Identification of Cryptococcus neoformans temperature-regulated genes with a genomic-DNA microarray

被引:75
作者
Kraus, PR
Boily, MJ
Giles, SS
Stajich, JE
Allen, A
Cox, GM
Dietrich, FS
Perfect, JR
Heitman, J
机构
[1] Duke Univ, Ctr Med, Dept Mol Genet & Microbiol, Durham, NC 27710 USA
[2] Duke Univ, Ctr Med, Dept Med, Durham, NC 27710 USA
[3] Duke Univ, Ctr Med, Dept Pharmacol & Canc Biol, Durham, NC 27710 USA
[4] Duke Univ, Ctr Med, Howard Hughes Med Inst, Durham, NC 27710 USA
关键词
D O I
10.1128/EC.3.5.1249-1260.2004
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The ability to survive and proliferate at 37 degreesC is an essential virulence attribute of pathogenic microorganisms. A partial-genome microarray was used to profile gene expression in the human-pathogenic fungus Cryptococcus neoformans during growth at 37 degreesC. Genes with orthologs involved in stress responses were induced during growth at 37 degreesC, suggesting that a conserved transcriptional program is used by C. neoformans to alter gene expression during stressful conditions. A gene encoding the transcription factor homolog Mga2 was induced at 37 degreesC and found to be important for high-temperature growth. Genes encoding fatty acid biosynthetic enzymes were identified as potential targets of Mga2, suggesting that membrane remodeling is an important component of adaptation to high growth temperatures. mga2Delta mutants were extremely sensitive to the ergosterol synthesis inhibitor fluconazole, indicating a coordination of the synthesis of membrane component precursors. Unexpectedly, genes involved in amino acid and pyrimidine biosynthesis were repressed at 37 degreesC, but components of these pathways were found to be required for high-temperature growth. Our findings demonstrate the utility of even partial-genome microarrays for delineating regulatory cascades that contribute to microbial pathogenesis.
引用
收藏
页码:1249 / 1260
页数:12
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