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Vps13-like proteins provide phosphatidylethanolamine for GPI anchor synthesis in the ER
Author(s) -
Alexandre Toulmay,
Fawn B. Whittle,
Jerry Yang,
Xiaofei Bai,
Jessica Diarra,
Subhrajit Banerjee,
Tim P. Levine,
Andy Golden,
William A. Prinz
Publication year - 2022
Publication title -
the journal of cell biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.414
H-Index - 380
eISSN - 1540-8140
pISSN - 0021-9525
DOI - 10.1083/jcb.202111095
Subject(s) - phosphatidylethanolamine , organelle , caenorhabditis elegans , microbiology and biotechnology , glycolipid , chemistry , biosynthesis , membrane protein , saccharomyces cerevisiae , biochemistry , biology , gene , membrane , phospholipid , phosphatidylcholine
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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