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利用拟南芥中的正向遗传学揭示介导黄单胞菌效应因子 XopJ4 识别的免疫信号通路。

Using forward genetics in Nicotiana benthamiana to uncover the immune signaling pathway mediating recognition of the Xanthomonas perforans effector XopJ4.

机构信息

Department of Plant and Microbial Biology, University of California, Berkeley, CA, 94720, USA.

Centre for Tropical Crops and Biocommodities, Queensland University of Technology, Brisbane, Qld, 4001, Australia.

出版信息

New Phytol. 2019 Jan;221(2):1001-1009. doi: 10.1111/nph.15411. Epub 2018 Aug 29.

DOI:10.1111/nph.15411
PMID:30156705
Abstract

The immune pathway responsible for perception of the Xanthomonas perforans effector XopJ4 was identified in the plant Nicotiana benthamiana. This pathogen causes significant yield loss in commercial tomato cultivation. Genetic mapping and viral-induced gene silencing were used to identify immune signaling components of the XopJ4 perception pathway in N. benthamiana. Transient complementation assays were performed to determine the functionality of gene variants and co-immunoprecipitation assays were used to gain insight into the molecular mechanism of the pathway. Two N. benthamiana ethyl methanesulfonate (EMS) mutants deficient for XopJ4 perception were identified as having loss-of-function mutations in the gene encoding the nucleotide binding, leucine-rich repeat (NLR) protein NbZAR1. Silencing of a receptor-like cytoplasmic kinase family XII gene, subsequently named XOPJ4 IMMUNITY 2 (JIM2), blocks perception of XopJ4. This study demonstrates the feasibility of conducting mutant screens in N. benthamiana to investigate the genetic basis of the plant immune system and other processes. The identification of NbZAR1 and JIM2 as mediating XopJ4 perception in N. benthamiana supports the model of ZAR1 being involved in the perception of many different pathogen effector proteins with specificity dictated by associated receptor-like cytoplasmic kinases.

摘要

在植物本氏烟中鉴定出负责感知黄单胞菌效应因子 XopJ4 的免疫途径。这种病原体导致商业番茄种植中产量显著下降。遗传图谱和病毒诱导的基因沉默被用于鉴定本氏烟中 XopJ4 感知途径的免疫信号成分。进行瞬时互补测定以确定基因变异体的功能,并且共免疫沉淀测定用于深入了解该途径的分子机制。鉴定出两个本氏烟乙基甲磺酸(EMS)突变体缺乏 XopJ4 感知功能,其基因编码核苷酸结合,富含亮氨酸重复(NLR)蛋白 NbZAR1 具有功能丧失突变。随后命名为 XOPJ4 IMMUNITY 2(JIM2)的受体样细胞质激酶家族 XII 基因的沉默会阻止 XopJ4 的感知。这项研究证明了在本氏烟中进行突变筛选以研究植物免疫系统和其他过程的遗传基础的可行性。NbZAR1 和 JIM2 被鉴定为在本氏烟中介导 XopJ4 感知,支持 ZAR1 参与许多不同的病原体效应蛋白的感知的模型,特异性由相关的受体样细胞质激酶决定。

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