Birkenbihl Rainer P, Kracher Barbara, Roccaro Mario, Somssich Imre E
Department of Plant Microbe Interactions, Max Planck Institute for Plant Breeding Research, 50829 Koeln, Germany.
Department of Plant Microbe Interactions, Max Planck Institute for Plant Breeding Research, 50829 Koeln, Germany
Plant Cell. 2017 Jan;29(1):20-38. doi: 10.1105/tpc.16.00681. Epub 2016 Dec 23.
During microbial-associated molecular pattern-triggered immunity (MTI), molecules derived from microbes are perceived by cell surface receptors and upon signaling to the nucleus initiate a massive transcriptional reprogramming critical to mount an appropriate host defense response. WRKY transcription factors play an important role in regulating these transcriptional processes. Here, we determined on a genome-wide scale the flg22-induced in vivo DNA binding dynamics of three of the most prominent WRKY factors, WRKY18, WRKY40, and WRKY33. The three WRKY factors each bound to more than 1000 gene loci predominantly at W-box elements, the known WRKY binding motif. Binding occurred mainly in the 500-bp promoter regions of these genes. Many of the targeted genes are involved in signal perception and transduction not only during MTI but also upon damage-associated molecular pattern-triggered immunity, providing a mechanistic link between these functionally interconnected basal defense pathways. Among the additional targets were genes involved in the production of indolic secondary metabolites and in modulating distinct plant hormone pathways. Importantly, among the targeted genes were numerous transcription factors, encoding predominantly ethylene response factors, active during early MTI, and WRKY factors, supporting the previously hypothesized existence of a WRKY subregulatory network. Transcriptional analysis revealed that WRKY18 and WRKY40 function redundantly as negative regulators of flg22-induced genes often to prevent exaggerated defense responses.
在微生物相关分子模式触发的免疫反应(MTI)过程中,源自微生物的分子被细胞表面受体识别,在向细胞核发出信号后,引发大规模的转录重编程,这对于启动适当的宿主防御反应至关重要。WRKY转录因子在调节这些转录过程中发挥重要作用。在此,我们在全基因组范围内确定了三种最突出的WRKY因子WRKY18、WRKY40和WRKY33在flg22诱导下的体内DNA结合动态。这三种WRKY因子各自与1000多个基因位点结合,主要结合在已知的WRKY结合基序W-box元件上。结合主要发生在这些基因的500 bp启动子区域。许多靶向基因不仅在MTI期间,而且在损伤相关分子模式触发的免疫反应中参与信号感知和转导,为这些功能相互关联的基础防御途径之间提供了一个机制联系。其他靶标包括参与吲哚类次生代谢物产生和调节不同植物激素途径的基因。重要的是,靶向基因中有许多转录因子,主要编码在早期MTI期间活跃的乙烯反应因子和WRKY因子,支持了先前假设的WRKY亚调控网络的存在。转录分析表明,WRKY18和WRKY40作为flg22诱导基因的负调控因子发挥冗余功能,通常可防止过度的防御反应。