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首页> 外文期刊>The Indian journal of genetics & plant breeding >Characterization of root-knot nematode responsive and root-specific promoter containing PIN domain from Arabidopsis thaliana (L.) Heynh.
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Characterization of root-knot nematode responsive and root-specific promoter containing PIN domain from Arabidopsis thaliana (L.) Heynh.

机译:来自拟南芥(L.)Heynh的含有PIN结构域的根结线虫响应和根特异性启动子的表征。

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摘要

Root-knot nematodes (Meloidogyne incognita) are obligate plant parasites, causing significant economic loss, that alter expression of host genes in order to establish and maintain their feeding sites in the roots of host plants. In the present study, a nematode-responsive-root-specific gene (AT1G26530) was identified which expressed in roots of Arabidopsis thaliana after nematode infection. Quantitative RT-PCR analysis of this gene revealed maximum (similar to 2.58 fold) up-regulation at 21 days post inoculation of nematode. A 1580 bp region upstream of the translational start site of AT1G26530 was isolated and transformed into Arabidopsis through floral dip method. On analysis of Arabidopsis transgenic plants harboring AT1G26530 prm::GUS fusion, reporter gene expression was seen exclusively in galls after nematode inoculation. Interestingly, strong GUS activity was observed at early stages of nematode infection, starting from 14 days and was sustained up to 30 days post inoculation. Furthermore, 85 to 93 % galls exhibited GUS activity in the nematode feeding sites. The specificity of the activity of the AT1G26530 promoter, in terms of nematode-responsiveness and root specificity, makes it a suitable candidate to express dsRNA of nematode genes and engineer plants with resistance against root-knot nematodes using HD-RNAi technology.
机译:根结线虫(Meloidogyne incognita)是专性的植物寄生虫,会造成重大的经济损失,从而改变宿主基因的表达,从而在宿主植物的根部建立并维持它们的取食位点。在本研究中,鉴定出线虫反应根特异性基因(AT1G26530),该基因在线虫感染后在拟南芥的根中表达。对该基因进行的定量RT-PCR分析显示,在接种线虫后21天,其最大上调(约2.58倍)。分离了AT1G26530翻译起始位点上游的1580bp区域,并通过花浸法将其转化为拟南芥。在分析携带AT1G26530 prm :: GUS融合蛋白的拟南芥转基因植物时,线虫接种后仅在胆汁中观察到报告基因表达。有趣的是,在线虫感染的早期阶段,从14天开始观察到很强的GUS活性,并在接种后持续30天。此外,在线虫摄食部位,有85%至93%的胆汁表现出GUS活性。就线虫应答性和根系特异性而言,AT1G26530启动子活性的特异性使其成为表达线虫基因的dsRNA并使用HD-RNAi技术改造对根结线虫具有抗性的植物的合适候选者。

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