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在疫霉 RXLR 效应子的植物体内表达筛选中发现了多种表型,包括激活茄块茎抗蛋白 Rpi-blb2。

In planta expression screens of Phytophthora infestans RXLR effectors reveal diverse phenotypes, including activation of the Solanum bulbocastanum disease resistance protein Rpi-blb2.

机构信息

Department of Plant Pathology, Ohio State University-Ohio Agricultural Research and Development Center, Wooster, Ohio 44691, USA.

出版信息

Plant Cell. 2009 Sep;21(9):2928-47. doi: 10.1105/tpc.109.068247. Epub 2009 Sep 30.

Abstract

The Irish potato famine pathogen Phytophthora infestans is predicted to secrete hundreds of effector proteins. To address the challenge of assigning biological functions to computationally predicted effector genes, we combined allele mining with high-throughput in planta expression. We developed a library of 62 infection-ready P. infestans RXLR effector clones, obtained using primer pairs corresponding to 32 genes and assigned activities to several of these genes. This approach revealed that 16 of the 62 examined effectors cause phenotypes when expressed inside plant cells. Besides the well-studied AVR3a effector, two additional effectors, PexRD8 and PexRD36(45-1), suppressed the hypersensitive cell death triggered by the elicitin INF1, another secreted protein of P. infestans. One effector, PexRD2, promoted cell death in Nicotiana benthamiana and other solanaceous plants. Finally, two families of effectors induced hypersensitive cell death specifically in the presence of the Solanum bulbocastanum late blight resistance genes Rpi-blb1 and Rpi-blb2, thereby exhibiting the activities expected for Avrblb1 and Avrblb2. The AVRblb2 family was then studied in more detail and found to be highly variable and under diversifying selection in P. infestans. Structure-function experiments indicated that a 34-amino acid region in the C-terminal half of AVRblb2 is sufficient for triggering Rpi-blb2 hypersensitivity and that a single positively selected AVRblb2 residue is critical for recognition by Rpi-blb2.

摘要

爱尔兰马铃薯晚疫病病原菌致病疫霉预计会分泌数百种效应蛋白。为了解决将计算预测的效应基因赋予生物学功能的挑战,我们结合了等位基因挖掘和高通量的活体表达。我们开发了一个包含 62 个感染准备就绪的 P. infestans RXLR 效应克隆的文库,该文库是使用对应于 32 个基因的引物对获得的,并为其中的几个基因分配了活性。这种方法揭示了在植物细胞内表达的 62 个受检效应物中的 16 个会引起表型。除了研究充分的 AVR3a 效应物外,另外两个效应物 PexRD8 和 PexRD36(45-1),抑制了由 P. infestans 的另一种分泌蛋白 INF1 触发的过敏细胞死亡。一个效应物 PexRD2,在 Nicotiana benthamiana 和其他茄科植物中促进细胞死亡。最后,两个效应物家族在存在 Solanum bulbocastanum 晚疫病抗性基因 Rpi-blb1 和 Rpi-blb2 的情况下,特异性地诱导过敏细胞死亡,从而表现出 Avrblb1 和 Avrblb2 的预期活性。然后更详细地研究了 AVRblb2 家族,发现它在 P. infestans 中高度变异且受到多样化选择的影响。结构功能实验表明,AVRblb2 中 C 端半部分的 34 个氨基酸区域足以触发 Rpi-blb2 过敏反应,并且 AVRblb2 中的一个单一正选择残基对于 Rpi-blb2 的识别至关重要。

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