In Saccharomyces cerevisiae, replication stress induced by hydroxyurea (HU) and methyl methanesulfonate (MMS) activates DNA integrity checkpoints; in checkpoint-defective yeast strains, HU treatment also induces morphological aberrations. We find that the sphingolipid pathway gene ISC1, the product of which catalyzes the generation of bioactive ceramides from complex sphingolipids, plays a novel role in determining cellular morphology following HU/MMS treatment. HU-treated isc1Δ cells display morphological aberrations, cell-wall defects, and defects in actin depolymerization. Swe1, a morphogenesis checkpoint regulator, and the cell cycle regulator Cdk1 play key roles in these morphological defects of isc1Δ cells. A genetic approach reveals that ISC1 interacts with other checkpoint proteins to control cell morphology. That is, yeast carrying deletions of both ISC1 and a replication checkpoint mediator gene including MRC1, TOF1, or CSM3 display basal morphological defects, which increase following HU treatment. Interestingly, strains with deletions of both ISC1 and the DNA damage checkpoint mediator gene RAD9 display reduced morphological aberrations irrespective of HU treatment, suggesting a role for RAD9 in determining the morphology of isc1Δ cells. Mechanistically, the checkpoint regulator Rad53 partially influences isc1Δ cell morphology in a dosage-dependent manner.
Pubmed ID: 21840863 RIS Download
Mesh terms: Actins | Blotting, Western | CDC28 Protein Kinase, S cerevisiae | Cell Cycle Proteins | Cell Wall | Chitin | DNA Damage | DNA Repair | DNA Replication | DNA-Binding Proteins | Hydroxyurea | Methyl Methanesulfonate | Microscopy, Fluorescence | Mutagens | Mutation | Nucleic Acid Synthesis Inhibitors | Protein-Tyrosine Kinases | Saccharomyces cerevisiae | Saccharomyces cerevisiae Proteins | Sphingolipids | Type C Phospholipases
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