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Identification of differentially expressed genes induced by Bamboo mosaic virus infection in Nicotiana benthamiana by cDNA-amplified fragment length polymorphism

机译:利用cDNA扩增的片段长度多态性鉴定烟草竹叶病毒感染诱导的差异表达基因

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Background The genes of plants can be up- or down-regulated during viral infection to influence the replication of viruses. Identification of these differentially expressed genes could shed light on the defense systems employed by plants and the mechanisms involved in the adaption of viruses to plant cells. Differential gene expression in Nicotiana benthamiana plants in response to infection with Bamboo mosaic virus (BaMV) was revealed using cDNA-amplified fragment length polymorphism (AFLP). Results Following inoculation with BaMV, N. benthamiana displayed differential gene expression in response to the infection. Isolation, cloning, and sequencing analysis using cDNA-AFLP furnished 90 cDNA fragments with eight pairs of selective primers. Fifteen randomly selected genes were used for a combined virus-induced gene silencing (VIGS) knockdown experiment, using BaMV infection to investigate the roles played by these genes during viral infection, specifically addressing the means by which these genes influence the accumulation of BaMV protein. Nine of the 15 genes showed either a positive or a negative influence on the accumulation of BaMV protein. Six knockdown plants showed an increase in the accumulation of BaMV, suggesting that they played a role in the resistance to viral infection, while three plants showed a reduction in coat protein, indicating a positive influence on the accumulation of BaMV in plants. An interesting observation was that eight of the nine plants showing an increase in BaMV coat protein were associated with cell rescue, defense, death, aging, signal transduction, and energy production. Conclusions This study reports an efficient and straightforward method for the identification of host genes involved in viral infection. We succeeded in establishing a cDNA-AFLP system to help track changes in gene expression patterns in N. benthamiana plants when infected with BaMV. The combination of both DNA-AFLP and VIGS methodologies made it possible to screen a large number of genes and identify those associated with infections of plant viruses. In this report, 9 of the 15 analyzed genes exhibited either a positive or a negative influence on the accumulation of BaMV in N. benthamiana plants.
机译:背景技术在病毒感染期间,植物的基因可以被上调或下调,以影响病毒的复制。这些差异表达基因的鉴定可以阐明植物所采用的防御系统以及病毒对植物细胞的适应作用所涉及的机制。利用cDNA扩增的片段长度多态性(AFLP)揭示了本氏烟草植物对竹花叶病毒(BaMV)感染的应答中的差异基因表达。结果接种BaMV后,本氏烟草显示出对感染的差异基因表达。使用cDNA-AFLP的分离,克隆和测序分析可提供90对cDNA片段,并带有八对选择性引物。将15个随机选择的基因用于病毒诱导的基因沉默(VIGS)组合击倒实验,使用BaMV感染来研究这些基因在病毒感染过程中的作用,特别是解决这些基因影响BaMV蛋白质积累的方式。 15个基因中有9个对BaMV蛋白的积累有正或负影响。六株击倒植物显示出BaMV积累的增加,表明它们在抗病毒感染中发挥了作用,而三株植物显示出外壳蛋白的减少,表明对植物中BaMV积累的积极影响。有趣的观察是,显示BaMV外壳蛋白增加的9株植物中有8株与细胞拯救,防御,死亡,衰老,信号转导和能量产生有关。结论这项研究报告了一种有效,直接的方法来鉴定与病毒感染有关的宿主基因。我们成功建立了cDNA-AFLP系统,以帮助追踪感染BaMV的本氏烟草植物中基因表达模式的变化。 DNA-AFLP和VIGS方法学的结合使筛选大量基因并鉴定与植物病毒感染相关的基因成为可能。在此报告中,分析的15个基因中有9个对本氏烟草植物中BaMV的积累表现出正或负影响。

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