RESUMEN

Converting the complete genome sequence of Candida albicans into meaningful biological information will require comprehensive screens for identifying functional classes of genes. Most systems described so far are not applicable to C. albicans because of its difficulty with mating, its diploid nature, and the lack of functional random insertional mutagenesis methods. We examined artificial gene suppression as a means to identify gene products critical for growth of this pathogen; these represent new antifungal drug targets. To achieve gene suppression we combined antisense RNA inhibition and promoter interference. After cloning antisense complementary DNA (cDNA) fragments under control of an inducible GAL1 promoter, we transferred the resulting libraries to C. albicans. Over 2,000 transformant colonies were screened for a promoter-induced diminished-growth phenotype. After recovery of the plasmids, sequence determination of their inserts revealed the messenger RNA (mRNA) they inhibited or the gene they disrupted. Eighty-six genes critical for growth were identified, 45 with unknown function. When used in high-throughput screening for antifungals, the crippled C. albicans strains generated in this study showed enhanced sensitivity to specific drugs.

Asunto(s)

Candida albicans/crecimiento & desarrollo , Candida albicans/genética , Genes Fúngicos/genética , Genoma Fúngico , Genómica/métodos , ARN sin Sentido/genética , Antifúngicos/farmacología , Candida albicans/efectos de los fármacos , Clonación Molecular/métodos , ADN sin Sentido/genética , Evaluación Preclínica de Medicamentos , Proteínas Fúngicas/genética , Proteínas Fúngicas/metabolismo , Regulación Fúngica de la Expresión Génica , Biblioteca de Genes , Genes Esenciales/genética , Heterocigoto , Pruebas de Sensibilidad Microbiana , Mutagénesis Insercional/genética , Fenotipo , Regiones Promotoras Genéticas/genética , ARN de Hongos/análisis , ARN de Hongos/genética , ARN Mensajero/análisis , ARN Mensajero/genética , Transformación Genética