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黄花龙胆花发育过程中上调类胡萝卜素生成基因表达的启动子的克隆与功能分析

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

作者信息

Zhu Changfu, Yang Qingjie, Ni Xiuzhen, Bai Chao, Sheng Yanmin, Shi Lianxuan, Capell Teresa, Sandmann Gerhard, Christou Paul

机构信息

School of Life Sciences, Changchun Normal University, Changchun, 130032, China; Departament de Producció Vegetal i Ciència Forestal, Universitat de Lleida-Agrotecnio Center, Lleida, 25198, Spain.

出版信息

Physiol Plant. 2014 Apr;150(4):493-504. doi: 10.1111/ppl.12129. Epub 2013 Dec 27.

Abstract

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.

摘要

在过去二十年中,许多类胡萝卜素生成基因已被克隆,并用于培育能够产生更高水平类胡萝卜素的代谢工程植物。然而,关于高等植物内源性类胡萝卜素生成基因的调控,我们所知相对较少,这限制了我们预测工程植物在类胡萝卜素含量和组成方面表现的能力。在大黄龙胆(Gentiana lutea)花瓣发育过程中,类胡萝卜素积累、质体的形成以及几个类胡萝卜素生成基因的上调在时间上是协调的。我们通过反向聚合酶链反应(PCR)分离出五个大黄龙胆类胡萝卜素生成基因(GlPDS、GlZDS、GlLYCB、GlBCH和GlLYCE)的启动子,研究了负责这种协调表达的调控机制。在番茄(Solanum lycopersicum cv. Micro-Tom)中瞬时表达后,每个启动子都足以驱动gusA报告基因的发育调控表达。有趣的是,GlLYCB和GlBCH启动子在含有质体的成熟绿色果实中驱动gusA高水平表达,但在含有叶绿体的未成熟绿色果实中驱动低水平表达,这表明启动子活性、番茄果实发育和质体分化之间存在严格的相关性。除了TATA和CAAT框等核心启动子元件外,所有五个启动子与先前表征的GlZEP启动子一起,都含有三个共同的顺式调控基序,这些基序参与茉莉酸甲酯(CGTCA)和乙烯(ATCTA)响应,并且是胚乳表达所必需的(Skn-1_motif,GTCAT)。这些共享的共同顺式作用元件可能代表负责协同调控的转录因子的结合位点。我们的数据为大黄龙胆花发育过程中类胡萝卜素生成基因表达协调上调的调控基础提供了见解。

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