Liu Hao, Dong Shuangyu, Gu Fengwei, Liu Wei, Yang Guili, Huang Ming, Xiao Wuming, Liu Yongzhu, Guo Tao, Wang Hui, Chen Zhiqiang, Wang Jiafeng
National Engineering Research Center of Plant Space Breeding, South China Agricultural University Guangzhou, China.
Front Plant Sci. 2017 Feb 6;8:127. doi: 10.3389/fpls.2017.00127. eCollection 2017.
The regulation of innate immunity and plant growth, along with the trade-off between them, affects the defense and recovery mechanisms of the plant after it is attacked by pathogens. Although it is known that hormonal crosstalk plays a major role in regulating interaction of plant growth and PAMP-triggered immunity, the relationship between plant growth and effector-triggered immunity (ETI) remains unclear. In a large-scale yeast two-hybrid screening for Pik-H4-interacting proteins, a homeodomain transcription factor OsBIHD1 was identified, which is previously known to function in biotic and abiotic stress responses. The knockout of in rice lines carrying largely compromised the resistance of the rice lines to , the fungus that causes rice blast. While overexpression of resulted in enhanced expression of the pathogenesis-related () and ethylene (ET) synthesis genes. Moreover, OsBIHD1 was also found to directly bind to the promoter region of ethylene-synthesis enzyme OsACO3. In addition, overexpression or deficiency provoked dwarfism and reduced brassinosteroid (BR) insensitivity through repressing the expression of several critical genes involved in BR biosynthesis and BR signaling. During infection, transcript levels of the crucial BR catabolic genes (, , and ) were significantly up-regulated in plants. Furthermore, OsBIHD1 was found to be capable of binding to the sequence-specific -elements on the promoters of to suppress the plant growth under fungal invasion. Our results collectively suggest a model that OsBIHD1 is required for Pik-H4-mediated blast resistance through modulating the trade-off between resistance and growth by coordinating brassinosteroid-ethylene pathway.
植物先天免疫与生长的调控,以及二者之间的权衡,影响着植物在受到病原体攻击后的防御和恢复机制。尽管已知激素间的相互作用在调节植物生长与模式触发免疫(PTI)的相互作用中起主要作用,但植物生长与效应子触发免疫(ETI)之间的关系仍不清楚。在一项针对与Pik-H4相互作用蛋白的大规模酵母双杂交筛选中,鉴定出一个同源域转录因子OsBIHD1,该转录因子先前已知在生物和非生物胁迫响应中发挥作用。在携带Pik-H4的水稻品系中敲除OsBIHD1,极大地损害了水稻品系对稻瘟病菌Magnaporthe oryzae的抗性。而OsBIHD1的过表达导致病程相关(PR)基因和乙烯(ET)合成基因的表达增强。此外,还发现OsBIHD1直接与乙烯合成酶OsACO3的启动子区域结合。另外,OsBIHD1的过表达或缺失通过抑制参与油菜素内酯(BR)生物合成和BR信号传导的几个关键基因的表达,引发矮化并降低对BR的敏感性。在Magnaporthe oryzae感染期间,OsBIHD1敲除植物中关键BR分解代谢基因(OsDWF4、OsBAS1和OsBRI1)的转录水平显著上调。此外,发现OsBIHD1能够结合OsDWF4、OsBAS1和OsBRI1启动子上的序列特异性顺式作用元件,以在真菌入侵下抑制植物生长。我们的研究结果共同提出了一个模型,即OsBIHD1通过协调油菜素内酯-乙烯途径调节抗性与生长之间的权衡,从而在Pik-H4介导的稻瘟病抗性中发挥作用。