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Combinatorial expression of transcription factor genes B-Peru and mPAP1 enhances anthocyanin accumulation in transgenic Petunia hybrid

机译:转录因子基因B-Peru和mPAP1的组合表达增强了转基因矮牵牛杂种中的花色苷积累

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The present study aimed to determine the role of transcription factors (bHLH and MYB) in enhancing anthocyanin production in Petunia 'Mirage rose'. Initially, we optimized an Agrobacterium-mediated transformation protocol to over-express transcription factors (B-Peru, mPAP1, and B-Peru + mPAP1) in Petunia. Phosphinothricin (PPT) concentrations of 0.5, 1.0, and 1.5 mg l(-1) were found to be ideal for the selection and regeneration of transformed shoots at different developmental stages. Clavamox (250 mg l(-1)) efficiently eliminated Agrobacterium after co-cultivation (2 days) and favored maximum shoot regeneration. In addition, incubation for 30 min in Agrobacterium suspension increased the number of transformed cells and resulted in improved regeneration in the selection medium. The transformed plants were successfully developed through a direct organogenesis system. The transformed plants were selected using BASTA (R) and the presence of transgenes was assessed using PCR. Visible anthocyanin accumulation was evident only in plantlets (shoots, stem, leaves, and roots) carrying the gene combination B-Peru + mPAP1. The expression of biosynthetic genes involved in the flavonoid pathway was analyzed using quantitative real-time PCR. Expression levels of PAL, CHS, CHI, F3H, DFR, and ANS were higher in the young and mature leaves of plants transformed with B-Peru + mPAP1 compared to those transformed with B-Peru, mPAP1, and/or non-transformed plants. Furthermore, the highest level of anthocyanin was recorded in the leaves, stem, and roots of plants transformed with B-Peru + mPAP1. These results validate the combinatorial requirement of B-Peru and mPAP1 to enhance anthocyanin content in Petunia hybrida 'Mirage rose'. (C) 2016 Elsevier B.V. All rights reserved.
机译:本研究旨在确定转录因子(bHLH和MYB)在矮牵牛“海市rose楼”花色苷生产中的作用。最初,我们优化了农杆菌介导的转化协议,以在矮牵牛中过表达转录因子(B-Peru,mPAP1和B-Peru + mPAP1)。发现浓度分别为0.5、1.0和1.5 mg l(-1)的膦丝菌素(PPT)非常适合选择和再生处于不同发育阶段的转化芽。共培养(2天)后,Clavamox(250 mg l(-1))有效消除了土壤杆菌,并有利于最大芽再生。此外,在农杆菌悬浮液中孵育30分钟可增加转化细胞的数量,并改善选择培养基中的再生。通过直接的器官发生系统成功地开发了转化的植物。使用BASTA选择转化的植物,并使用PCR评估转基因的存在。仅在携带基因组合B-Peru + mPAP1的小植株(芽,茎,叶和根)中可见花青素积聚。使用定量实时PCR分析了类黄酮途径中的生物合成基因的表达。与用B-Peru,mPAP1和/或未转化植物转化的植物相比,用B-Peru + mPAP1转化的植物的幼叶和成熟叶中PAL,CHS,CHI,F3H,DFR和ANS的表达水平更高。此外,在用B-Peru + mPAP1转化的植物的叶子,茎和根中,花青素的含量最高。这些结果证实了B-Peru和mPAP1的组合要求以增强矮牵牛'Mirage rose'中花色苷的含量。 (C)2016 Elsevier B.V.保留所有权利。

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