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利用瞬时 GUS 表达开发猕猴桃的农杆菌介导基因转移系统。

The use of transient GUS expression to develop an Agrobacterium-mediated gene transfer system for kiwifruit.

机构信息

Centre for Gene Technology, University of Auckland, Private Bag, Auckland, New Zealand.

出版信息

Plant Cell Rep. 1993 Nov;13(1):28-31. doi: 10.1007/BF00232310.

Abstract

We have monitored transient GUS expression 4-5 days after cocultivation of leaf explants with Agrobacterium, in order to optimise parameters of cocultivation and so develop an efficient, reproducible gene transfer system in kiwifruit. Factors that were important included the health of the explant, the strain of Agrobacterium, and the binary vector used. Pre-culture of the leaf explants before cocultivation inhibited gene transfer at the cut edge. Placing the explants on moist filter paper during cocultivation gave increased frequencies of gene transfer. Stably transformed, kanamycin-resistant plants were obtained at good frequency from the optimised system. PCR and Southern analysis of the regenerated plants confirmed their transgenic nature.

摘要

我们已经监测到叶外植体与农杆菌共培养 4-5 天后瞬时 GUS 表达,以优化共培养参数,从而在猕猴桃中开发高效、可重复的基因转移系统。重要的因素包括外植体的健康状况、农杆菌菌株和使用的二元载体。共培养前对外植体的预培养抑制了切口边缘的基因转移。在共培养过程中外植体放在湿润的滤纸上增加了基因转移的频率。从优化的系统中以良好的频率获得了稳定转化、卡那霉素抗性的植物。再生植株的 PCR 和 Southern 分析证实了它们的转基因性质。

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