Laboratoire de Biologie et Pathologie Végétales, Université de Nantes, IFR 149 QUASAV, EA 1157, 2 rue de la Houssinière, BP 92208, 44322 Nantes Cedex 3, France.
Mol Plant Pathol. 2011 Sep;12(7):638-52. doi: 10.1111/j.1364-3703.2010.00702.x. Epub 2011 Feb 17.
Phelipanche ramosa L. parasitizes major crops, acting as a competitive sink for host photoassimilates, especially sucrose. An understanding of the mechanisms of sucrose utilization in parasites is an important step in the development of new control methods. Therefore, in this study, we characterized the invertase gene family in P. ramosa and analysed its involvement in plant development. Invertase-encoded cDNAs were isolated using degenerate primers corresponding to highly conserved regions of invertases. In addition to enzyme assays, gene expression was analysed using real-time quantitative reverse transcriptase-polymerase chain reaction during overall plant development. The dominant isoform was purified and sequenced using electrospray ionization-liquid chromatography-tandem mass spectrometry (ESI-LC-MS/MS). Five invertase-encoded cDNAs were thus characterized, including PrSai1 which encodes a soluble acid invertase (SAI). Of the five invertases, PrSai1 transcripts and SAI activity were dominant in growing organs. The most active invertase corresponded to the PrSai1 gene product. The purified PrSAI1 displayed low pI and optimal pH values, specificity for β-fructofuranosides and inhibition by metallic ions and competitive inhibition by fructose. PrSAI1 is a typical vacuolar SAI that is actively involved in growth following both germination and attachment to host roots. In addition, germinated seeds displayed enhanced cell wall invertase activity (PrCWI) in comparison with preconditioned seeds, suggesting the contribution of this activity in the sink strength of infected roots during the subsequent step of root penetration. Our results show that PrSAI1 and, possibly, PrCWI constitute good targets for the development of new transgenic resistance in host plants using proteinaceous inhibitors or silencing strategies.
肉苁蓉寄生主要农作物,作为宿主光合产物,尤其是蔗糖的竞争性汇。了解寄生植物中蔗糖利用的机制是开发新的控制方法的重要步骤。因此,在这项研究中,我们鉴定了肉苁蓉中的转化酶基因家族,并分析了其在植物发育中的作用。使用对应于转化酶高度保守区域的简并引物分离转化酶编码 cDNA。除了酶测定外,还使用实时定量逆转录聚合酶链反应在整个植物发育过程中分析基因表达。使用电喷雾电离-液相色谱-串联质谱(ESI-LC-MS/MS)对主要同工型进行纯化和测序。因此,鉴定了 5 个转化酶编码 cDNA,包括编码可溶性酸性转化酶(SAI)的 PrSai1。在这 5 种转化酶中,PrSai1 转录物和 SAI 活性在生长器官中占主导地位。最活跃的转化酶对应于 PrSai1 基因产物。纯化的 PrSAI1 显示出低等电点和最佳 pH 值,对β-呋喃果糖苷具有特异性,并受到金属离子的抑制和果糖的竞争性抑制。PrSAI1 是一种典型的液泡 SAI,在发芽后和附着在宿主根部后都能积极参与生长。此外,与预处理种子相比,发芽种子显示出增强的细胞壁转化酶活性(PrCWI),这表明在随后的根穿透步骤中,感染根的汇强度中存在这种活性。我们的结果表明,PrSAI1 和可能的 PrCWI 可能成为使用蛋白质抑制剂或沉默策略在宿主植物中开发新的转基因抗性的良好靶标。