Huang Li-Fen, Lin Kuan-Hung, He Siou-Luan, Chen Jyh-Lang, Jiang Jian-Zhi, Chen Bo-Hong, Hou Yi-Syuan, Chen Ruey-Shyang, Hong Chwan-Yang, Ho Shin-Lon
Graduate School of Biotechnology and Bioengineering, Yuan Ze University, Jhongli, Taiwan.
Department of Horticulture and Biotechnology, Chinese Culture University, Taipei, Taiwan.
PLoS One. 2016 Jun 3;11(6):e0156414. doi: 10.1371/journal.pone.0156414. eCollection 2016.
An abundant 17 kDa RNase, encoded by OsPR10a (also known as PBZ1), was purified from Pi-starved rice suspension-cultured cells. Biochemical analysis showed that the range of optimal temperature for its RNase activity was 40-70°C and the optimum pH was 5.0. Disulfide bond formation and divalent metal ion Mg2+ were required for the RNase activity. The expression of OsPR10a::GUS in transgenic rice was induced upon phosphate (Pi) starvation, wounding, infection by the pathogen Xanthomonas oryzae pv. oryzae (Xoo), leaf senescence, anther, style, the style-ovary junction, germinating embryo and shoot. We also provide first evidence in whole-plant system, demonstrated that OsPR10a-overexpressing in rice and Arabidopsis conferred significant level of enhanced resistance to infection by the pathogen Xoo and Xanthomona campestris pv. campestris (Xcc), respectively. Transgenic rice and Arabidopsis overexpressing OsPR10a significantly increased the length of primary root under phosphate deficiency (-Pi) condition. These results showed that OsPR10a might play multiple roles in phosphate recycling in phosphate-starved cells and senescing leaves, and could improve resistance to pathogen infection and/or against chewing insect pests. It is possible that Pi acquisition or homeostasis is associated with plant disease resistance. Our findings suggest that gene regulation of OsPR10a could act as a good model system to unravel the mechanisms behind the correlation between Pi starvation and plant-pathogen interactions, and also provides a potential application in crops disease resistance.
从缺磷水稻悬浮培养细胞中纯化出一种由OsPR10a(也称为PBZ1)编码的丰富的17 kDa核糖核酸酶。生化分析表明,其核糖核酸酶活性的最佳温度范围为40-70°C,最佳pH值为5.0。核糖核酸酶活性需要二硫键形成和二价金属离子Mg2+。转基因水稻中OsPR10a::GUS的表达在磷酸盐(Pi)饥饿、创伤、病原菌水稻白叶枯病菌(Xanthomonas oryzae pv. oryzae,Xoo)感染、叶片衰老、花药、花柱、花柱-子房连接处、萌发胚和芽中被诱导。我们还在全株系统中首次提供证据,证明在水稻和拟南芥中过表达OsPR10a分别对病原菌Xoo和野油菜黄单胞菌野油菜致病变种(Xanthomona campestris pv. campestris,Xcc)的感染具有显著增强的抗性水平。在缺磷(-Pi)条件下,过表达OsPR10a的转基因水稻和拟南芥主根长度显著增加。这些结果表明,OsPR10a可能在缺磷细胞和衰老叶片的磷循环中发挥多种作用,并可提高对病原菌感染和/或咀嚼式害虫的抗性。磷的获取或稳态可能与植物抗病性相关。我们的研究结果表明,OsPR10a的基因调控可作为一个良好的模型系统,以揭示磷饥饿与植物-病原菌相互作用之间相关性的背后机制,也为作物抗病性提供了潜在应用。