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致病疫霉RXLR效应蛋白PexRD2与宿主促分裂原活化蛋白激酶激酶激酶ε相互作用以抑制植物免疫信号传导。

Phytophthora infestans RXLR effector PexRD2 interacts with host MAPKKK ε to suppress plant immune signaling.

作者信息

King Stuart R F, McLellan Hazel, Boevink Petra C, Armstrong Miles R, Bukharova Tatyana, Sukarta Octavina, Win Joe, Kamoun Sophien, Birch Paul R J, Banfield Mark J

机构信息

Department of Biological Chemistry, John Ines Centre, Norwich NR4 7UH, United Kingdom.

出版信息

Plant Cell. 2014 Mar;26(3):1345-59. doi: 10.1105/tpc.113.120055. Epub 2014 Mar 14.

Abstract

Mitogen-activated protein kinase cascades are key players in plant immune signaling pathways, transducing the perception of invading pathogens into effective defense responses. Plant pathogenic oomycetes, such as the Irish potato famine pathogen Phytophthora infestans, deliver RXLR effector proteins to plant cells to modulate host immune signaling and promote colonization. Our understanding of the molecular mechanisms by which these effectors act in plant cells is limited. Here, we report that the P. infestans RXLR effector PexRD2 interacts with the kinase domain of MAPKKKε, a positive regulator of cell death associated with plant immunity. Expression of PexRD2 or silencing MAPKKKε in Nicotiana benthamiana enhances susceptibility to P. infestans. We show that PexRD2 perturbs signaling pathways triggered by or dependent on MAPKKKε. By contrast, homologs of PexRD2 from P. infestans had reduced or no interaction with MAPKKKε and did not promote disease susceptibility. Structure-led mutagenesis identified PexRD2 variants that do not interact with MAPKKKε and fail to support enhanced pathogen growth or perturb MAPKKKε signaling pathways. Our findings provide evidence that P. infestans RXLR effector PexRD2 has evolved to interact with a specific host MAPKKK to perturb plant immunity-related signaling.

摘要

丝裂原活化蛋白激酶级联反应是植物免疫信号通路中的关键参与者,可将对入侵病原体的感知转化为有效的防御反应。植物致病卵菌,如导致爱尔兰马铃薯饥荒的致病疫霉,会将RXLR效应蛋白传递到植物细胞中,以调节宿主免疫信号并促进定殖。我们对这些效应蛋白在植物细胞中发挥作用的分子机制的了解有限。在此,我们报道致病疫霉的RXLR效应蛋白PexRD2与MAPKKKε的激酶结构域相互作用,MAPKKKε是一种与植物免疫相关的细胞死亡正调控因子。在本氏烟草中表达PexRD2或沉默MAPKKKε会增强对致病疫霉的易感性。我们表明,PexRD2会干扰由MAPKKKε触发或依赖于MAPKKKε的信号通路。相比之下,致病疫霉中PexRD2的同源物与MAPKKKε的相互作用减弱或没有相互作用,并且不会促进疾病易感性。基于结构的诱变鉴定出了不与MAPKKKε相互作用、无法支持病原体生长增强或干扰MAPKKKε信号通路的PexRD2变体。我们的研究结果提供了证据,证明致病疫霉的RXLR效应蛋白PexRD2已经进化到可以与特定的宿主MAPKKK相互作用,从而干扰植物免疫相关信号。

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