School of Bio Sciences and Technology, Vellore Institute of Technology, Vellore, 632014, Tamil Nadu, India.
School of Bio Sciences and Technology, Vellore Institute of Technology, Vellore, 632014, Tamil Nadu, India.
Plant Sci. 2019 Mar;280:269-282. doi: 10.1016/j.plantsci.2018.12.017. Epub 2018 Dec 21.
OsWRKY13 TF gene is known to play a regulatory role of signaling in physiological pathways related to either development or disease resistance in rice plants. Rice cultivars IR 50 and TRY 3, resistant and susceptible respectively to sheath blight, TRY 3 and CO 43 resistant and susceptible respectively to sheath rot were challenged with fungal pathogens and disease scoring was carried out. Percent Disease Index (PDI) was significantly higher in susceptible varieties than resistant varieties. RT-PCR and qPCR analyses of WRKY13 using RNA extracted from the plant tissues revealed higher WRKY13 expression in resistant varieties (both diseases) upon pathogen challenge compared to uninfected control and also the susceptible varieties. To compute and evaluate the possible molecular mechanism for observed resistance correlated to WRKY13 gene expression, rice gene expression profiles against bacterial leaf blight and leaf blast disease from ROAD database were used to prioritize the locus IDs that were used as input in RiceNet v2 tool. The expression of WRKY13-regulated TIFY9 gene was predicted and validated using RT-PCR and qRT-PCR along with WRKY12 and PR2. All three genes showed induced expression in R. solani challenged sheath blight resistant variety. WRKY12 and PR2 expression in S. oryzae challenged sheath rot resistant variety was higher. Agrobacterium mediated transformation was carried out in rice plants using overexpression construct of WRKY13 (agroinfection in seeds of varieties susceptible to sheath blight and sheath rot, followed by selection in antibiotic media, germinating and hardening of putative transgenic lines). Based on qPCR analysis, the expression level of WRKY13 and the co-expression levels of WRKY12, TIFY9 and PR2 were found higher in PCR-positive T plants compared to wild-type. Infection bioassays in the transgenic plants of both varieties revealed enhanced resistance to the pathogens. A mechanism by which WRKY13 would influence the MAPK cascade with TIFY9 acting as a mediator, is proposed.
OsWRKY13 TF 基因已知在与水稻植物发育或抗病性相关的生理途径中发挥信号调节作用。对分别对叶鞘枯病具有抗性和敏感性的水稻品种 IR 50 和 TRY 3、对叶鞘腐烂病具有抗性和敏感性的 TRY 3 和 CO 43 进行了真菌病原体挑战,并进行了疾病评分。在易感品种中,病害指数(PDI)显著高于抗性品种。使用从植物组织中提取的 RNA 对 WRKY13 进行 RT-PCR 和 qPCR 分析表明,与未感染对照相比,抗性品种(两种疾病)在受到病原体挑战后 WRKY13 的表达更高,也高于易感品种。为了计算和评估与 WRKY13 基因表达相关的观察到的抗性的可能分子机制,从 ROAD 数据库中使用了针对细菌性条斑病和叶斑病的水稻基因表达谱,以优先考虑作为 RiceNet v2 工具输入的基因座 ID。使用 RT-PCR 和 qRT-PCR 以及 WRKY12 和 PR2 预测和验证了 WRKY13 调节的 TIFY9 基因的表达。在 R. solani 挑战的叶鞘枯病抗性品种中,所有三个基因均显示出诱导表达。在 S. oryzae 挑战的叶鞘腐烂病抗性品种中,WRKY12 和 PR2 的表达更高。使用 WRKY13 的过表达构建体(在对叶鞘枯病和叶鞘腐烂病敏感的品种的种子中进行根癌农杆菌感染,然后在抗生素培养基中进行选择,萌发和硬化潜在的转基因系)对水稻植物进行了农杆菌介导的转化。基于 qPCR 分析,在 PCR 阳性 T 植物中,WRKY13 的表达水平以及 WRKY12、TIFY9 和 PR2 的共表达水平均高于野生型。在两种品种的转基因植物中的感染生物测定表明,对病原体的抗性增强。提出了 WRKY13 通过 TIFY9 作为介质影响 MAPK 级联的机制。