Promoter analysis of the rice stemar-13-ene synthase gene OsDTC2, which is involved in the biosynthesis of the phytoalexin oryzalexin S

Tadahiro Nemoto , Atsushi Okada , Kazunori Okada , Naoto Shibuya , Tomonobu Toyomasu , Hideaki Nojiri , Hisakazu Yamane
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引用次数: 6

Abstract

A rice diterpene cyclase, OsDTC2, functions as a stemar-13-ene synthase that converts syn-copalyl diphosphate into stemar-13-ene, a putative diterpene hydrocarbon precursor of the phytoalexin oryzalexin S. The transcriptional expression of OsDTC2 is induced by treatment of suspension-cultured rice cells with a chitin oligosaccharide elicitor. To investigate the molecular mechanisms of the elicitor signaling pathway that leads to OsDTC2 expression, we carried out deletion and mutation analysis of the region − 1939 bp upstream of the transcription start site of OsDTC2 in rice cells using dual luciferase assays. The region between − 1709 and − 1450 bp was found to contain six W-box motifs, which are putative recognition sites for WRKY transcription factors, as cis elements involved in elicitor-responsiveness and/or basic promoter activity of OsDTC2.

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水稻茎秆13烯合成酶基因OsDTC2的启动子分析,该基因参与植物抗菌素oryzalexin S的生物合成
水稻二萜环化酶OsDTC2是一种茎-13-烯合成酶,可将syn-copalyl二磷酸转化为茎-13-烯,这是植物抗菌素oryzalexin s的一种假定的二萜碳氢化合物前体。用几丁质寡糖激发子处理悬浮液培养的水稻细胞可诱导OsDTC2的转录表达。为了研究引发OsDTC2表达的启动子信号通路的分子机制,我们使用双荧光素酶法对水稻细胞中OsDTC2转录起始位点上游- 399bp的区域进行了缺失和突变分析。在- 1709和- 1450 bp之间的区域发现了6个W-box基序,这些基序是WRKY转录因子的假定识别位点,作为参与OsDTC2的启动子响应性和/或基本启动子活性的顺式元件。
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