Ellis Jeffrey G, Dodds Peter N, Lawrence Gregory J
Commonwealth Scientific and Industrial Research Organisation, Division of Plant Industry, GPO Box 1600, Canberra ACT 2601, Australia.
Curr Opin Microbiol. 2007 Aug;10(4):326-31. doi: 10.1016/j.mib.2007.05.015. Epub 2007 Aug 14.
Five unrelated avirulence (Avr) gene families have been cloned from flax rust and barley powdery mildew, fungal pathogens that make close contact with living host plant cells using specialized feeding structures called haustoria. Transgenic expression studies indicate Avr proteins are recognized by disease resistance (R) proteins within host cells, which suggests that Avr proteins are transported via an as yet unidentified route from the fungus to the host during infection. Recognition of flax rust AvrL567 proteins is by direct R-Avr protein interaction. Virulence effector functions have been demonstrated for barley powdery mildew Avr proteins Avra10 and Avrk1. Mildew resistance triggered by Avra10 in barley involves association of the cognate barley R protein Mla10 and transcriptional repressor proteins, including HvWRKY2, in the host nucleus. High amplitude defence gene expression has a dual dependence on transcriptional de-repression induced by specific R-Avr protein recognition and additionally, activation signals initiated by host perception of general pathogen molecules.
已从亚麻锈菌和大麦白粉病中克隆出五个不相关的无毒(Avr)基因家族,这两种真菌病原体利用称为吸器的特殊取食结构与活的寄主植物细胞紧密接触。转基因表达研究表明,Avr蛋白被寄主细胞内的抗病(R)蛋白识别,这表明在感染过程中,Avr蛋白通过一条尚未明确的途径从真菌转运到寄主。亚麻锈菌AvrL567蛋白的识别是通过R-Avr蛋白直接相互作用实现的。已证明大麦白粉病Avr蛋白Avra10和Avrk1具有毒力效应功能。Avra10在大麦中引发的抗白粉病反应涉及寄主细胞核中同源大麦R蛋白Mla10与转录抑制蛋白(包括HvWRKY2)的结合。高幅度防御基因表达双重依赖于由特定R-Avr蛋白识别诱导的转录去抑制,此外还依赖于寄主对一般病原体分子感知引发的激活信号。