharomyces cerevisiae Proteins / metabolism*

Substances

  • Dolichols
  • Man(6)GlcNAc(2)-PP-dolichol
  • Mannans
  • Membrane Glycoproteins
  • Membrane Transport Proteins
  • Phospholipid Transfer Proteins
  • RFT1 protein, S cerevisiae
  • Saccharomyces cerevisiae Proteins