College of Horticulture, Northwest A & F University, Yangling 712100, Shaanxi, PR China.
J Exp Bot. 2011 Nov;62(15):5671-82. doi: 10.1093/jxb/err253. Epub 2011 Aug 23.
RING finger proteins comprise a large family and play important roles in regulation of growth and development, hormone signalling, and responses to biotic and abiotic stresses in plants. In this study, the identification and functional characterization of a C4C4-type RING finger protein gene from the Chinese wild grapevine Vitis pseudoreticulata (designated VpRFP1) are reported. VpRFP1 was initially identified as an expressed sequence tag (EST) from a cDNA library constructed from leaves of V. pseudoreticulata inoculated with the grapevine powdery mildew Uncinula necator. Sequence analysis of the deduced VpRFP1 protein based on the full-length cDNA revealed an N-terminal nuclear localization signal (NLS) and a C-terminal C4C4-type RING finger motif with the consensus sequence Cys-X(2)-Cys-X(13)-Cys-X(1)-Cys-X(4)-Cys-X(2)-Cys-X(10)-Cys-X(2)-Cys. Upon inoculation with U. necator, expression of VpRFP1 was rapidly induced to higher levels in mildew-resistant V. pseudoreticulata plants. In contrast, expression of VpRFP1 was down-regulated in mildew-susceptible V. vinifera plants. Western blotting using an antibody raised against VpRFP1 showed that VpRFP1 was also induced to higher levels in V. pseudoreticulata plants at 12-48 hours post-inoculation (hpi). However, there was only slight increase in VpRFP in V. vinifera plants in the same time frame, even though a more significant increase was observed at 96-144 hpi in these plants. Results from transactivation assays in yeast showed that the RING finger motif of VpRFP1 exhibited some activity of transcriptional activation; however, no activity was seen with the full-length VpRFP1. Overexpression of VpRFP1 in Arabidopsis plants was found to enhance resistance to Arabidopsis powdery mildew Golovinomyces cichoracearum, which seemed to be correlated with increased transcript levels of AtPR1 and AtPR2 in the pathogen-infected tissues. In addition, the Arabidopsis transgenic lines showed enhanced resistance to a virulent bacterial pathogen Pseudomonas syringae pv. tomato DC3000. Taken together, the results suggested that VpRFP1 may be a transcriptional activator of defence-related genes in grapevines.
环指蛋白家族是一个庞大的家族,在植物的生长发育、激素信号转导以及生物和非生物胁迫响应中发挥着重要作用。本研究从中国野生葡萄(Vitis pseudoreticulata) cDNA 文库中鉴定并对一个 C4C4 型环指蛋白基因(VpRFP1)进行了功能表征,该基因是从接种葡萄白粉病病原菌 Uncinula necator 的葡萄叶片 cDNA 文库中获得的一个表达序列标签(EST)。根据全长 cDNA 序列分析,VpRFP1 蛋白含有一个 N 端核定位信号(NLS)和一个 C 端 C4C4 型环指结构域,其保守序列为 Cys-X(2)-Cys-X(13)-Cys-X(1)-Cys-X(4)-Cys-X(2)-Cys-X(10)-Cys-X(2)-Cys。接种 U. necator 后,在抗白粉病的 V. pseudoreticulata 植株中,VpRFP1 的表达迅速诱导至更高水平。相比之下,在感白粉病的 V. vinifera 植株中,VpRFP1 的表达被下调。用针对 VpRFP1 蛋白的抗体进行 Western blotting 分析表明,接种后 12-48 小时,V. pseudoreticulata 植株中 VpRFP1 的诱导水平也更高。然而,在相同时间范围内,V. vinifera 植株中 VpRFP 的含量仅略有增加,尽管在这些植株中,96-144 hpi 时观察到了更显著的增加。酵母中转录激活实验的结果表明,VpRFP1 的环指结构域具有一定的转录激活活性,但全长 VpRFP1 没有活性。在拟南芥植物中过表达 VpRFP1 发现,其增强了拟南芥白粉病 Golovinomyces cichoracearum 的抗性,这似乎与感染组织中 AtPR1 和 AtPR2 的转录本水平升高有关。此外,拟南芥转基因株系对一种毒力较强的细菌病原体丁香假单胞菌 pv. tomato DC3000 表现出增强的抗性。综上所述,结果表明 VpRFP1 可能是葡萄中防御相关基因的转录激活因子。