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MpkA MAP 激酶模块调节烟曲霉细胞壁完整性信号和黑脓素形成。

The MpkA MAP kinase module regulates cell wall integrity signaling and pyomelanin formation in Aspergillus fumigatus.

机构信息

Department of Molecular and Applied Microbiology, Leibniz Institute for Natural Product Research and Infection Biology-Hans Knöll Institute (HKI), Beutenbergstrasse 11a, 07745 Jena, Germany.

出版信息

Fungal Genet Biol. 2009 Dec;46(12):909-18. doi: 10.1016/j.fgb.2009.08.005. Epub 2009 Aug 26.

Abstract

Aspergillus fumigatus is the most important air-borne fungal pathogen, causing severe infections in immunocompromised patients. Mitogen-activated protein kinase (MAPK) signaling pathways are involved in the regulation of various cellular responses to environmental changes in eukaryotes. Genome Blast analysis revealed that the central core of the cell wall integrity signaling pathway in A. fumigatus is composed of three protein kinases designated Bck1, Mkk2 and MpkA. This pathway is of particular interest because it represents a possible target for new antifungal drugs. Deletion of these genes resulted in severe sensitivity of the mutants against cell wall-disturbing compounds and drastic alterations of the fungal morphology. Western blot analysis demonstrated that Bck1 and Mkk2 directly activate MpkA during vegetative growth and under cell wall stress conditions further confirming that Bck1, Mkk2 and MpkA form a MAP kinase module. Interestingly, this MAP kinase module affects the formation of pyomelanin derived from tyrosine degradation.

摘要

烟曲霉是最重要的空气传播真菌病原体,可导致免疫功能低下的患者发生严重感染。有丝分裂原激活蛋白激酶(MAPK)信号通路参与真核生物对环境变化的各种细胞反应的调节。基因组 Blast 分析表明,烟曲霉细胞壁完整性信号通路的核心由三个蛋白激酶组成,分别命名为 Bck1、Mkk2 和 MpkA。该通路特别有趣,因为它代表了新抗真菌药物的潜在靶标。这些基因的缺失导致突变体对细胞壁破坏化合物的严重敏感性和真菌形态的剧烈改变。Western blot 分析表明,Bck1 和 Mkk2 在营养生长和细胞壁应激条件下直接激活 MpkA,进一步证实 Bck1、Mkk2 和 MpkA 形成一个 MAP 激酶模块。有趣的是,这个 MAP 激酶模块影响酪氨酸降解产生的黑素的形成。

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