Department of Advanced Bioscience, Graduate School of Agriculture, Kindai University, Nakamachi, Nara, 631-8505, Japan.
Division of Genomics and Breeding, Iwate Biotechnology Research Center, Iwate, 024-0003, Japan.
New Phytol. 2022 Nov;236(4):1441-1454. doi: 10.1111/nph.18439. Epub 2022 Sep 12.
Plant nucleotide-binding leucine-rich repeat receptors (NLRs) initiate immune responses by recognizing pathogen effectors. The rice gene Xa1 encodes an NLR with an N-terminal BED domain, and recognizes transcription activator-like (TAL) effectors of Xanthomonas oryzae pv oryzae (Xoo). Our goal here was to elucidate the molecular mechanisms controlling the induction of immunity by Xa1. We used yeast two-hybrid assays to screen for host factors that interact with Xa1 and identified the AP2/ERF-type transcription factor OsERF101/OsRAP2.6. Molecular complementation assays were used to confirm the interactions among Xa1, OsERF101 and two TAL effectors. We created OsERF101-overexpressing and knockout mutant lines in rice and identified genes differentially regulated in these lines, many of which are predicted to be involved in the regulation of response to stimulus. Xa1 interacts in the nucleus with the TAL effectors and OsERF101 via the BED domain. Unexpectedly, both the overexpression and the knockout lines of OsERF101 displayed Xa1-dependent, enhanced resistance to an incompatible Xoo strain. Different sets of genes were up- or downregulated in the overexpression and knockout lines. Our results indicate that OsERF101 regulates the recognition of TAL effectors by Xa1, and functions as a positive regulator of Xa1-mediated immunity. Furthermore, an additional Xa1-mediated immune pathway is negatively regulated by OsERF101.
植物核苷酸结合富含亮氨酸重复受体(NLRs)通过识别病原体效应子启动免疫反应。水稻基因 Xa1 编码一个具有 N 端 BED 结构域的 NLR,它识别稻黄单胞菌 pv 稻(Xoo)的转录激活子样(TAL)效应子。我们的目标是阐明控制 Xa1 诱导免疫的分子机制。我们使用酵母双杂交试验筛选与 Xa1 相互作用的宿主因子,并鉴定出 AP2/ERF 型转录因子 OsERF101/OsRAP2.6。分子互补试验用于确认 Xa1、OsERF101 和两个 TAL 效应子之间的相互作用。我们在水稻中创建了 OsERF101 过表达和敲除突变体系,并鉴定了这些系中差异调节的基因,其中许多基因预测参与对刺激的反应的调节。Xa1 通过 BED 结构域与 TAL 效应子和 OsERF101 在核内相互作用。出乎意料的是,OsERF101 的过表达和敲除系都表现出对不相容 Xoo 菌株的 Xa1 依赖性增强抗性。过表达和敲除系中上调或下调了不同的基因集。我们的结果表明,OsERF101 调节 Xa1 对 TAL 效应子的识别,并作为 Xa1 介导的免疫的正调节剂起作用。此外,OsERF101 负调节另一个 Xa1 介导的免疫途径。