首页> 外文期刊>The Plant Cell >In Planta Expression Screens of Phytophthora infestans RXLR Effectors Reveal Diverse Phenotypes, Including Activation of the Solanum bulbocastanum Disease Resistance Protein Rpi-blb2.
【24h】

In Planta Expression Screens of Phytophthora infestans RXLR Effectors Reveal Diverse Phenotypes, Including Activation of the Solanum bulbocastanum Disease Resistance Protein Rpi-blb2.

机译:在疫霉菌RXLR效应器的植物表达筛选中,揭示了多种表型,包括球茎茄抗病蛋白Rpi-blb2的激活。

获取原文
获取原文并翻译 | 示例
           

摘要

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, 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.
机译:预计爱尔兰马铃薯饥荒病原体疫霉疫霉会分泌数百种效应蛋白。为了解决将生物学功能分配给计算预测的效应子基因的挑战,我们将等位基因挖掘与植物表达中的高通量相结合。我们开发了一个库,其中包含62个已准备好感染的P. infestans RXLR效应子克隆,该克隆使用对应于32个基因的引物对获得,并为其中一些基因分配了活性。该方法揭示了在植物细胞内表达时,在62种受检查的效应子中有16种会引起表型。除了经过充分研究的AVR3a效应子外,另外两个效应子PexRD8和PexRD36还抑制了由致病疫霉的另一种分泌蛋白elicitin INF1触发的超敏细胞死亡。一种效应物,PexRD2,促进了本氏烟草和其他茄科植物的细胞死亡。最后,两个效应子家族特别是在茄果晚疫病抗性基因Rpi-blb1和Rpi-blb2的存在下诱导了超敏细胞死亡,从而展现了Avrblb1和Avrblb2预期的活性。然后,对AVRblb2家族进行了更详细的研究,发现其变异性很高,并且在感染晚疫病菌中处于多样化选择之下。结构功能实验表明,AVRblb2 C端一半的34个氨基酸区域足以触发Rpi-blb2超敏反应,单个阳性选择的AVRblb2残基对于Rpi-blb2的识别至关重要。

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号