Elevation of endogenous sphingolipid long-chain base phosphates kills Saccharomyces cerevisiae cells

Sphingolipid long-chain base phosphate (LCBPs) regulate cell proliferation, movement and differentiation in higher eukaryotes. To study the function of LCBPs in Saccharomyces cerevisiae, we inactivated LCBP breakdown pathways. Elimination of both the Dp11 lyase and the Lcb3 phosphatase pathways by gene deletion was lethal, indicating that these enzymes regulate LCBP levels to prevent accumulation. Lethality was prevented by eliminating the major LCB kinase, Lcb4p, which synthesizes LCBPs, but not by eliminating the minor LCB kinase, Lcb5p. These data imply that death results from an accumulation of LCBPs made by the Lcb4p kinase. By regulating Lcb4 kinase activity, we found that cell death correlates with LCBP accumulation and that C-18 dihydrosphingosine-1-P (DHS-P) and C-20 DHS-P are most likely the killing molecules. LCB levels were found to be most elevated in a strain lacking Lcb4 kinase, Dp11 lyase and Lcb3 phosphatase activity. Analysis of mutant strains suggests that the C-18 and C-20 species of LCBPs are preferentially degraded by the Lcb3 phosphate phosphatase, while the Dp11 lyase prefers C-16 DHS-P as a substrate. These and other data indicate the existence of an unknown mechanism(s) for regulating LCB levels. Our results demonstrate that LCBPs may be used in some circumstances to regulate yeast cell growth.