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Improvement of Strawberry Fruit Softening through the Silencing of Cell Wall Genes

机译:通过细胞壁基因沉默的草莓果实软化的改进

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To improve strawberry fruit shelf life, we have analyzed the effect of inhibiting the expression of several ripening-specific cell wall genes through antisense or RNAi transformation. The down-regulation of the genes FaplC and FaPG1 encoding a pectate lyase and a polygalacturonase enzyme, respectively, notably reduced the loss of firmness at the red ripe stage. Interestingly, PG-silenced plants showed firmer fruits than pectate lyase plants. In co transformation experiments with Agrobacterium strains carrying both genes, we found that several transgenic lines yielded firmer fruits than plants transformed with PG or pectate lyase alone, indicating a possible synergistic effect of both pectolytic enzymes on cell wall disassembly. Contrary to these results, the inhibition of the genes related to xyloglucan processing and/or depolymerization FaEG3 and FaExp2, encoding a β-1,4-glucanase and an expansin protein, respectively, did not modify fruit softening. A high number of FaExp2-silenced plants showed significant phenotypic alterations which could be related to the role of this gene in cell expansion. Currently, we are evaluating strawberry plants transformed with antisense sequences of a β-galactosidase and an acetyl pectin esterase gene, the product of both genes acting on the pectin matrix. Globally, our investigations show that it is possible to modify strawberry fruit softening through the inhibition of genes involved in pectin processing.
机译:为了提高草莓果实保质期,我们已经分析了通过反义或RNAI转化抑制若干成熟特异性细胞壁基因表达的效果。分别对宫内裂解酶和多糖酶酶的基因FaplC和FAPG1的下调分别显着降低了红色成熟阶段的固体损失。有趣的是,PG沉默的植物显示出比果胶酶植物更坚固的水果。在携带两个基因的农杆菌菌株的共同转化实验中,我们发现,几种转基因系比用PG或果胶酶转化的植物单独产生更高的果实,表明两种果胶酶对细胞壁拆卸的可能协同作用。与这些结果相反,分别抑制与木糖葡聚糖加工和/或解聚Faeg3和Faexp2相关的基因,分别编码β-1,4-葡聚糖酶和扩张蛋白,未改变果实软化。大量的Faexp2沉默的植物显示出显着的表型改变,其可能与该基因在细胞膨胀中的作用有关。目前,我们正在评估用β-半乳糖苷酶的反义序列和乙酰果胶酯酶基因转化的草莓植物,这两个基因作用于果胶基质的产物。在全球范围内,我们的研究表明,通过抑制果胶加工中涉及的基因可以改变草莓果实软化。

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