A <i>Saccharomyces cerevisiae</i> Genome-Wide Mutant Screen for Altered Sensitivity to K1 Killer Toxin

Nicolas Pagé(McGill University), Manon Gérard‐Vincent(McGill University), P Ménard(McGill University), M. Beaulieu(McGill University), Masayuki Azuma(McGill University), Gerrit J.P. Dijkgraaf(McGill University), Huijuan Li(McGill University), José Marcoux(McGill University), Thuy N. Nguyen(McGill University), Tim Dowse(McGill University), Anne‐Marie Sdicu(McGill University), Howard Bussey(McGill University)
Genetics
March 1, 2003
Cited by 167Open Access
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Abstract

Using the set of Saccharomyces cerevisiae mutants individually deleted for 5718 yeast genes, we screened for altered sensitivity to the antifungal protein, K1 killer toxin, that binds to a cell wall beta-glucan receptor and subsequently forms lethal pores in the plasma membrane. Mutations in 268 genes, including 42 in genes of unknown function, had a phenotype, often mild, with 186 showing resistance and 82 hypersensitivity compared to wild type. Only 15 of these genes were previously known to cause a toxin phenotype when mutated. Mutants for 144 genes were analyzed for alkali-soluble beta-glucan levels; 63 showed alterations. Further, mutants for 118 genes with altered toxin sensitivity were screened for SDS, hygromycin B, and calcofluor white sensitivity as indicators of cell surface defects; 88 showed some additional defect. There is a markedly nonrandom functional distribution of the mutants. Many genes affect specific areas of cellular activity, including cell wall glucan and mannoprotein synthesis, secretory pathway trafficking, lipid and sterol biosynthesis, and cell surface signal transduction, and offer new insights into these processes and their integration.


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