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Studies on the Expression of Sesquiterpene Synthases Using Promoter-β-Glucuronidase Fusions in Transgenic Artemisia annua L

机译:启动子-β-葡糖醛酸糖苷酶融合蛋白在转基因青蒿中表达倍半萜烯合成酶的研究

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摘要

In order to better understand the influence of sesquiterpene synthases on artemisinin yield in Artemisia annua, the expression of some sesquiterpene synthases has been studied using transgenic plants expressing promoter-GUS fusions. The cloned promoter sequences were 923, 1182 and 1510 bp for β-caryophyllene (CPS), epi-cedrol (ECS) and β-farnesene (FS) synthase, respectively. Prediction of cis-acting regulatory elements showed that the promoters are involved in complex regulation of expression. Transgenic A. annua plants carrying promoter-GUS fusions were studied to elucidate the expression pattern of the three sesquiterpene synthases and compared to the previously studied promoter of amorpha-4,11-diene synthase (ADS), a key enzyme of artemisinin biosynthesis. The CPS and ECS promoters were active in T-shaped trichomes of leaves and stems, basal bracts of flower buds and also in some florets cells but not in glandular secretory trichome while FS promoter activity was only observed in leaf cells and trichomes of transgenic shoots. ADS, CPS, ECS and FS transcripts were induced by wounding in a time depended manner. The four sesquiterpene synthases may be involved in responsiveness of A. annua to herbivory. Methyl jasmonate treatment triggered activation of the promoters of all four sesquiterpene synthases in a time depended manner. Southern blot result showed that the GUS gene was inserted into genomic DNA of transgenic lines as a single copy or two copies. The relative amounts of CPS and ECS as well as germacrene A synthase (GAS) transcripts are much lower than that of ADS transcript. Consequently, down-regulation of the expression of the CPS, ECS or GAS gene may not improve artemsinin yield. However, blocking the expression of FS may have effects on artemisinin production.
机译:为了更好地了解倍半萜合酶对青蒿中青蒿素产量的影响,已经使用表达启动子-GUS融合体的转基因植物研究了一些倍半萜合酶的表达。所克隆的启动子序列分别为β-石竹烯(CPS),表艾克多醇(ECS)和β-法呢烯(FS)合酶的923、1182和1510 bp。顺式作用调控元件的预测表明,启动子参与表达的复杂调控。研究了携带启动子-GUS融合体的转基因青蒿植物,以阐明三种倍半萜烯合酶的表达模式,并与先前研究的青蒿素生物合成关键酶无定形-4,11-二烯合酶(ADS)的启动子进行了比较。 CPS和ECS启动子在叶和茎的T形毛状体,花蕾的基片以及某些小花细胞中有活性,但在腺体分泌性毛状体中则没有活性,而FS启动子活性仅在转基因芽的叶细胞和毛状体中观察到。 ADS,CPS,ECS和FS转录本是通过按时间依赖的方式进行创伤诱导的。四种倍半萜烯合酶可能参与了农杆菌对草食动物的响应。茉莉酸甲酯处理以时间依赖的方式触发了所有四个倍半萜烯合酶的启动子的激活。 Southern印迹结果表明,GUS基因以单拷贝或两拷贝插入转基因品系的基因组DNA中。 CPS和ECS以及胚轴A合酶(GAS)转录本的相对数量要比ADS转录本的相对数量低得多。因此,CPS,ECS或GAS基因表达的下调可能不会提高青蒿素的产量。但是,阻断FS的表达可能会对青蒿素的产生产生影响。

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