State Key Laboratory of Hybrid Rice, College of Life Sciences, Wuhan University, Wuhan 430072, China.
State Key Laboratory of Hybrid Rice, College of Life Sciences, Wuhan University, Wuhan 430072, China
Plant Cell. 2017 Dec;29(12):3157-3185. doi: 10.1105/tpc.17.00263. Epub 2017 Nov 1.
(), the first planthopper resistance gene isolated via map-based cloning in rice (), 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 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 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.
BPH14,第一个通过图位克隆在水稻中分离的褐飞虱抗性基因(),编码一个卷曲螺旋、核苷酸结合位点、富含亮氨酸重复(CC-NB-LRR)蛋白。最近已经鉴定出几个编码具有相似结构蛋白的褐飞虱和蚜虫抗性基因。在这里,我们分析了 BPH14 结构域的功能,以确定 BPH14 介导的褐飞虱抗性的分子机制。单独的 CC 或 NB 结构域或它们的组合(CC-NB [CN])赋予与全长(FL)BPH14 相似水平的褐飞虱抗性。这两个结构域都激活了水杨酸信号通路和防御基因表达。在水稻原生质体和叶片中,这些结构域增加了活性氧水平,而不会引发细胞死亡。此外,抗性结构域和 FL BPH14 蛋白形成同源复合物,与转录因子 WRKY46 和 WRKY72 相互作用。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 依赖的转录激活活性。WRKY46 和 WRKY72 结合到受体样细胞质激酶基因和几丁质合成酶基因 LOC_Os01g67364.1 的启动子上,其转录激活活性依赖于 WRKY46 或 WRKY72。这些发现揭示了这一重要的昆虫抗性机制。