Cytotoxicity of 1-deoxysphingolipid unraveled by genome-wide genetic screens and lipidomics in Saccharomyces cerevisiae.

Abstract

Hereditary sensory and autonomic neuropathy (HSAN) types IA and IC (IA/C) are caused by elevated levels of an atypical class of lipid named 1-deoxysphingolipid (DoxSL). How elevated levels of DoxSL perturb the physiology of the cell and how the perturbations lead to HSAN IA/C are largely unknown. In this study, we show that C26-1-deoxydihydroceramide (C26-DoxDHCer) is highly toxic to the cell, while C16- and C18-DoxDHCer are less toxic. Genome-wide genetic screens and lipidomics revealed the dynamics of DoxSL accumulation and DoxSL species responsible for the toxicity over the course of DoxSL accumulation. Moreover, we show that disruption of F-actin organization, alteration of mitochondrial shape, and accumulation of hydrophobic bodies by DoxSL are not sufficient to cause complete cellular failure. We found that cell death coincides with collapsed ER membrane, although we cannot rule out other possible causes of cell death. Thus, we have unraveled key principles of DoxSL cytotoxicity that may help to explain the clinical features of HSAN IA/C.

• Authors: A Galih Haribowo, J Thomas Hannich, Agnès H Michel, Márton Megyeri, Maya Schuldiner, Benoît Kornmann, Howard Riezman
• Journal: Molecular biology of the cell (Mol Biol Cell) Vol. 30 Issue 22 Pg. 2814-2826 (10 15 2019) ISSN: 1939-4586 [Electronic] United States
• PMID: 31509475 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• 1-deoxysphingolipid
• Actins
• Ceramides
• Lipids
• Saccharomyces cerevisiae Proteins
• Sphingolipids
• dihydroceramide

Topics

• Actins (metabolism)
• Ceramides (toxicity)
• Hereditary Sensory and Autonomic Neuropathies (metabolism, physiopathology)
• Lipid Metabolism
• Lipidomics
• Lipids
• Mitochondria (metabolism)
• Saccharomyces cerevisiae (metabolism)
• Saccharomyces cerevisiae Proteins (metabolism)
• Sphingolipids (genetics, metabolism)