Adachi Hiroaki, Nakano Takaaki, Miyagawa Noriko, Ishihama Nobuaki, Yoshioka Miki, Katou Yuri, Yaeno Takashi, Shirasu Ken, Yoshioka Hirofumi
Graduate School of Bioagricultural Sciences, Nagoya University, Nagoya 464-8601, Japan.
ZEN-NOH, Hiratsuka 254-0016, Japan.
Plant Cell. 2015 Sep;27(9):2645-63. doi: 10.1105/tpc.15.00213. Epub 2015 Sep 15.
Pathogen attack sequentially confers pattern-triggered immunity (PTI) and effector-triggered immunity (ETI) after sensing of pathogen patterns and effectors by plant immune receptors, respectively. Reactive oxygen species (ROS) play pivotal roles in PTI and ETI as signaling molecules. Nicotiana benthamiana RBOHB, an NADPH oxidase, is responsible for both the transient PTI ROS burst and the robust ETI ROS burst. Here, we show that RBOHB transactivation mediated by MAPK contributes to R3a/AVR3a-triggered ETI (AVR3a-ETI) ROS burst. RBOHB is markedly induced during the ETI and INF1-triggered PTI (INF1-PTI), but not flg22-tiggered PTI (flg22-PTI). We found that the RBOHB promoter contains a functional W-box in the R3a/AVR3a and INF1 signal-responsive cis-element. Ectopic expression of four phospho-mimicking mutants of WRKY transcription factors, which are MAPK substrates, induced RBOHB, and yeast one-hybrid analysis indicated that these mutants bind to the cis-element. Chromatin immunoprecipitation assays indicated direct binding of the WRKY to the cis-element in plants. Silencing of multiple WRKY genes compromised the upregulation of RBOHB, resulting in impairment of AVR3a-ETI and INF1-PTI ROS bursts, but not the flg22-PTI ROS burst. These results suggest that the MAPK-WRKY pathway is required for AVR3a-ETI and INF1-PTI ROS bursts by activation of RBOHB.
病原体攻击在植物免疫受体分别感知病原体模式和效应子后,依次赋予模式触发免疫(PTI)和效应子触发免疫(ETI)。活性氧(ROS)作为信号分子在PTI和ETI中发挥关键作用。烟草中的NADPH氧化酶RBOHB负责PTI中短暂的ROS爆发以及ETI中强烈的ROS爆发。在此,我们表明由丝裂原活化蛋白激酶(MAPK)介导的RBOHB反式激活有助于R3a/AVR3a触发的ETI(AVR3a-ETI)ROS爆发。RBOHB在ETI和INF1触发的PTI(INF1-PTI)过程中显著诱导,但在flg22触发的PTI(flg22-PTI)过程中不诱导。我们发现RBOHB启动子在R3a/AVR3a和INF1信号响应顺式元件中含有一个功能性W盒。作为MAPK底物的WRKY转录因子的四个磷酸化模拟突变体的异位表达诱导了RBOHB,酵母单杂交分析表明这些突变体与顺式元件结合。染色质免疫沉淀分析表明WRKY在植物中直接与顺式元件结合。多个WRKY基因的沉默损害了RBOHB的上调,导致AVR3a-ETI和INF1-PTI的ROS爆发受损,但不影响flg22-PTI的ROS爆发。这些结果表明,MAPK-WRKY途径通过激活RBOHB对AVR3a-ETI和INF1-PTI的ROS爆发是必需的。