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Medicinal genetics approach towards identifying the molecular target of a novel inhibitor of fungal cell wall assembly.
Tsukahara, Kappei; Hata, Katsura; Nakamoto, Kazutaka; Sagane, Koji; Watanabe, Nao-Aki; Kuromitsu, Junro; Kai, Junko; Tsuchiya, Mamiko; Ohba, Fuminori; Jigami, Yoshifumi; Yoshimatsu, Kentaro; Nagasu, Takeshi.
Afiliación
  • Tsukahara K; Tsukuba Research Laboratories, Eisai Co, Ltd, Tsukuba 300-2635, Ibaraki, Japan. k-tsukahara@hhc.eisai.co.jp
Mol Microbiol ; 48(4): 1029-42, 2003 May.
Article en En | MEDLINE | ID: mdl-12753194
ABSTRACT
Glycosylphosphatidylinositol (GPI)-anchored cell wall mannoproteins are required for the adhesion of pathogenic fungi, such as Candida albicans, to human epithelium. Small molecular inhibitors of the cell surface presentation of GPI-anchored mannoproteins would be promising candidate drugs to block the establishment of fungal infections. Here, we describe a medicinal genetics approach to identifying the gene encoding a novel target protein that is required for the localization of GPI-anchored cell wall mannoproteins. By means of a yeast cell-based screening procedure, we discovered a compound, 1-[4-butylbenzyl]isoquinoline (BIQ), that inhibits cell wall localization of GPI-anchored mannoproteins in Saccharomyces cerevisiae. Treatment of C. albicans cells with this compound resulted in reduced adherence to a rat intestine epithelial cell monolayer. A previously uncharacterized gene YJL091c, named GWT1, was cloned as a dosage-dependent suppressor of the BIQ-induced phenotypes. GWT1 knock-out cells showed similar phenotypes to BIQ-treated wild-type cells in terms of cell wall structure and transcriptional profiles. Two different mutants resistant to BIQ each contained a single missense mutation in the coding region of the GWT1 gene. These results all suggest that the GWT1 gene product is the primary target of the compound.
Asunto(s)
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Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Candida albicans / Pared Celular / Glicosilfosfatidilinositoles / Proteínas de Saccharomyces cerevisiae / Isoquinolinas Idioma: En Revista: Mol Microbiol Asunto de la revista: BIOLOGIA MOLECULAR / MICROBIOLOGIA Año: 2003 Tipo del documento: Article País de afiliación: Japón
Buscar en Google
Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Candida albicans / Pared Celular / Glicosilfosfatidilinositoles / Proteínas de Saccharomyces cerevisiae / Isoquinolinas Idioma: En Revista: Mol Microbiol Asunto de la revista: BIOLOGIA MOLECULAR / MICROBIOLOGIA Año: 2003 Tipo del documento: Article País de afiliación: Japón
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