Herbert Corentin, Jacquet Christophe, Borel Charlotte, Esquerre-Tugaye Marie-Therese, Dumas Bernard
UMR 5546 CNRS-Université Paul Sabatier, Pôle de Biotechnologie Végétale, 24 Chemin de Borde Rouge, BP17 Auzeville, 31326 Castanet-Tolosan, France.
J Biol Chem. 2002 Aug 9;277(32):29125-31. doi: 10.1074/jbc.M201489200. Epub 2002 May 31.
Phytopathogenic fungi secrete hydrolytic enzymes that degrade plant cell walls, notably pectinases. The signaling pathway(s) that control pectinase gene expression are currently unknown in filamentous fungi. Recently, the green fluorescent protein coding sequence was used as a reporter gene to study the expression of CLPG2, a gene encoding an endopolygalacturonase of the bean pathogen Colletotrichum lindemuthianum. CLPG2 is transcriptionally induced by pectin in the axenic culture of the fungus and during formation of the appressorium, an infection structure specialized in plant tissue penetration. In the present study, promoter deletion and mutagenesis, as well as gel shift mobility assays, allowed for the first time identification of cis-acting elements that bind protein factors and are essential for the regulation of a pectinase gene. We found that two different adjacent DNA motifs are combined to form an active element that shows a strong sequence homology with the yeast filamentation and invasion response element. The same element is required for the transcriptional activation of CLPG2 by pectin and during appressorium development. This study strongly suggests that the control of virulence genes of fungal plant pathogens, such as pectinases, involves the formation of a complex of transcriptional activators similar to those regulating the invasive growth in yeast.
植物病原真菌分泌降解植物细胞壁的水解酶,尤其是果胶酶。目前在丝状真菌中,控制果胶酶基因表达的信号通路尚不清楚。最近,绿色荧光蛋白编码序列被用作报告基因,以研究CLPG2的表达,CLPG2是编码豆类病原菌菜豆炭疽菌一种内切多聚半乳糖醛酸酶的基因。在真菌的无菌培养中以及在附着胞(一种专门用于穿透植物组织的侵染结构)形成过程中,果胶可转录诱导CLPG2。在本研究中,启动子缺失和诱变以及凝胶迁移率变动分析首次鉴定出与蛋白质因子结合且对果胶酶基因调控至关重要的顺式作用元件。我们发现两个不同的相邻DNA基序组合形成一个活性元件,该元件与酵母丝状化和侵袭反应元件具有很强的序列同源性。果胶和附着胞发育过程中CLPG2的转录激活需要相同的元件。这项研究强烈表明,真菌植物病原菌的毒力基因(如果胶酶)的调控涉及转录激活因子复合物的形成,类似于调控酵母侵袭性生长的复合物。