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The Coiled-Coil and Nucleotide Binding Domains of BROWN PLANTHOPPER RESISTANCE14 Function in Signaling and Resistance against Planthopper in Rice

机译:水稻褐飞虱抗性14的螺旋线圈和核苷酸结合域在水稻信号传导和抗稻飞虱中的作用

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摘要

BROWN PLANTHOPPER RESISTANCE14 (BPH14), the first planthopper resistance gene isolated via map-based cloning in rice (Oryza sativa), encodes a coiled-coil, nucleotide binding site, leucine-rich repeat (CC-NB-LRR) protein. Several planthopper and aphid resistance genes encoding proteins with similar structures have recently been identified. Here, we analyzed the functions of the domains of BPH14 to identify molecular mechanisms underpinning BPH14-mediated planthopper resistance. The CC or NB domains alone or in combination (CC-NB [CN]) conferred a similar level of brown planthopper resistance to that of full-length (FL) BPH14. Both domains activated the salicylic acid signaling pathway and defense gene expression. In rice protoplasts and Nicotiana benthamiana leaves, these domains increased reactive oxygen species levels without triggering cell death. Additionally, the resistance domains and FL BPH14 protein formed homocomplexes that interacted with transcription factors WRKY46 and WRKY72. In rice protoplasts, the expression of FL BPH14 or its CC, NB, and CN domains increased the accumulation of WRKY46 and WRKY72 as well as WRKY46- and WRKY72-dependent transactivation activity. WRKY46 and WRKY72 bind to the promoters of the receptor-like cytoplasmic kinase gene RLCK281 and the callose synthase gene LOC_Os01g67364.1, whose transactivation activity is dependent on WRKY46 or WRKY72. These findings shed light on this important insect resistance mechanism.
机译:通过在水稻(Oryza sativa)中基于图谱的克隆分离出的第一个飞虱抗性基因BROWN PLANTHOPPER RESISTANCE14(BPH14)编码卷曲螺旋,核苷酸结合位点,富含亮氨酸的重复序列(CC-NB-LRR)蛋白。最近已经鉴定了几种编码具有相似结构的蛋白质的飞虱和蚜虫抗性基因。在这里,我们分析了BPH14域的功能,以识别支撑BPH14介导的飞虱抗性的分子机制。单独或组合的CC或NB结构域(CC-NB [CN])赋予的褐飞虱抗性水平与全长(FL)BPH14相似。两个结构域均激活水杨酸信号传导途径和防御基因表达。在水稻原生质体和本生烟草叶片中,这些域在不触发细胞死亡的情况下增加了活性氧水平。另外,抗性结构域和FL BPH14蛋白形成与转录因子WRKY46和WRKY72相互作用的同质复合体。在水稻原生质体中,FL BPH14或其CC,NB和CN结构域的表达增加了WRKY46和WRKY72的积累以及WRKY46和WRKY72依赖性反式激活活性。 WRKY46和WRKY72与受体样细胞质激酶基因RLCK281和the质合酶基因LOC_Os01g67364.1的启动子结合,后者的反式激活活性取决于WRKY46或WRKY72。这些发现阐明了这种重要的抗虫机制。

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