首页> 外文期刊>Plant Cell, Tissue and Organ Culture: An International Journal on in Vitro Culture of Higher Plants >Overexpression of the chestnut CsTL1 gene coding for a thaumatin-like protein in somatic embryos of Quercus robur
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Overexpression of the chestnut CsTL1 gene coding for a thaumatin-like protein in somatic embryos of Quercus robur

机译:板栗CsTL1基因编码丘陵体体胚中的一种奇异蛋白类似蛋白的过表达。

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摘要

Somatic embryos of Quercus robur derived from mature and juvenile trees were transformed with the CsTL1 gene coding for an antifungal protein. Clumps of somatic embryos were inoculated with Agrobacterium tumefaciens strain EHA105 harbouring a binary vector (pKWG2D-TAU) that included the green fluorescence protein (GFP) reporter gene. After 24 weeks of culture on selective medium, significantly higher transformation frequencies were obtained in a temporary immersion system (TIS) than in semi-solid medium (ranging from 1.4 to 9.6 % for the four genotypes). The first transformants appeared after 10 weeks and GFP activity was evaluated in all kan-resistant embryogenic lines. The transgenic nature of lines was confirmed by PCR and Southern blotting. CsTL1 transcripts were detected in all transgenic lines (TL) analyzed by quantitative real-time PCR, and levels of expression were significantly higher than in the wild type (wt), reaching up to 24 times higher in some genotypes. Sixty-two stable TL were obtained (38 derived from centenarian trees). Plant conversion rates of transformed somatic embryos were similar to those of the wt and were increased by use of the TIS. GFP fluorescence was detected in roots and shoots of transgenic plants, which confirmed stable transformation of regenerants.
机译:用编码抗真菌蛋白的CsTL1基因转化来自成熟树和幼树的栎的体细胞胚。用具有二元载体(pKWG2D-TAU)的根癌农杆菌菌株EHA105接种体细胞胚块,该二元载体包括绿色荧光蛋白(GFP)报道基因。在选择性培养基上培养24周后,在临时浸没系统(TIS)中获得的转化频率明显高于在半固体培养基中(四种基因型在1.4%至9.6%的范围内)。第一个转化体在10周后出现,并在所有对kan具有抗性的胚胎发生系中评估GFP活性。通过PCR和Southern印迹证实了品系的转基因性质。在所有实时定量PCR分析的转基因品系(TL)中均检测到CsTL1转录本,其表达水平显着高于野生型(wt),在某些基因型中表达水平高达24倍。获得了62个稳定的TL(38个来自百岁老人树)。转化的体细胞胚的植物转化率与野生型相似,并通过使用TIS得以提高。在转基因植物的根和芽中检测到GFP荧光,这证实了再生体的稳定转化。

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