Schmitz G, Theres K
Institut für Genetik, Universität zu Köln, Germany.
Plant J. 1994 Nov;6(5):781-6. doi: 10.1046/j.1365-313x.1994.6050781.x.
With the goal of developing a self-stabilizing transposon tagging system, a derivative of the maize transposable element Ac (Ds303) harbouring a deletion between bp 246 and 736 has been introduced into tomato (Lycopersicon esculentum) by Agrobacterium tumefaciens-mediated transformation. The deletion removes the major transcription start site, 84 bp of the putative Ac promoter and part of the untranslated leader. Transpositions from the T-DNA, where Ds303 was inserted between the mannopine synthase 1' promoter and the GUS gene, were observed in four independent transgenic plants analysed. After transposition the transposed Ds303 elements were stably integrated in the genome and could not transactivate a tester Ds element. However, somatic and germinal transpositions of the transposed Ds303 elements occurred in the presence of a transposase source.
为了开发一种自我稳定的转座子标签系统,通过根癌农杆菌介导的转化,将玉米转座元件Ac的一个衍生物(Ds303,在246至736碱基对之间存在缺失)导入番茄(Lycopersicon esculentum)。该缺失去除了主要转录起始位点、假定Ac启动子的84个碱基对以及部分非翻译前导序列。在分析的四株独立转基因植物中观察到了从T-DNA(Ds303插入甘露碱合成酶1'启动子和GUS基因之间)发生的转座。转座后,转座的Ds303元件稳定整合到基因组中,且不能激活测试Ds元件。然而,在存在转座酶来源的情况下,转座的Ds303元件发生了体细胞和生殖细胞转座。