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Transcriptome analysis of the compatible interaction of tomato with Verticillium dahliae using RNA-sequencing

机译:转录组分析番茄与黄萎病菌的相互作用的RNA测序

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摘要

Tomato Verticillium wilt is a soil-borne vascular disease caused by the necrotrophic fungus Verticillium dahliae. Although some understanding of plant defense mechanisms against V. dahliae infection has been gained for incompatible interactions, including identification of inducible resistant genes and defense signaling pathways, the genes and signaling pathways involved in the compatible interaction remain unclear. To investigate the molecular basis of the compatible interaction between tomato and V. dahliae, transcriptomes of V. dahliae infected tomatoes were compared to those of a control group. A total of approximately 25 million high-quality reads were generated by means of the RNA sequencing (RNA-seq) method. The sequence reads were aligned to the tomato reference genome and analyzed to measure gene expression levels, and to identify alternative splicing events. Comparative analysis between the two samples revealed 1,953 significantly differentially expressed genes (DEGs), including 1,281 up-regulated and 672 down-regulated genes. The RNA-Seq output was confirmed using RT-qPCR for 10 selected genes. The Nr, Swiss-Prot, Gene Ontology (GO), Clusters of Orthologous Groups (COG), and Kyoto Encyclopedia of Genes and Genomes (KEGG) databases were used to annotate DEG functions. Of the 1,953 DEGs identified, 1,953, 1,579, 1,739, 862, and 380 were assigned by Nr, Swiss-Prot, GO, COG, and KEGG, respectively. The important functional groups identified via GO and COG enrichment were those responsible for fundamental biological regulation, secondary metabolism, and signal transduction. Of DEGs assigned to 87 KEGG pathways, most were associated with phenylpropanoid metabolism and plant–pathogen interaction pathways. Most of the DEGs involved in these two pathways were up-regulated, and may be involved in regulating the tomato-V. dahliae compatible interaction. The results will help to identify key susceptible genes and contribute to a better understanding of the mechanisms of tomato susceptible response to V. dahliae.
机译:番茄黄萎病是一种土壤传播的血管病,由坏死性真菌大黄萎病引起。尽管对于不兼容的相互作用,包括对诱导型抗性基因和防御信号通路的鉴定,已经获得了对大丽花叶病毒感染的植物防御机制的一些理解,但尚不清楚参与兼容相互作用的基因和信号通路。为了研究番茄与大丽花弧菌之间相容相互作用的分子基础,将感染了大丽花弧菌的番茄的转录组与对照组进行了比较。通过RNA测序(RNA-seq)方法,总共产生了大约2500万个高质量读数。将序列读数与番茄参考基因组比对,并进行分析以测量基因表达水平,并鉴定其他剪接事件。两种样品之间的比较分析揭示了1,953个显着差异表达的基因(DEG),包括1,281个上调基因和672个下调基因。使用RT-qPCR确认了10个选定基因的RNA-Seq输出。使用Nr,Swiss-Prot,基因本体论(GO),直系同源簇(COG)和《京都议定书》的基因与基因组百科全书(KEGG)数据库来注释DEG功能。在确定的1,953个DEG中,分别由Nr,Swiss-Prot,GO,COG和KEGG分配了1,953、1,579、1,739、862和380。通过GO和COG富集确定的重要功能基团是负责基本生物学调节,次级代谢和信号转导的基团。在分配给87条KEGG途径的DEG中,大多数与苯丙烷代谢和植物-病原体相互作用途径有关。参与这两个途径的大多数DEGs均被上调,并可能参与了番茄V的调控。大丽花兼容的互动。该结果将有助于鉴定关键的易感基因,并有助于更好地理解番茄对大丽花弧菌的反应机制。

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