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Identification Validation and Utilization of Novel Nematode-Responsive Root-Specific Promoters in Arabidopsis for Inducing Host-Delivered RNAi Mediated Root-Knot Nematode Resistance

机译:鉴定验证和利用新型线虫反应的根特定启动子在拟南芥中诱导宿主传递RNAi介导的根结线虫抗性。

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摘要

The root-knot nematode (RKN), Meloidogyne incognita, is an obligate, sedentary endoparasite that infects a large number of crops and severely affects productivity. The commonly used nematode control strategies have their own limitations. Of late, RNA interference (RNAi) has become a popular approach for the development of nematode resistance in plants. Transgenic crops capable of expressing dsRNAs, specifically in roots for disrupting the parasitic process, offer an effective and efficient means of producing resistant crops. We identified nematode-responsive and root-specific (NRRS) promoters by using microarray data from the public domain and known conserved cis-elements. A set of 51 NRRS genes was identified which was narrowed down further on the basis of presence of cis-elements combined with minimal expression in the absence of nematode infection. The comparative analysis of promoters from the enriched NRRS set, along with earlier reported nematode-responsive genes, led to the identification of specific cis-elements. The promoters of two candidate genes were used to generate transgenic plants harboring promoter GUS constructs and tested in planta against nematodes. Both promoters showed preferential expression upon nematode infection, exclusively in the root in one and galls in the other. One of these NRRS promoters was used to drive the expression of splicing factor, a nematode-specific gene, for generating host-delivered RNAi-mediated nematode-resistant plants. Transgenic lines expressing dsRNA of splicing factor under the NRRS promoter exhibited upto a 32% reduction in number of galls compared to control plants.
机译:根结线虫(RKN)是一种隐性的久坐的寄生虫,它会感染大量农作物并严重影响生产力。常用的线虫控制策略有其自身的局限性。最近,RNA干扰(RNAi)已成为发展植物线虫抗性的流行方法。能够表达dsRNA的转基因农作物,特别是在根部表达干扰杂草过程的农作物,是生产抗性农作物的有效途径。我们通过使用来自公共领域和已知保守的顺式元件的微阵列数据,鉴定了线虫反应性和根特异性(NRRS)启动子。鉴定出一组51个NRRS基因,该基因在不存在线虫感染的情况下,由于顺式元素的存在与最小表达的结合而进一步缩小。来自丰富的NRRS集的启动子与早期报道的线虫反应性基因的启动子的比较分析导致了特定顺式元件的鉴定。使用两个候选基因的启动子来生成带有启动子GUS构建体的转基因植物,并在植物中针对线虫进行了测试。两种启动子在线虫感染后均显示优先表达,仅在一个的根部,而在另一个的根部。使用这些NRRS启动子之一来驱动剪接因子(一种线虫特异性基因)的表达,以生成宿主递送的RNAi介导的耐线虫植物。与对照植物相比,在NRRS启动子下表达剪接因子dsRNA的转基因品系显示出高达32%的胆汁减少。

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