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通过RNA干扰沉默一个保守且必需的根结线虫寄生基因,在转基因植物中构建广泛的根结抗性。

Engineering broad root-knot resistance in transgenic plants by RNAi silencing of a conserved and essential root-knot nematode parasitism gene.

作者信息

Huang Guozhong, Allen Rex, Davis Eric L, Baum Thomas J, Hussey Richard S

机构信息

Department of Plant Pathology, University of Georgia, Athens, GA 30602-7274, USA.

出版信息

Proc Natl Acad Sci U S A. 2006 Sep 26;103(39):14302-6. doi: 10.1073/pnas.0604698103. Epub 2006 Sep 19.

Abstract

Secreted parasitism proteins encoded by parasitism genes expressed in esophageal gland cells mediate infection and parasitism of plants by root-knot nematodes (RKN). Parasitism gene 16D10 encodes a conserved RKN secretory peptide that stimulates root growth and functions as a ligand for a putative plant transcription factor. We used in vitro and in vivo RNA interference approaches to silence this parasitism gene in RKN and validate that the parasitism gene has an essential function in RKN parasitism of plants. Ingestion of 16D10 dsRNA in vitro silenced the target parasitism gene in RKN and resulted in reduced nematode infectivity. In vivo expression of 16D10 dsRNA in Arabidopsis resulted in resistance effective against the four major RKN species. Because no known natural resistance gene has this wide effective range of RKN resistance, bioengineering crops expressing dsRNA that silence target RKN parasitism genes to disrupt the parasitic process represents a viable and flexible means of developing novel durable RKN-resistant crops and could provide crops with unprecedented broad resistance to RKN.

摘要

由在食道腺细胞中表达的寄生基因编码的分泌型寄生蛋白介导根结线虫(RKN)对植物的感染和寄生。寄生基因16D10编码一种保守的RKN分泌肽,该肽刺激根生长并作为一种假定的植物转录因子的配体发挥作用。我们使用体外和体内RNA干扰方法使RKN中的这种寄生基因沉默,并验证该寄生基因在RKN对植物的寄生中具有重要功能。在体外摄入16D10双链RNA可使RKN中的目标寄生基因沉默,并导致线虫感染性降低。在拟南芥中体内表达16D10双链RNA可产生对四种主要RKN物种有效的抗性。由于没有已知的天然抗性基因具有如此广泛有效的RKN抗性范围,因此通过生物工程改造作物,使其表达能使目标RKN寄生基因沉默以破坏寄生过程的双链RNA,是开发新型持久抗RKN作物的可行且灵活的手段,并且可以为作物提供前所未有的广泛抗RKN能力。

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