Walton Felicia J, Idnurm Alexander, Heitman Joseph
Howard Hughes Medical Institute, Department of Molecular Genetics and Microbiology, Duke University Medical Center, Durham, NC 27710, USA.
Mol Microbiol. 2005 Sep;57(5):1381-96. doi: 10.1111/j.1365-2958.2005.04779.x.
The ability to produce melanin is a key virulence factor in many fungal pathogens including the human basidiomycete pathogen Cryptococcus neoformans, a major cause of life-threatening infections among immunocompromised persons. Despite the significance of melanin biosynthesis in virulence of C. neoformans, the cellular and molecular processes involved in this pathway have not yet been fully elucidated. Here, we used Agrobacterium to isolate insertional mutants and screened 12 000 mutants to uncover genes involved in melanin production in C. neoformans. Four new mutant alleles of the well-known melanin biosynthesis gene, LAC1, which encodes laccase were identified, and the T-DNA was shown to have a possible predisposition for insertion into the promoters of genes, in particular LAC1. Melanization in C. neoformans is dependent on five additional genes identified in this screen encoding homologues of the copper transporter Ccc2, the copper chaperone Atx1, the chitin synthase Chs3, the transcriptional coactivator Mbf1 and the chromatin-remodelling enzyme Snf5. Illumination of the molecular and genetic components of this virulence pathway reveals potential novel targets for drug development against C. neoformans and provides further insight into the intimate relationship between metal ion homeostasis and melanin biosynthesis.
产生黑色素的能力是许多真菌病原体的关键毒力因子,包括人类担子菌病原体新型隐球菌,它是免疫功能低下人群中危及生命的感染的主要原因。尽管黑色素生物合成在新型隐球菌的毒力中具有重要意义,但该途径所涉及的细胞和分子过程尚未完全阐明。在这里,我们利用农杆菌分离插入突变体,并筛选了12000个突变体,以发现新型隐球菌中参与黑色素产生的基因。我们鉴定出了著名的黑色素生物合成基因LAC1(编码漆酶)的四个新突变等位基因,并且显示T-DNA可能倾向于插入基因的启动子中,特别是LAC1的启动子。新型隐球菌中的黑色素化取决于在此筛选中鉴定出的另外五个基因,它们编码铜转运蛋白Ccc2、铜伴侣蛋白Atx1、几丁质合酶Chs3、转录共激活因子Mbf1和染色质重塑酶Snf5的同源物。阐明这条毒力途径的分子和遗传成分,揭示了针对新型隐球菌进行药物开发的潜在新靶点,并进一步深入了解了金属离子稳态与黑色素生物合成之间的密切关系。