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Transcriptome Analysis Highlights Defense and Signaling Pathways Mediated by Rice pi21 Gene with Partial Resistance to Magnaporthe oryzae

机译:转录组分析凸显了水稻对稻瘟病菌具有部分抗性的pi21基因介导的防御和信号传导途径

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摘要

Rice blast disease is one of the most destructive rice diseases worldwide. The pi21 gene confers partial and durable resistance to Magnaporthe oryzae. However, little is known regarding the molecular mechanisms of resistance mediated by the loss-of-function of Pi21. In this study, comparative transcriptome profiling of the Pi21-RNAi transgenic rice line and Nipponbare with M. oryzae infection at different time points (0, 12, 24, 48, and 72 hpi) were investigated using RNA sequencing. The results generated 43,222 unique genes mapped to the rice genome. In total, 1109 differentially expressed genes (DEGs) were identified between the Pi21-RNAi line and Nipponbare with M. oryzae infection, with 103, 281, 209, 69, and 678 DEGs at 0, 12, 24, 48, and 72 hpi, respectively. Functional analysis showed that most of the DEGs were involved in metabolism, transport, signaling, and defense. Among the genes assigned to plant—pathogen interaction, we identified 43 receptor kinase genes associated with pathogen-associated molecular pattern recognition and calcium ion influx. The expression levels of brassinolide-insensitive 1, flagellin sensitive 2, and elongation factor Tu receptor, ethylene (ET) biosynthesis and signaling genes, were higher in the Pi21-RNAi line than Nipponbare. This suggested that there was a more robust PTI response in Pi21-RNAi plants and that ET signaling was important to rice blast resistance. We also identified 53 transcription factor genes, including WRKY, NAC, DOF, and ERF families that show differential expression between the two genotypes. This study highlights possible candidate genes that may serve a function in the partial rice blast resistance mediated by the loss-of-function of Pi21 and increase our understanding of the molecular mechanisms involved in partial resistance against M. oryzae.
机译:稻瘟病是世界上最具破坏性的稻病之一。 pi21基因赋予了对稻瘟病菌部分和持久的抗性。然而,关于由Pi21的功能丧失介导的抗性的分子机制知之甚少。在这项研究中,使用RNA测序技术研究了Pi21-RNAi转基因水稻品系和日本米粉在不同时间点(0、12、24、48和72 hpi)感染米曲霉的比较转录组谱。结果产生了映射到水稻基因组的43,222个独特基因。在Pi21-RNAi品系和米巴霉菌感染的日本晴之间共鉴定出1109个差异表达基因(DEG),分别在0、12、24、48和72 hpi时分别具有103、281、209、69和678个DEG。 , 分别。功能分析表明,大多数DEG参与代谢,转运,信号传导和防御。在分配给植物与病原体相互作用的基因中,我们鉴定了43种与病原体相关的分子模式识别和钙离子流入有关的受体激酶基因。 Pi21-RNAi系中,油菜素内酯不敏感1,鞭毛蛋白敏感2和延伸因子Tu受体,乙烯(ET)的生物合成和信号转导基因的表达水平高于日本晴。这表明在Pi21-RNAi植物中PTI反应更为强烈,而ET信号对于稻瘟病抗性很重要。我们还确定了53个转录因子基因,包括WRKY,NAC,DOF和ERF家族,它们在两种基因型之间表现出差异表达。这项研究突出了可能的候选基因,这些基因可能在Pi21功能丧失介导的部分稻瘟病抗性中起作用,并增加了我们对参与部分抗稻瘟病菌的分子机制的理解。

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