Analysis of β-1,3-Glucan Assembly in Saccharomyces cerevisiae Using a Synthetic Interaction Network and Altered Sensitivity to Caspofungin
Abstract
Large-scale screening of genetic and chemical-genetic interactions was used to examine the assembly and regulation of beta-1,3-glucan in Saccharomyces cerevisiae. Using the set of deletion mutants in approximately 4600 nonessential genes, we scored synthetic interactions with genes encoding subunits of the beta-1,3-glucan synthase (FKS1, FKS2), the glucan synthesis regulator (SMI1/KNR4), and a beta-1,3-glucanosyltransferase (GAS1). In the resulting network, FKS1, FKS2, GAS1, and SMI1 are connected to 135 genes in 195 interactions, with 26 of these genes also interacting with CHS3 encoding chitin synthase III. A network core of 51 genes is multiply connected with 112 interactions. Thirty-two of these core genes are known to be involved in cell wall assembly and polarized growth, and 8 genes of unknown function are candidates for involvement in these processes. In parallel, we screened the yeast deletion mutant collection for altered sensitivity to the glucan synthase inhibitor, caspofungin. Deletions in 52 genes led to caspofungin hypersensitivity and those in 39 genes to resistance. Integration of the glucan interaction network with the caspofungin data indicates an overlapping set of genes involved in FKS2 regulation, compensatory chitin synthesis, protein mannosylation, and the PKC1-dependent cell integrity pathway.
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Our identified genes are consistent with functional categories of chemical-genetic interactors of caspofungin identified in S. cerevisiae.
“Consistent with functional categories of chemical-genetic interactors of caspofungin identified in S. cerevisiae (Lesage et al., 2004”
From Functional Genomic Screening Reveals Core Modulators of Echinocandin Stress Responses in Candida albicans (2018) · cites this paper as Lesage et al., 2004
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References 53 · Cited by 166
- Authors
- Lesage, G., Sdicu, A.-M., Ménard, P., Shapiro, J., Hussein, S., & Bussey, H.
- Affiliations
- McGill University (CA)
- Department of Biology, McGill University, Montreal, Québec H3A 1B1, Canada
- Corresponding author
- Bussey, Howard
- ORCID
- Ménard, Patrice
- Venue
- Genetics
- Publisher
- Oxford University Press (OUP)
- Published
- 2004-05-01
- Volume
- 167
- Issue
- 1
- Pages
- 35-49
- ISSN
- 0016-6731 (ISSN-L)
- 1943-2631
- OpenAlex
- W2155687518
- Cited by
- 166
- References
- 53
- Citations by year
- 2026: 4 · 2025: 3 · 2024: 3 · 2022: 5 · 2021: 3 · 2020: 2 · 2019: 5 · 2018: 8 · 2017: 5 · 2016: 7 · 2015: 6 · 2014: 9 · 2013: 9 · 2012: 11
- FWCI
- 4.85
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- academic.oup.com/journals/pages/open_access/funder_policies/chorus/standard_publication_model (vor)
- Locations
- Genetics (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Fungal and yeast genetics research
- Health Sciences › Medicine › Infectious Diseases › Antifungal resistance and susceptibility
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Yeasts and Rust Fungi Studies
- Keywords
- β-1,3-glucan, cell wall assembly, beta-1,3-glucan synthase, FKS1, FKS2, GAS1, CHS3, synthetic genetic interactions, deletion mutants, cell integrity pathway, PKC1, polarized growth, Saccharomyces cerevisiae
- MeSH terms
- Caspofungin, Antifungal Agents, Biochemistry, Biological Transport, Cell Cycle, Cell Survival, Cell Wall, Chitin, Cytoskeleton, Dose-Response Relationship, Drug, Genes, Fungal, Genotype, Glucans, Glucosyltransferases, Haploidy, Ions, Membrane Glycoproteins, Membrane Proteins, Models, Biological, Mutation, Peptides, Cyclic, Phenotype, Protein Binding, Proteins, Saccharomyces cerevisiae, Time Factors, Transcription Factors, Transcription, Genetic, Signal Transduction, Gene Deletion, Drug Resistance, Multiple, Oligonucleotide Array Sequence Analysis, Drug Resistance, Fungal, Ubiquitin, Saccharomyces cerevisiae Proteins, beta-Glucans, Echinocandins, Lipopeptides
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