Chongqing Key Laboratory of Application and Safety Control of Genetically Modified Crops, Beibei, Chongqing 400716, China; Biotechnology Research Center, Southwest University, Beibei, Chongqing 400716, China.
Chongqing Key Laboratory of Application and Safety Control of Genetically Modified Crops, Beibei, Chongqing 400716, China; Biotechnology Research Center, Southwest University, Beibei, Chongqing 400716, China.
Plant Commun. 2023 Jul 10;4(4):100596. doi: 10.1016/j.xplc.2023.100596. Epub 2023 Mar 30.
In plant immunity, the mutually antagonistic hormones salicylic acid (SA) and jasmonic acid (JA) are implicated in resistance to biotrophic and necrotrophic pathogens, respectively. Promoters that can respond to both SA and JA signals are urgently needed to engineer plants with enhanced resistance to a broad spectrum of pathogens. However, few natural pathogen-inducible promoters are available for this purpose. To address this problem, we have developed a strategy to synthesize dual SA- and JA-responsive promoters by combining SA- and JA-responsive cis elements based on the interaction between their cognate trans-acting factors. The resulting promoters respond rapidly and strongly to both SA and Methyl Jasmonate (MeJA), as well as different types of phytopathogens. When such a synthetic promoter was used to control expression of an antimicrobial peptide, transgenic plants displayed enhanced resistance to a diverse range of biotrophic, necrotrophic, and hemi-biotrophic pathogens. A dual-inducible promoter responsive to the antagonistic signals auxin and cytokinin was generated in a similar manner, confirming that our strategy can be used for the design of other biotically or abiotically inducible systems.
在植物免疫中,相互拮抗的激素水杨酸 (SA) 和茉莉酸 (JA) 分别参与对生物亲和性和坏死性病原体的抗性。迫切需要能够响应 SA 和 JA 信号的启动子,以工程化具有广谱病原体抗性的植物。然而,为此目的可用的天然病原体诱导启动子很少。为了解决这个问题,我们开发了一种通过基于其同源反式作用因子之间的相互作用组合 SA 和 JA 响应顺式元件来合成双 SA 和 JA 响应启动子的策略。所得到的启动子对 SA 和茉莉酸甲酯 (MeJA) 以及不同类型的植物病原体迅速且强烈地做出响应。当这种合成启动子用于控制抗菌肽的表达时,转基因植物表现出对多种生物亲和性、坏死性和半生物亲和性病原体的增强抗性。以类似的方式生成了对拮抗信号生长素和细胞分裂素双诱导的启动子,证实了我们的策略可用于设计其他生物或非生物诱导系统。