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Bacillus cereus AR156 triggers induced systemic resistance against Pseudomonas syringae pv. tomato DC3

机译:蜡状芽孢杆菌AR156引发针对丁香假单胞菌PV的诱导的全身抗性。番茄DC3

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摘要

Small RNAs play an important role in plant innate immunity. However, their regulatory function in induced systemic resistance (ISR) triggered by plant growth‐promoting rhizobacteria remains unclear. Here, using as a model system, one plant endogenous small RNA, miR472, was identified as an important regulator involved in the process of AR156 ISR against pv. (Pst) DC3000. The results revealed that miR472 was down‐regulated with AR156 treatment by comparing small RNA profiles and northern blot analysis of with or without AR156 treatment. Plants overexpressing miR472 showed higher susceptibility to Pst DC3000; by contrast, plant lines with miR472 knocked down/out showed the opposite. The transcriptome sequencing revealed thousands of differentially expressed genes in the transgenic plants. Target prediction showed that miR472 targets lots of coiled coil nucleotide‐binding site (NBS) and leucine‐rich repeat (LRR) type resistance genes and the expression of these targets was negatively correlated with the expression of miR472. In addition, transgenic plants with knocked‐out target genes exhibited decreased resistance to Pst DC3000 invasion. Quantitative reverse transcription PCR results indicated that target genes of miR472 were expressed during the process of AR156‐triggered ISR. Taken together, our results demonstrate that the miR472‐mediated silencing pathway is an important regulatory checkpoint occurring via post‐transcriptional control of NBS‐LRR genes during AR156‐triggered ISR in .
机译:小RNA在植物固有免疫中起重要作用。但是,它们在促进植物生长的根际细菌引发的诱导的系统抗性(ISR)中的调节功能尚不清楚。在这里,作为模型系统,一种植物内源小RNA miR472被确定为参与针对pv的AR156 ISR过程的重要调控因子。 (Pst)DC3000。结果表明,通过比较小RNA谱和经过或未经过AR156处理的RNA印迹分析,miR472在经过AR156处理后被下调。过量表达miR472的植物对Pst DC3000的敏感性更高。相比之下,miR472敲低的植物系则相反。转录组测序揭示了转基因植物中数千个差异表达的基因。靶标预测显示,miR472靶向许多卷曲螺旋核苷酸结合位点(NBS)和富亮氨酸重复序列(LRR)型抗性基因,并且这些靶标的表达与miR472的表达呈负相关。此外,具有剔除靶基因的转基因植物对Pst DC3000入侵的抵抗力降低。定量反转录PCR结果表明miR472的靶基因在AR156触发的ISR过程中表达。综上所述,我们的结果表明,miR472介导的沉默途径是在AR156触发的ISR期间通过NBS-LRR基因的转录后控制而发生的重要调控检查点。

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