Department of Molecular and Applied Microbiology, Leibniz Institute for Natural Product Research and Infection Biology (HKI), Beutenbergstrasse 11a, D-07745 Jena, Germany.
Mol Microbiol. 2011 Oct;82(1):39-53. doi: 10.1111/j.1365-2958.2011.07778.x. Epub 2011 Aug 30.
The saprophytic fungus Aspergillus fumigatus is the most important air-borne fungal pathogen. The cell wall of A. fumigatus has been studied intensively as a potential target for development of effective antifungal agents. A major role in maintaining cell wall integrity is played by the mitogen-activated protein kinase (MAPK) MpkA. To gain a comprehensive insight into this central signal transduction pathway, we performed a transcriptome analysis of the ΔmpkA mutant under standard and cell wall stress conditions. Besides genes involved in cell wall remodelling, protection against ROS and secondary metabolism such as gliotoxin, pyomelanin and pseurotin A, also genes involved in siderophore biosynthesis were regulated by MpkA. Consistently, northern and western blot analyses indicated that iron starvation triggers phosphorylation and thus activation of MpkA. Furthermore, localization studies indicated that MpkA accumulates in the nucleus under iron depletion. Hence, we report the first connection between a MAPK pathway and siderophore biosynthesis. The measurement of amino acid pools and of the pools of polyamines indicated that arginine was continuously converted into ornithine to fuel the siderophore pool in the ΔmpkA mutant strain. Based on our data, we propose that MpkA fine-tunes the balance between stress response and energy consuming cellular processes.
腐生真菌烟曲霉是最重要的空气传播真菌病原体。烟曲霉的细胞壁作为开发有效抗真菌药物的潜在靶点受到了深入研究。丝裂原活化蛋白激酶 (MAPK) MpkA 在维持细胞壁完整性方面起着重要作用。为了全面了解这一核心信号转导途径,我们在标准和细胞壁应激条件下对 ΔmpkA 突变体进行了转录组分析。除了参与细胞壁重塑、ROS 防御和次生代谢(如Gliotoxin、Pyomelanin 和 Pseurotin A)的基因外,参与铁载体生物合成的基因也受到 MpkA 的调控。一致地, northern 和 western blot 分析表明,缺铁会触发 MpkA 的磷酸化和激活。此外,定位研究表明,MpkA 在缺铁时积累在核内。因此,我们报告了第一个 MAPK 途径与铁载体生物合成之间的联系。氨基酸池和多胺池的测量表明,在 ΔmpkA 突变菌株中,精氨酸不断转化为鸟氨酸,为铁载体池提供燃料。基于我们的数据,我们提出 MpkA 微调了应激反应和能量消耗细胞过程之间的平衡。