1. Academic Validation
  2. Vps13-like proteins provide phosphatidylethanolamine for GPI anchor synthesis in the ER

Vps13-like proteins provide phosphatidylethanolamine for GPI anchor synthesis in the ER

  • J Cell Biol. 2022 Mar 7;221(3):e202111095. doi: 10.1083/jcb.202111095.
Alexandre Toulmay 1 Fawn B Whittle 1 Jerry Yang 1 Xiaofei Bai 2 Jessica Diarra 1 Subhrajit Banerjee 1 Tim P Levine 3 Andy Golden 2 William A Prinz 1
Affiliations

Affiliations

  • 1 Laboratory of Cell and Molecular Biology, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, MD.
  • 2 Laboratory of Biochemistry and Genetics, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, MD.
  • 3 University College London, Institute of Ophthalmology, London, UK.
Abstract

Glycosylphosphatidylinositol (GPI) is a glycolipid membrane anchor found on surface proteins in all eukaryotes. It is synthesized in the ER membrane. Each GPI anchor requires three molecules of ethanolamine phosphate (P-Etn), which are derived from phosphatidylethanolamine (PE). We found that efficient GPI anchor synthesis in Saccharomyces cerevisiae requires Csf1; cells lacking Csf1 accumulate GPI precursors lacking P-Etn. Structure predictions suggest Csf1 is a tube-forming lipid transport protein like Vps13. Csf1 is found at contact sites between the ER and other organelles. It interacts with the ER protein Mcd4, an Enzyme that adds P-Etn to nascent GPI anchors, suggesting Csf1 channels PE to Mcd4 in the ER at contact sites to support GPI anchor biosynthesis. CSF1 has orthologues in Caenorhabditis elegans (lpd-3) and humans (KIAA1109/TWEEK); mutations in KIAA1109 cause the autosomal recessive neurodevelopmental disorder Alkuraya-Kučinskas syndrome. Knockout of lpd-3 and knockdown of KIAA1109 reduced GPI-anchored proteins on the surface of cells, suggesting Csf1 orthologues in human cells support GPI anchor biosynthesis.

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