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首页> 外文期刊>Scientific reports. >Comparison of regeneration capacity and Agrobacterium-mediated cell transformation efficiency of different cultivars and rootstocks of Vitis spp. via organogenesis
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Comparison of regeneration capacity and Agrobacterium-mediated cell transformation efficiency of different cultivars and rootstocks of Vitis spp. via organogenesis

机译:葡萄不同品种和砧木的再生能力和农杆菌介导的细胞转化效率的比较。通过器官发生

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The success of in vitro plant regeneration and the competence of genetic transformation greatly depends on the genotype of the species of interest. In previous work, we developed a method for the efficient Agrobacterium-mediated genetic transformation via organogenesis of V. vinifera cultivar Thompson Seedless, by using meristematic bulk (MB) as starting tissue. In this study, we applied this method for the regeneration and transformation of MBs obtained from the Italian cultivar Ciliegiolo and two of the commonly used Vitis rootstocks, 110 Richter and Kober 5BB, in comparison with Thompson Seedless. The A. tumefaciens strain EHA105, harbouring pK7WG2 binary vector, was used for the transformation trials, which allowed selection through the enhanced-green fluorescent protein (eGFP) and the neomycin phosphotransferase (nptII) gene. Putative transformed tissues and/or shoots were identified by either a screening based on the eGFP expression alone or its use in combination with kanamycin in the medium. MBs obtained from Thompson Seedless showed the highest regeneration and transformation cell competence, which subsequently allowed the recovery of stably transformed plants. Ciliegiolo, 110 Richter, and Kober 5BB, produced actively growing transgenic calli showing eGFP fluorescence, more consistently on selective media, but had no regenerative competence.
机译:体外植物再生的成功和遗传转化的能力在很大程度上取决于目标物种的基因型。在以前的工作中,我们通过使用分生组织块(MB)作为起始组织,开发了一种有效的农杆菌介导的遗传转化方法,该方法是通过葡萄栽培种汤普森无核的器官发生来进行的。在这项研究中,与Thompson Seedless相比,我们将这种方法应用于从意大利品种Ciliegiolo和两种常用的Vitis砧木110 Richter和Kober 5BB中获得的MBs的再生和转化。使用带有pK7WG2二元载体的根癌农杆菌EHA105进行转化试验,该试验允许通过增强的绿色荧光蛋白(eGFP)和新霉素磷酸转移酶(nptII)基因进行选择。通过仅基于eGFP表达的筛选或将其与卡那霉素联合使用在培养基中来鉴定推定的转化组织和/或芽。从Thompson Seedless获得的MB表现出最高的再生和转化细胞能力,随后可以回收稳定转化的植物。 Ciliegiolo,110 Richter和Kober 5BB产生了活跃生长的转基因愈伤组织,在选择培养基上更一致地显示eGFP荧光,但没有再生能力。

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