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Cloning and functional analysis of the promoters that upregulate carotenogenic gene expression during flower development in Gentiana lutea

机译:秦ent花发育过程中上调致龋基因表达的启动子的克隆与功能分析

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Over the last two decades, many carotenogenic genes have been cloned and used to generate metabolically engineered plants producing higher levels of carotenoids. However, comparatively little is known about the regulation of endogenous carotenogenic genes in higher plants, and this restricts our ability to predict how engineered plants will perform in terms of carotenoid content and composition. During petal development in the Great Yellow Gentian (Gentiana lutea), carotenoid accumulation, the formation of chromoplasts and the upregulation of several carotenogenic genes are temporally coordinated. We investigated the regulatory mechanisms responsible for this coordinated expression by isolating five G. lutea carotenogenic gene (GlPDS, GlZDS, GlLYCB, GlBCH and GlLYCE) promoters by inverse polymerase chain reaction (PCR). Each promoter was sufficient for developmentally regulated expression of the gusA reporter gene following transient expression in tomato (Solanum lycopersicum cv. Micro-Tom). Interestingly, the GlLYCB and GlBCH promoters drove high levels of gusA expression in chromoplast-containing mature green fruits, but low levels in chloroplast-containing immature green fruits, indicating a strict correlation between promoter activity, tomato fruit development and chromoplast differentiation. As well as core promoter elements such as TATA and CAAT boxes, all five promoters together with previously characterized GlZEP promoter contained three common cis-regulatory motifs involved in the response to methyl jasmonate (CGTCA) and ethylene (ATCTA), and required for endosperm expression (Skn-1_motif, GTCAT). These shared common cis-acting elements may represent binding sites for transcription factors responsible for co-regulation. Our data provide insight into the regulatory basis of the coordinated upregulation of carotenogenic gene expression during flower development in G. lutea.
机译:在过去的二十年中,已经克隆了许多类胡萝卜素基因,并用于生成代谢工程化的植物,从而产生更高水平的类胡萝卜素。但是,对高​​等植物中内源性类胡萝卜素基因的调控知之甚少,这限制了我们根据类胡萝卜素含量和组成预测工程化植物表现的能力。在大黄龙胆(Gentiana lutea)的花瓣发育过程中,类胡萝卜素的积累,叶绿体的形成和几种类胡萝卜素基因的上调在时间上是协调的。我们通过逆聚合酶链反应(PCR)分离了五个G.lutea类胡萝卜素基因(GlPDS,GlZDS,GlLYCB,GlBCH和GlLYCE)启动子,研究了负责这种协调表达的调控机制。在番茄中短暂表达后,每个启动子足以用于gusA报告基因的发育调控表达(Solanum lycopersicum cv。Micro-Tom)。有趣的是,GlLYCB和GlBCH启动子在含有色体的成熟绿色水果中驱动了高水平的gusA表达,而在含有叶绿体的未成熟绿色水果中却降低了gusA表达,表明启动子活性,番茄果实发育与色体分化之间存在严格的相关性。以及核心启动子元件(例如TATA和CAAT盒),所有五个启动子以及先前表征的GlZEP启动子都包含三个常见的顺式调控基序,参与了对茉莉酸甲酯(CGTCA)和乙烯(ATCTA)的反应,并且是胚乳表达所必需的(Skn-1_motif,GTCAT)。这些共有的共同的顺式作用元件可以代表负责共调节的转录因子的结合位点。我们的数据提供了对G. lutea花发育过程中类胡萝卜素基因表达协同上调的调控基础的见解。

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