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Creation of elite growth and development features in PAP1-programmed red Nicotiana tabacum Xanthi via overexpression of synthetic geranyl pyrophosphate synthase genes

机译:通过合成的长甲基焦磷酸合成酶基因的过表达,在PAP1编程的红色尼古塔塔纳氏蛋白Xanthi中创建精英增长和开发特征

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We report effects of overexpression of synthetic cDNAs encoding two forms of geranyl pyrophosphate synthase (GPPS) on growth and development performance of Production of Anthocyanin Pigment 1 (PAP1) gene-programmed tobacco (Nicotiana tabacum Xanthi) plants. Isogenic PAP1-programmed tobacco plants have a new trait that highly expresses anthocyanin biosynthetic pathway in all plant tissues, thus being considered a novel material for different studies. We recently used a homomeric Myzus persicae GPPS (MpGPPS) cDNA as a template to synthesize two new cDNA forms, sMpGPPS-HA and PTP-sMpGPPS-HA, which were designed to localize encoded proteins in the cytosol and plastids, respectively. One binary construct containing sMpGPPS-HA, the other binary construct containing PTP-sMpGPPS-HA, and another control construct were introduced to PAP1-programmed plants, respectively. Twenty to twenty-two T0 plants were generated for each construct. Seeds were collected from all plants to select T1 progeny with one single copy of the transgenes. Based on the Mendel law of inheritance, four T0 lines for each construct were identified to contain one single copy of transgene. A large number of T1 progeny from these T0 plants were selected for evaluation of plant development performance. The resulting data showed that the overexpression of each synthetic cDNA significantly enhanced fast growth, increased internodes and leaf numbers, increased leaf sizes, promoted earlier flowering, and approximately doubled plant biomass. This study indicates that a simultaneous enhancement of plant anthocyanin and terpenoid pathways creates novel elite PAP1-programmed plant varieties.
机译:我们报告了编码两种形式的焦磷酸合酶(GPPS)的合成CDNA过表达对花青素的生长和发育性能的影响,对花青素素颜料1(PAP1)基因编程的烟草(Nicotiana Tabacum Xanthi)植物产生的生长和发育性能。 Isogenic PAP1编程的烟草植物具有新的特征,在所有植物组织中高度表达了花青素生物合成途径,因此被认为是不同研究的新型材料。我们最近使用了均匀的Myzus persicae gpps(mpgpps)cDNA作为模板,以合成两种新的cDNA形式,SMPGPPS-HA和PTP-SMPGPPS-HA,它们分别设计用于将编码的蛋白质定位在细胞溶胶和体层中。含有SMPGPPS-HA的一个二元构建体,分别引入PAP1编程植物的PPG-SMPGPPS-HA的其他二元构建体,以及另一个对照构建体。为每个构建体产生二十到二十二个T0植物。从所有植物中收集种子以用一份转基因的单一拷贝选择T1后代。基于孟德尔的遗传法,鉴定了每个构建体的四条T0线,含有一拷贝的转基因。选择来自这些T0植物的大量T1后代,用于评估植物开发性能。得到的数据显示,每个合成cDNA的过表达显着增强了快速增长,增加的间面和叶数,增加的叶片尺寸,促进的开花,大约一倍的植物生物质。该研究表明,植物的同时增强花青素和萜烯型途径会产生新的精英PAP1编程植物品种。

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