Segonzac Cécile, Newman Toby E, Choi Sera, Jayaraman Jay, Choi Du Seok, Jung Ga Young, Cho Heejung, Lee Young Kee, Sohn Kee Hoon
Department of Life Sciences, Pohang University of Science and TechnologyPohang, South Korea.
Plant Science Department, Plant Genomics and Breeding Institute and Research Institute of Agriculture and Life Sciences, College of Agriculture and Life Sciences, Seoul National UniversitySeoul, South Korea.
Front Plant Sci. 2017 Aug 2;8:1330. doi: 10.3389/fpls.2017.01330. eCollection 2017.
is the causal agent of the devastating bacterial wilt disease in many high value crops. secretes around 70 effectors into host cells in order to promote infection. Plants have, however, evolved specialized immune receptors that recognize corresponding effectors and confer qualitative disease resistance. In the model species , the paired immune receptors RRS1 (resistance to 1) and RPS4 (resistance to 4) cooperatively recognize the effector PopP2 in the nuclei of infected cells. PopP2 is an acetyltransferase that binds to and acetylates the RRS1 WRKY DNA-binding domain resulting in reduced RRS1-DNA association thereby activating plant immunity. Here, we surveyed the naturally occurring variation in PopP2 sequence among the strains isolated from diseased tomato and pepper fields across the Republic of Korea. Our analysis revealed high conservation of sequence with only three polymorphic alleles present amongst 17 strains. Only one variation (a premature stop codon) caused the loss of RPS4/RRS1-dependent recognition in Arabidopsis. We also found that PopP2 harbors a putative eukaryotic transcriptional repressor motif (ethylene-responsive element binding factor-associated amphiphilic repression or EAR), which is known to be involved in the recruitment of transcriptional co-repressors. Remarkably, mutation of the EAR motif disabled PopP2 avirulence function as measured by the development of hypersensitive response, electrolyte leakage, defense marker gene expression and bacterial growth in Arabidopsis. This lack of recognition was partially but significantly reverted by the C-terminal addition of a synthetic EAR motif. We show that the EAR motif-dependent gain of avirulence correlated with the stability of the PopP2 protein. Furthermore, we demonstrated the requirement of the PopP2 EAR motif for PTI suppression. A yeast two-hybrid screen indicated that PopP2 does not interact with any well-known Arabidopsis transcriptional co-repressors. Overall, this study reveals high conservation of the PopP2 effector in Korean strains isolated from commercially cultivated tomato and pepper genotypes. Importantly, our data also indicate that the PopP2 conserved repressor motif could contribute to the effector accumulation in plant cells.
是许多高价值作物中毁灭性青枯病的致病因子。它向宿主细胞分泌约70种效应蛋白以促进感染。然而,植物已经进化出专门的免疫受体,这些受体识别相应的效应蛋白并赋予定性抗病性。在模式植物物种中,配对的免疫受体RRS1(对1号菌的抗性)和RPS4(对4号菌的抗性)在受感染细胞的细胞核中协同识别效应蛋白PopP2。PopP2是一种乙酰转移酶,它与RRS1的WRKY DNA结合结构域结合并使其乙酰化,导致RRS1与DNA的结合减少,从而激活植物免疫。在这里,我们调查了从韩国各地患病番茄和辣椒田分离的菌株中PopP2序列的自然变异。我们的分析揭示了该序列的高度保守性,在17个菌株中仅存在三个多态性等位基因。只有一个变异(一个提前终止密码子)导致拟南芥中RPS4/RRS1依赖性识别的丧失。我们还发现PopP2含有一个假定的真核转录抑制基序(乙烯反应元件结合因子相关两亲性抑制或EAR),已知该基序参与转录共抑制因子的募集。值得注意的是,通过过敏反应的发展、电解质渗漏、防御标记基因表达和拟南芥中的细菌生长来衡量,EAR基序的突变使PopP2的无毒功能丧失。通过在C末端添加合成EAR基序,这种识别缺失部分但显著地得到了恢复。我们表明,依赖EAR基序的无毒获得与PopP2蛋白的稳定性相关。此外,我们证明了PopP2 EAR基序对PTI抑制的必要性。酵母双杂交筛选表明PopP2不与任何已知的拟南芥转录共抑制因子相互作用。总体而言,这项研究揭示了从商业种植的番茄和辣椒基因型中分离的韩国菌株中PopP2效应蛋白的高度保守性。重要的是,我们的数据还表明,PopP2保守的抑制基序可能有助于效应蛋白在植物细胞中的积累。