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A set of gene knockouts as a resource for global lipidomic changes

Aleksandra SpiegelMax Planck Institute of Molecular Cell Biology and Genetics, Pfotenhauerstrasse 108, 01307, Dresden, GermanyChris LauberLipotype GmbH, Tatzberg 47, 01307, Dresden, GermanyMandy BachmannMax Planck Institute of Molecular Cell Biology and Genetics, Pfotenhauerstrasse 108, 01307, Dresden, GermanyAnne‐Kristin HeningerMax Planck Institute of Molecular Cell Biology and Genetics, Pfotenhauerstrasse 108, 01307, Dresden, GermanyChristian KloseLipotype GmbH, Tatzberg 47, 01307, Dresden, GermanyKai SimonsLipotype GmbH, Tatzberg 47, 01307, Dresden, GermanyMihail SarovMax Planck Institute of Molecular Cell Biology and Genetics, Pfotenhauerstrasse 108, 01307, Dresden, GermanyMathias J. GerlLipotype GmbH, Tatzberg 47, 01307, Dresden, Germany. [email protected]
Scientific Reportsjournal2022en
ABI

Аннотация

Enzyme specificity in lipid metabolic pathways often remains unresolved at the lipid species level, which is needed to link lipidomic molecular phenotypes with their protein counterparts to construct functional pathway maps. We created lipidomic profiles of 23 gene knockouts in a proof-of-concept study based on a CRISPR/Cas9 knockout screen in mammalian cells. This results in a lipidomic resource across 24 lipid classes. We highlight lipid species phenotypes of multiple knockout cell lines compared to a control, created by targeting the human safe-harbor locus AAVS1 using up to 1228 lipid species and subspecies, charting lipid metabolism at the molecular level. Lipid species changes are found in all knockout cell lines, however, some are most apparent on the lipid class level (e.g., SGMS1 and CEPT1), while others are most apparent on the fatty acid level (e.g., DECR2 and ACOT7). We find lipidomic phenotypes to be reproducible across different clones of the same knockout and we observed similar phenotypes when two enzymes that catalyze subsequent steps of the long-chain fatty acid elongation cycle were targeted.

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