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本文引用的文献

1
Cryptococcus neoformans Ilv2p confers resistance to sulfometuron methyl and is required for survival at 37 degrees C and in vivo.新型隐球菌Ilv2p赋予对甲磺隆的抗性,并且是在37℃和体内存活所必需的。
Microbiology (Reading). 2004 May;150(Pt 5):1547-1558. doi: 10.1099/mic.0.26928-0.
2
Cryptococcus neoformans virulence gene discovery through insertional mutagenesis.通过插入诱变发现新型隐球菌的毒力基因。
Eukaryot Cell. 2004 Apr;3(2):420-9. doi: 10.1128/EC.3.2.420-429.2004.
3
Polarity in filamentous fungi: moving beyond the yeast paradigm.丝状真菌中的极性:超越酵母模式
Fungal Genet Biol. 2004 Apr;41(4):391-400. doi: 10.1016/j.fgb.2003.11.007.
4
Thiol peroxidase is critical for virulence and resistance to nitric oxide and peroxide in the fungal pathogen, Cryptococcus neoformans.硫醇过氧化物酶对于真菌病原体新型隐球菌的毒力以及对一氧化氮和过氧化物的抗性至关重要。
Mol Microbiol. 2004 Mar;51(5):1447-58. doi: 10.1111/j.1365-2958.2004.03921.x.
5
Cryptococcus neoformans gene expression during experimental cryptococcal meningitis.新型隐球菌性脑膜炎实验过程中的新型隐球菌基因表达
Eukaryot Cell. 2003 Dec;2(6):1336-49. doi: 10.1128/EC.2.6.1336-1349.2003.
6
A CLC-type chloride channel gene is required for laccase activity and virulence in Cryptococcus neoformans.新型隐球菌中的漆酶活性和毒力需要一种CLC型氯离子通道基因。
Mol Microbiol. 2003 Nov;50(4):1271-81. doi: 10.1046/j.1365-2958.2003.03752.x.
7
Enzymes that counteract nitrosative stress promote fungal virulence.抵抗亚硝化应激的酶促进真菌致病性。
Curr Biol. 2003 Nov 11;13(22):1963-8. doi: 10.1016/j.cub.2003.10.029.
8
Recapitulation of the sexual cycle of the primary fungal pathogen Cryptococcus neoformans var. gattii: implications for an outbreak on Vancouver Island, Canada.新型隐球菌格特变种主要真菌病原体的性周期概述:对加拿大温哥华岛疫情爆发的影响。
Eukaryot Cell. 2003 Oct;2(5):1036-45. doi: 10.1128/EC.2.5.1036-1045.2003.
9
Phospholipid-binding protein Cts1 controls septation and functions coordinately with calcineurin in Cryptococcus neoformans.磷脂结合蛋白Cts1控制新生隐球菌的隔膜形成,并与钙调神经磷酸酶协同发挥作用。
Eukaryot Cell. 2003 Oct;2(5):1025-35. doi: 10.1128/EC.2.5.1025-1035.2003.
10
Role of alternative oxidase gene in pathogenesis of Cryptococcus neoformans.交替氧化酶基因在新型隐球菌致病机制中的作用。
Infect Immun. 2003 Oct;71(10):5794-802. doi: 10.1128/IAI.71.10.5794-5802.2003.

利用基因组DNA微阵列鉴定新型隐球菌温度调节基因。

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

作者信息

Kraus Peter R, Boily Marie-Josée, Giles Steven S, Stajich Jason E, Allen Andria, Cox Gary M, Dietrich Fred S, Perfect John R, Heitman Joseph

机构信息

Department of Molecular Genetics and Microbiology, 322 CARL Building, Box 3546, Research Dr., Duke University Medical Center, Durham, NC 27710, USA.

出版信息

Eukaryot Cell. 2004 Oct;3(5):1249-60. doi: 10.1128/EC.3.5.1249-1260.2004.

DOI:10.1128/EC.3.5.1249-1260.2004
PMID:15470254
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC522612/
Abstract

The ability to survive and proliferate at 37 degrees C 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 degrees C. Genes with orthologs involved in stress responses were induced during growth at 37 degrees C, 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 degrees C 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 degrees C, 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.

摘要

在37摄氏度下存活和增殖的能力是致病微生物的一种基本毒力属性。利用部分基因组微阵列分析了人类致病真菌新型隐球菌在37摄氏度生长过程中的基因表达情况。在37摄氏度生长过程中,与应激反应相关的直系同源基因被诱导表达,这表明新型隐球菌在应激条件下利用一种保守的转录程序来改变基因表达。一个编码转录因子同源物Mga2的基因在37摄氏度时被诱导表达,并且发现其对高温生长很重要。编码脂肪酸生物合成酶的基因被确定为Mga2的潜在靶点,这表明膜重塑是适应高生长温度的一个重要组成部分。mga2Δ突变体对麦角固醇合成抑制剂氟康唑极其敏感,这表明膜成分前体的合成存在协同作用。出乎意料的是,参与氨基酸和嘧啶生物合成的基因在37摄氏度时受到抑制,但发现这些途径的成分是高温生长所必需的。我们的研究结果证明了即使是部分基因组微阵列在描绘有助于微生物致病的调控级联方面的实用性。