Analysis of β-1,3-glucan assembly in Saccharomyces cerevisiae using a synthetic interaction network and altered sensitivity to caspofungin

被引:128
作者
Lesage, G [1 ]
Sdicu, AM [1 ]
Ménard, P [1 ]
Shapiro, J [1 ]
Hussein, S [1 ]
Bussey, H [1 ]
机构
[1] McGill Univ, Dept Biol, Montreal, PQ H3A 1B1, Canada
关键词
D O I
10.1534/genetics.167.1.35
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
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 similar to4600 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.
引用
收藏
页码:35 / 49
页数:15
相关论文
共 52 条
  • [1] Genome-wide expression profiling of the response to polyene, pyrimidine, azole, and echinocandin antifungal agents in Saccharomyces cerevisiae
    Agarwal, AK
    Rogers, PD
    Baerson, SR
    Jacob, MR
    Barker, KS
    Cleary, JD
    Walker, LA
    Nagle, DG
    Clark, AM
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (37) : 34998 - 35015
  • [2] Hyperosmotic stress response and regulation of cell wall integrity in Saccharomyces cerevisiae share common functional aspects
    Alonso-Monge, R
    Real, E
    Wojda, I
    Bebelman, JP
    Mager, WH
    Siderius, M
    [J]. MOLECULAR MICROBIOLOGY, 2001, 41 (03) : 717 - 730
  • [3] Brachmann CB, 1998, YEAST, V14, P115
  • [4] Maintenance of cell integrity in the gas1 mutant of Saccharomyces cerevisiae requires the Chs3p-targeting and activation pathway and involves an unusual Chs3p localization
    Carotti, C
    Ferrario, L
    Roncero, C
    Valdivieso, MH
    Duran, A
    Popolo, L
    [J]. YEAST, 2002, 19 (13) : 1113 - 1124
  • [5] Deresinski SC, 2003, CLIN INFECT DIS, V36, P1445, DOI 10.1086/375080
  • [6] Parallel phenotypic analysis of sporulation and postgermination growth in Saccharomyces cerevisiae
    Deutschbauer, AM
    Williams, RM
    Chu, AM
    Davis, RW
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (24) : 15530 - 15535
  • [7] Mutations in Fks1p affect the cell wall content of β-1,3-and β-1,6-glucan in Saccharomyces cerevisiae
    Dijkgraaf, GJP
    Abe, M
    Ohya, Y
    Bussey, H
    [J]. YEAST, 2002, 19 (08) : 671 - 690
  • [8] DOUGLAS DJA, 1994, COMMUNITY EC DEV CAN, V1, P1
  • [9] Rho1p, a yeast protein at the interface between cell polarization and morphogenesis
    Drgonova, J
    Drgon, T
    Tanaka, K
    Kollar, R
    Chen, GC
    Ford, RA
    Chan, CSM
    Takai, Y
    Cabib, E
    [J]. SCIENCE, 1996, 272 (5259) : 277 - 279
  • [10] Calcofluor antifungal action depends on chitin and a functional high-osmolarity glycerol response (HOG) pathway:: Evidence for a physiological role of the Saccharomyces cerevisiae HOG pathway under noninducing conditions
    García-Rodriguez, LJ
    Durán, A
    Roncero, C
    [J]. JOURNAL OF BACTERIOLOGY, 2000, 182 (09) : 2428 - 2437