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

被引:37
作者
Kiselev, K. V. [1 ,2 ]
Shumakova, O. A. [1 ,2 ]
Manyakhin, A. Y. [3 ]
Mazeika, A. N. [2 ]
机构
[1] Russian Acad Sci, Far Eastern Branch, Inst Biol & Soil Sci, Biotechnol Lab, Vladivostok 690022, Russia
[2] Far Eastern Fed Univ, Dept Biochem & Biotechnol, Vladivostok 690090, Russia
[3] Russian Acad Sci, Far Eastern Branch, Mt Taiga Stn, Primorsky Krai 692533, Ussuriisky Regi, Russia
基金
俄罗斯基础研究基金会;
关键词
Calcium ionophore; Callus culture; CDPK; Resveratrol; STS; Vitis amurensis; PHENYLALANINE AMMONIA-LYASE; STILBENE SYNTHASE GENES; SUSPENSION CULTURES; PROTEIN-KINASE; PANAX-GINSENG; PHYTOALEXIN RESVERATROL; MOLECULAR ANALYSIS; TRANS-RESVERATROL; ONCOGENE ROLB; ACCUMULATION;
D O I
10.1007/s10725-012-9725-z
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
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 mu M 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 mu M 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 mu M 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.
引用
收藏
页码:371 / 381
页数:11
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