Combining deep sequencing, proteomics, phosphoproteomics, and functional screens to discover novel regulators of sphingolipid homeostasis

Journal article

Sphingolipids (SLs) are essential components of cell membranes and are broad-range bioactive signaling molecules. SL levels must be tightly regulated as imbalances affect cellular function and contribute to pathologies ranging from neurodegenerative and metabolic disorders to cancer and aging. Deciphering how SL homeostasis is maintained and uncovering new regulators is required for understanding lipid biology and for identifying new targets for therapeutic interventions. Here we combine omics technologies to identify the changes of the transcriptome, proteome, and phosphoproteome in the yeast Saccharomyces cerevisiae upon SL depletion induced by myriocin. Surprisingly, while SL depletion triggers important changes in the expression of regulatory proteins involved in SL homeostasis, the most dramatic regulation occurs at the level of the phosphoproteome, suggesting that maintaining SL homeostasis demands rapid responses. To discover which of the phosphoproteomic changes are required for the cell's first-line response to SL depletion, we overlaid our omics results with systematic growth screens for genes required during growth in myriocin. By following the rate of SL biosynthesis in those candidates that are both affecting growth and are phosphorylated in response to the drug, we uncovered Atg9, Stp4, and Gvp36 as putative new regulators of SL homeostasis.

Authors: Lebesgue, N; Megyeri, M; Cristobal, A; Scholten, A; Chuartzman, S

• Publication status: Published
• Peer review status: Peer reviewed
• Publisher: American Chemical Society
• Journal: Journal of Proteome Research
• Volume: 16
• Issue: 2
• Pages: 571-582
• Publication date: 2016-11-14
• Acceptance date: 2016-11-14
• DOI: 10.1021/acs.jproteome.6b00691
• EISSN: 1535-3907
• ISSN: 1535-3893
• Pmid: 28152593
• Language: English
• Keywords: monosaccharide transport proteins; antifungal agents; sphingolipid metabolism; homeostasis; gene expression regulation, fungal; phosphoproteins; Saccharomyces cerevisiae proteins; Saccharomyces cerevisiae; aspartic acid endopeptidases; fatty acids, monounsaturated; sphingolipids; myriocin; high-throughput nucleotide sequencing; phosphorylation; label-free quantification; mass spectrometry; autophagy-related proteins; signal transduction; gene expression profiling; proteomics; membrane proteins