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Global Gene Responses of Resistant and Susceptible Sugarcane Cultivars to Acidovorax avenae subsp. avenae Identified Using Comparative Transcriptome Analysis

机译:耐药和易感甘蔗品种对酸果蝇亚种的全球基因反应。使用比较转录组分析法鉴定的燕麦

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摘要

Red stripe disease in sugarcane caused by subsp. ( ) is related to serious global losses in yield. However, the underlying molecular mechanisms associated with responses of sugarcane plants to infection by this pathogen remain largely unknown. Here, we used Illumina RNA-sequencing (RNA-seq) to perform large-scale transcriptome sequencing of two sugarcane cultivars to contrast gene expression patterns of plants between and mock inoculations, and identify key genes and pathways involved in sugarcane defense responses to infection. At 0–72 hours post-inoculation (hpi) of the red stripe disease-resistant cultivar ROC22, a total of 18,689 genes were differentially expressed between -inoculated and mock-inoculated samples. Of these, 8498 and 10,196 genes were up- and downregulated, respectively. In MT11-610, which is susceptible to red stripe disease, 15,782 genes were differentially expressed between -inoculated and mock-inoculated samples and 8807 and 6984 genes were up- and downregulated, respectively. The genes that were differentially expressed following inoculation were mainly involved in photosynthesis and carbon metabolism, phenylpropanoid biosynthesis, plant hormone signal transduction, and plant–pathogen interaction pathways. Further, qRT-PCR and RNA-seq used for additional validation of 12 differentially expressed genes (DEGs) showed that eight genes in particular were highly expressed in ROC22. These eight genes participated in the biosynthesis of lignin and coumarin, as well as signal transduction by salicylic acid, jasmonic acid, ethylene, and mitogen-activated protein kinase (MAPK), suggesting that they play essential roles in sugarcane resistance to . Collectively, our results characterized the sugarcane transcriptome during early infection with , thereby providing insights into the molecular mechanisms responsible for bacterial tolerance.
机译:由亚种引起的甘蔗红色条纹病。 ()与严重的全球产量损失有关。然而,与甘蔗植物对这种病原体感染的反应相关的潜在分子机制仍然是未知的。在这里,我们使用Illumina RNA测序(RNA-seq)对两个甘蔗品种进行大规模转录组测序,以对比和模拟接种之间植物的基因表达模式,并确定涉及甘蔗对感染的防御反应的关键基因和途径。在红色条纹抗病品种ROC22接种后(hpi)0-72小时,接种样品和模拟接种样品之间共有18,689个基因差异表达。在这些基因中,分别有8498和10196个基因被上调和下调。在易患红条病的MT11-610中,接种样品和模拟接种样品之间差异表达了15782个基因,上调和下调了8807和6984个基因。接种后差异表达的基因主要涉及光合作用和碳代谢,苯丙烷生物合成,植物激素信号转导以及植物与病原体的相互作用途径。此外,用于另外验证12个差异表达基因(DEG)的qRT-PCR和RNA-seq显示,特别是八个基因在ROC22中高度表达。这8个基因参与了木质素和香豆素的生物合成,以及水杨酸,茉莉酸,乙烯和促分裂原活化蛋白激酶(MAPK)的信号转导,表明它们在甘蔗抗性中起重要作用。总的来说,我们的研究结果表征了早期感染时的甘蔗转录组,从而提供了引起细菌耐受的分子机制的见解。

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