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首页> 外文期刊>Plant Growth Regulation: An International Journal on Natural and Synthetic Regulators >Influence of calcium influx induced by the calcium ionophore, A23187, on resveratrol content and the expression of CDPK and STS genes in the cell cultures of Vitis amurensis
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Influence of calcium influx induced by the calcium ionophore, A23187, on resveratrol content and the expression of CDPK and STS genes in the cell cultures of Vitis amurensis

机译:钙离子载体A23187诱导的钙内流对紫葡萄细胞培养物中白藜芦醇含量及CDPK和STS基因表达的影响

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The present study examines the effect of calcium influx induced by the calcium ionophore (CI) on the biosynthesis of resveratrol and the expression of stilbene synthase (STS) and calcium-dependent protein kinase (CDPK) genes in cell cultures of Vitis amurensis, which have different levels of resveratrol production. The present study utilized the control cell culture V2 of V. amurensis, which contains no more than 0. 02 % dry weight (DW) of resveratrol, in addition to rolB transgenic cell cultures VB1 and VB2, which have increased resveratrol contents (0. 1-0. 8 % DW). Treatment with the CI at a 1 μM concentration significantly increased STS gene expression (6 of 10 analyzed STS genes) and resveratrol production in the control V2 cell culture by fourfold; however, use of the CI at 10 μM significantly decreased resveratrol production by 2-4 fold in all cell cultures tested. In the control V2 grape cell culture, treatment with the CI increased expression of all of the CDPK genes except VaCDPK1a and VaCDPK3a. In the rolB transgenic VB2 grape cell culture treated with the CI, we detected alterations in expression of several CDPK genes, but these changes in gene expression were not significant. Our results indicated that treatment with 1 μM of the CI increased resveratrol content and production in control grape cells by selectively increasing the expression of STS genes. Conversely, the CI treatment did not significantly increase resveratrol content and production, or the expression of CDPK or STS genes in the rolB transgenic cells. Likely, untreated VB2 cells have increased concentrations of cytoplasmic calcium, and therefore, treatment with the CI did not significantly change CDPK expression. These results suggest that the rolB gene has an important role in the regulation of calcium-dependent transduction pathways in transformed cells.
机译:本研究研究了钙离子载体(CI)诱导的钙内流对白藜芦醇生物合成以及葡萄细胞培养中二苯乙烯合成酶(STS)和钙依赖性蛋白激酶(CDPK)基因表达的影响。白藜芦醇生产水平不同。本研究利用了V. amurensis的对照细胞培养物V2,其中含有不超过0. 02%干重(DW)的白藜芦醇,以及rolB转基因细胞培养物VB1和VB2,其白藜芦醇含量增加(0。 1-0。8%DW)。用浓度为1μM的CI处理可将对照V2细胞培养物中的STS基因表达(10个分析的STS基因中的6个)显着增加4倍;但是,在所有测试的细胞培养物中,使用10μM的CI会显着降低白藜芦醇的产量2-4倍。在对照V2葡萄细胞培养物中,用CI处理可以增加除VaCDPK1a和VaCDPK3a以外的所有CDPK基因的表达。在用CI处理的rolB转基因VB2葡萄细胞培养物中,我们检测到了几种CDPK基因表达的变化,但这些基因表达的变化并不显着。我们的结果表明,通过选择性增加STS基因的表达,用1μM的CI处理可增加对照葡萄细胞中白藜芦醇的含量和产量。相反,CI处理并没有显着增加白藜芦醇的含量和产量,或rolB转基因细胞中CDPK或STS基因的表达。可能的是,未经处理的VB2细胞具有增加的细胞质钙浓度,因此,用CI处理不会显着改变CDPK表达。这些结果表明,rolB基因在转化细胞中钙依赖性转导途径的调控中具有重要作用。

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