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CLNR1是植物真菌病原体菜豆炭疽菌中类似AREA/NIT2的全局氮调节因子,是感染周期所必需的。

CLNR1, the AREA/NIT2-like global nitrogen regulator of the plant fungal pathogen Colletotrichum lindemuthianum is required for the infection cycle.

作者信息

Pellier Anne-Laure, Laugé Richard, Veneault-Fourrey Claire, Langin Thierry

机构信息

Laboratoire de Phytopathologie Moléculaire, Institut de Biotechnologie des Plantes, Bâtiment 630, Université de Paris-Sud XI, 91405 Orsay Cedex, France.

出版信息

Mol Microbiol. 2003 May;48(3):639-55. doi: 10.1046/j.1365-2958.2003.03451.x.

Abstract

Nitrogen starvation is generally assumed to be encountered by biotrophic and hemibiotrophic plant fungal pathogens at the beginning of their infection cycle. We tested whether nitrogen starvation constitutes a cue regulating genes that are required for pathogenicity of Colletotrichum lindemuthianum, a fungal pathogen of common bean. The clnr1 (C. lindemuthianumnitrogen regulator 1) gene, the areA/nit-2 orthologue of C. lindemuthianum, was isolated. The predicted CLNR1 protein exhibits high amino acid sequence similarities with the AREA and NIT2 global fungal nitrogen regulators. Targeted clnr1- mutants are unable to use a wide array of nitrogen sources, indicating that clnr1 is the C. lindemuthianum major nitrogen regulatory gene. The clnr1- mutants are non-pathogenic, although few anthracnose lesions seldom occur on whole plantlets. Surprisingly, cytological analysis reveals that the clnr1- mutants are not disturbed from the penetration stage until the end of the biotrophic phase, but that they are impaired during the setting up of the necrotrophic phase. Thus, through CLNR1, nitrogen starvation constitutes a cue for the regulation of genes that are compulsory for this stage of the C. lindemuthianum infection process. Additionally, clnr1- mutants complemented with the Aspergillus nidulans areA gene are fully pathogenic, indicating that areA is able to activate the C. lindemuthianum suited genes, normally under the control of clnr1.

摘要

一般认为,活体营养型和半活体营养型植物真菌病原体在其感染周期开始时会遭遇氮饥饿。我们测试了氮饥饿是否构成一种信号,可调节菜豆真菌病原体菜豆炭疽菌致病所需的基因。分离出了菜豆炭疽菌的clnr1(菜豆炭疽菌氮调节因子1)基因,它是构巢曲霉areA/nit-2的直系同源基因。预测的CLNR1蛋白与AREA和NIT2这两种真菌全局氮调节因子具有高度的氨基酸序列相似性。靶向的clnr1突变体无法利用多种氮源,这表明clnr1是菜豆炭疽菌的主要氮调节基因。clnr1突变体无致病性,不过在整个小植株上很少会出现一些炭疽病病斑。令人惊讶的是,细胞学分析表明,clnr1突变体从穿透阶段到活体营养阶段结束都未受干扰,但在坏死营养阶段的建立过程中受到了损害。因此,通过CLNR1,氮饥饿构成了一种信号,用于调节菜豆炭疽菌感染过程这一阶段所必需的基因。此外,用构巢曲霉areA基因互补的clnr1突变体具有完全致病性,这表明areA能够激活通常受clnr1控制的菜豆炭疽菌适宜基因。

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