| Literature DB >> 32857977 |
Noemi Jiménez-Rojo1, Manuel D Leonetti2, Valeria Zoni3, Adai Colom1, Suihan Feng1, Namrata R Iyengar4, Stefan Matile5, Aurélien Roux1, Stefano Vanni3, Jonathan S Weissman2, Howard Riezman6.
Abstract
Sphingolipids play important roles in physiology and cell biology, but a systematic examination of their functions is lacking. We performed a genome-wide CRISPRi screen in sphingolipid-depleted human cells and identified hypersensitive mutants in genes of membrane trafficking and lipid biosynthesis, including ether lipid synthesis. Systematic lipidomic analysis showed a coordinate regulation of ether lipids with sphingolipids, suggesting an adaptation and functional compensation. Biophysical experiments on model membranes show common properties of these structurally diverse lipids that also share a known function as glycosylphosphatidylinositol (GPI) anchors in different kingdoms of life. Molecular dynamics simulations show a selective enrichment of ether phosphatidylcholine around p24 proteins, which are receptors for the export of GPI-anchored proteins and have been shown to bind a specific sphingomyelin species. Our results support a model of convergent evolution of proteins and lipids, based on their physico-chemical properties, to regulate GPI-anchored protein transport and maintain homeostasis in the early secretory pathway.Entities:
Keywords: CRISPR Cas9 screen; Ether lipids; Glycosylphosphatidylinositol (GPI)-anchored proteins; early secretory pathway; lipid homeostasis; sphingolipids; systematic lipidomics
Year: 2020 PMID: 32857977 DOI: 10.1016/j.cub.2020.07.059
Source DB: PubMed Journal: Curr Biol ISSN: 0960-9822 Impact factor: 10.834