Plant Genomics Laboratory, Genome Research Center, KRIBB, PO Box 115, Yusung, Taejon, 305-600, Republic of Korea.
Mol Plant Pathol. 2005 May 1;6(3):269-85. doi: 10.1111/j.1364-3703.2005.00284.x.
SUMMARY To understand better the defence responses of plants to pathogen attack, we challenged hot pepper plants with bacterial pathogens and identified transcription factor-encoding genes whose expression patterns were altered during the subsequent hypersensitive response. One of these genes, CaPIF1 (Capsicum annuum Pathogen-Induced Factor 1), was characterized further. This gene encodes a plant-specific EPF-type protein that contains two Cys(2)/His(2) zinc fingers. CaPIF1 expression was rapidly and specifically induced when pepper plants were challenged with bacterial pathogens to which they are resistant. In contrast, challenge with a pathogen to which the plants are susceptible only generated weak CaPIF1 expression. CaPIF1 expression was also strongly induced in pepper leaves by the exogenous application of ethephon, an ethylene-releasing compound, and salicylic acid, whereas methyl jasmonate had only moderate effects. CaPIF1 localized to the nuclei of onion epidermis when expressed as a CaPIF1-smGFP fusion protein. Transgenic tobacco plants over-expressing CaPIF1 driven by the CaMV 35S promoter showed increased resistance to challenge with a tobacco-specific pathogen or non-host bacterial pathogens. These plants also showed constitutive up-regulation of multiple defence-related genes. Moreover, virus-induced silencing of the CaPIF1 orthologue in Nicotiana benthamiana enhanced susceptibility to the same host or non-host bacterial pathogens. These observations provide evidence that an EPF-type Cys(2)/His(2) zinc-finger protein plays a crucial role in the activation of the pathogen defence response in plants.
为了更好地理解植物对病原体攻击的防御反应,我们用细菌病原体挑战辣椒植物,并鉴定了在随后的过敏反应中表达模式发生改变的转录因子编码基因。其中一个基因,CaPIF1(辣椒病原体诱导因子 1),进一步进行了特征描述。该基因编码一种植物特异性的 EPF 型蛋白,含有两个 Cys2/His2 锌指。当辣椒植物受到其具有抗性的细菌病原体攻击时,CaPIF1 的表达迅速且特异性地被诱导。相比之下,用植物易感性的病原体进行挑战只会产生较弱的 CaPIF1 表达。外源施用乙烯释放化合物乙膦和水杨酸也强烈诱导 CaPIF1 在辣椒叶片中的表达,而茉莉酸甲酯仅有适度的作用。当作为 CaPIF1-smGFP 融合蛋白表达时,CaPIF1 定位于洋葱表皮细胞的细胞核中。由 CaMV 35S 启动子驱动的过表达 CaPIF1 的转基因烟草植物对烟草特异性病原体或非宿主细菌病原体的挑战表现出更高的抗性。这些植物还表现出多个防御相关基因的组成性上调。此外,在 Nicotiana benthamiana 中病毒诱导沉默 CaPIF1 同源物增强了对相同宿主或非宿主细菌病原体的敏感性。这些观察结果提供了证据,表明 EPF 型 Cys2/His2 锌指蛋白在植物病原体防御反应的激活中起着至关重要的作用。