Zhang Lei, Davies Laura J, Elling Axel A
Department of Plant Pathology, Washington State University, Pullman, WA, 99164, USA.
Mol Plant Pathol. 2015 Jan;16(1):48-60. doi: 10.1111/mpp.12160. Epub 2014 Jun 30.
Root-knot nematodes are sedentary biotrophic endoparasites that maintain a complex interaction with their host plants. Nematode effector proteins are synthesized in the oesophageal glands of nematodes and secreted into plant tissue through a needle-like stylet. Effectors characterized to date have been shown to mediate processes essential for nematode pathogenesis. To gain an insight into their site of action and putative function, the subcellular localization of 13 previously isolated Meloidogyne incognita effectors was determined. Translational fusions were created between effectors and EGFP-GUS (enhanced green fluorescent protein-β-glucuronidase) reporter genes, which were transiently expressed in tobacco leaf cells. The majority of effectors localized to the cytoplasm, with one effector, 7H08, imported into the nuclei of plant cells. Deletion analysis revealed that the nuclear localization of 7H08 was mediated by two novel independent nuclear localization domains. As a result of the nuclear localization of the effector, 7H08 was tested for the ability to activate gene transcription. 7H08 was found to activate the expression of reporter genes in both yeast and plant systems. This is the first report of a plant-parasitic nematode effector with transcriptional activation activity.
根结线虫是定居型活体营养内寄生生物,与寄主植物保持着复杂的相互作用。线虫效应蛋白在其食管腺中合成,并通过针状口针分泌到植物组织中。迄今已鉴定出的效应蛋白已被证明介导线虫致病过程中必不可少的过程。为了深入了解它们的作用位点和假定功能,确定了13种先前分离的南方根结线虫效应蛋白的亚细胞定位。在效应蛋白与EGFP-GUS(增强型绿色荧光蛋白-β-葡萄糖醛酸酶)报告基因之间构建翻译融合体,并在烟草叶细胞中瞬时表达。大多数效应蛋白定位于细胞质,其中一个效应蛋白7H08被导入植物细胞核中。缺失分析表明,7H08的核定位由两个新的独立核定位域介导。由于效应蛋白的核定位,对7H08激活基因转录的能力进行了测试。发现7H08在酵母和植物系统中均能激活报告基因的表达。这是关于具有转录激活活性的植物寄生线虫效应蛋白的首次报道。