首页> 外文期刊>Plant Molecular Biology >A Catharanthus roseus BPF-1 homologue interacts with an elicitor-responsive region of the secondary metabolite biosynthetic gene Str and is induced by elicitor via a JA-independent signal transduction pathway
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A Catharanthus roseus BPF-1 homologue interacts with an elicitor-responsive region of the secondary metabolite biosynthetic gene Str and is induced by elicitor via a JA-independent signal transduction pathway

机译:长春花BPF-1同源物与次级代谢产物生物合成基因Str的激发子响应区域相互作用,并由激发子通过独立于JA的信号转导途径诱导

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摘要

Plants respond to pathogen attack by induction of various defence responses, including the biosynthesis of protective secondary metabolites. In Catharanthus roseus, the elicitor-induced expression of the terpenoid indole alkaloid biosynthetic gene Strictosidine synthase (Str) is mediated via the plant stress hormone jasmonate. In the promoters of several defence-related genes, cis-acting elements have been identified that are important for transcriptional regulation upon stress signals. Here we show that an upstream region in the Str promoter confers responsiveness to partially purified yeast elicitor and jasmonate. Yeast one-hybrid screening with this element as a bait identified a MYB-like protein, which shows high homology to parsley box P-binding factor-1 (PcBPF-1). In vitro analyses showed that the Str promoter fragment contained a novel binding site for BPF-1-like proteins with higher binding affinity than the previously described box P. CrBPF-1 mRNA accumulated rapidly in elicitor-treated C. roseus suspension cells, whereas no induction was observed with jasmonate. Inhibitor studies indicated that CrBPF-1 plays a role in an elicitor-responsive but jasmonate-independent signal transduction pathway, acting downstream of protein phosphorylation and calcium influx. [References: 31]
机译:植物通过诱导各种防御反应(包括保护性次生代谢产物的生物合成)来对病原体攻击做出反应。在长春花中,引发剂诱导的萜类吲哚生物碱生物合成基因Strictosidine合酶(Str)的表达是通过植物胁迫激素茉莉酸酯介导的。在几个与防御相关的基因的启动子中,已确定了顺式作用元件,对应激信号的转录调控很重要。在这里,我们显示了Str启动子中的上游区域赋予了对部分纯化的酵母激发子和茉莉酸酯的响应性。酵母以该元件为诱饵进行一次杂交筛选,鉴定出一种MYB样蛋白,该蛋白与欧芹盒P结合因子1(PcBPF-1)具有高度同源性。体外分析表明,Str启动子片段含有BPF-1类蛋白的新结合位点,其结合亲和力高于先前描述的盒形P。CrBPF-1mRNA在激发子处理的玫瑰假丝酵母悬浮细胞中迅速积累,而没有茉莉酸诱导诱导。抑制剂研究表明,CrBPF-1在激发子响应但与茉莉酸酯无关的信号转导途径中起作用,作用于蛋白磷酸化和钙内流的下游。 [参考:31]

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