Peng Hsuan-Chieh, Mantelin Sophie, Hicks Glenn R, Takken Frank L W, Kaloshian Isgouhi
Department of Nematology (H.-C.P., S.M., I.K.), Graduate Program in Botany and Plant Sciences (H.-C.P., I.K.), Institute for Integrative Genome Biology and Center for Plant Cell Biology (G.R.H., I.K.), University of California, Riverside, California 92521; and Molecular Plant Pathology, Swammerdam Institute for Life Sciences, University of Amsterdam, 1012 WX Amsterdam, The Netherlands (F.L.W.T.).
Department of Nematology (H.-C.P., S.M., I.K.), Graduate Program in Botany and Plant Sciences (H.-C.P., I.K.), Institute for Integrative Genome Biology and Center for Plant Cell Biology (G.R.H., I.K.), University of California, Riverside, California 92521; and Molecular Plant Pathology, Swammerdam Institute for Life Sciences, University of Amsterdam, 1012 WX Amsterdam, The Netherlands (F.L.W.T.)
Plant Physiol. 2016 Jul;171(3):2211-22. doi: 10.1104/pp.16.00295. Epub 2016 May 19.
Somatic embryogenesis receptor kinases (SERKs) are transmembrane receptors involved in plant immunity. Tomato (Solanum lycopersicum) carries three SERK members. One of these, SlSERK1, is required for Mi-1.2-mediated resistance to potato aphids (Macrosiphum euphorbiae). Mi-1.2 encodes a coiled-coil nucleotide-binding leucine-rich repeat protein that in addition to potato aphids confers resistance to two additional phloem-feeding insects and to root-knot nematodes (Meloidogyne spp.). How SlSERK1 participates in Mi-1.2-mediated resistance is unknown, and no Mi-1.2 cognate pest effectors have been identified. Here, we study the mechanistic involvement of SlSERK1 in Mi-1.2-mediated resistance. We show that potato aphid saliva and protein extracts induce the Mi-1.2 defense marker gene SlWRKY72b, indicating that both saliva and extracts contain a Mi-1.2 recognized effector. Resistant tomato cultivar Motelle (Mi-1.2/Mi-1.2) plants overexpressing SlSERK1 were found to display enhanced resistance to potato aphids. Confocal microscopy revealed that Mi-1.2 localizes at three distinct subcellular compartments: the plasma membrane, cytoplasm, and nucleus. Coimmunoprecipitation experiments in these tomato plants and in Nicotiana benthamiana transiently expressing Mi-1.2 and SlSERK1 showed that Mi-1.2 and SlSERK1 colocalize only in a microsomal complex. Interestingly, bimolecular fluorescence complementation analysis showed that the interaction of Mi-1.2 and SlSERK1 at the plasma membrane distinctively changes in the presence of potato aphid saliva, suggesting a model in which a constitutive complex at the plasma membrane participates in defense signaling upon effector binding.
体细胞胚胎发生受体激酶(SERKs)是参与植物免疫的跨膜受体。番茄(Solanum lycopersicum)有三个SERK成员。其中之一,SlSERK1,是Mi-1.2介导的对马铃薯蚜(Macrosiphum euphorbiae)抗性所必需的。Mi-1.2编码一种卷曲螺旋核苷酸结合富含亮氨酸重复序列蛋白,除了对马铃薯蚜有抗性外,还能抵抗另外两种取食韧皮部的昆虫和根结线虫(Meloidogyne spp.)。SlSERK1如何参与Mi-1.2介导的抗性尚不清楚,且尚未鉴定出Mi-1.2同源的害虫效应子。在这里,我们研究了SlSERK1在Mi-1.2介导的抗性中的作用机制。我们发现马铃薯蚜唾液和蛋白提取物可诱导Mi-1.2防御标记基因SlWRKY72b,这表明唾液和提取物中都含有一种能被Mi-1.2识别的效应子。过表达SlSERK1的抗性番茄品种Motelle(Mi-1.2/Mi-1.2)植株对马铃薯蚜表现出增强的抗性。共聚焦显微镜显示Mi-1.2定位于三个不同的亚细胞区室:质膜、细胞质和细胞核。在这些番茄植株以及瞬时表达Mi-1.2和SlSERK1的本氏烟草中进行的免疫共沉淀实验表明,Mi-1.2和SlSERK1仅在微粒体复合物中共定位。有趣的是,双分子荧光互补分析表明,在马铃薯蚜唾液存在的情况下,质膜上Mi-1.2和SlSERK1的相互作用发生了明显变化,这提示了一个模型,即质膜上的组成型复合物在效应子结合后参与防御信号传导。