Irdani T, Bogani P, Mengoni A, Mastromei G, Buiatti M
Istituto Sperimentale per la Zoologia Agraria, Ministero delle Politiche Agricole, Cascine del Riccio, Florence, Italy.
Plant Mol Biol. 1998 Aug;37(6):1079-84. doi: 10.1023/a:1006082815434.
A new binary vector encoding for Candida albicans dihydrofolate reductase (DFR1) has been constructed and used as a dominant selectable marker for plant transformation. Transgenic tobacco plants with an increased resistance to methotrexate (Mtx) were obtained by co-transformation of tobacco leaf discs with Agrobacterium tumefaciens strains carrying two new binary vectors: pTI20 and pTI18. Co-transformants of Nicotiana tabacum were directly selected for and rooted on medium containing both kanamycin (kan) and Mtx. Leaf discs of transgenic plants were assayed for capacity of regeneration at different Mtx concentrations. Analysis of transcripts was performed on total RNA extracted from two Mtx-resistant plants. The transgenic plants increased resistance to Mtx can be explained by the exceptionally low capacity of Mtx to bind C. albicans dihydrofolate reductase, accountable by the presence of two amino acid residues strategically important in Mtx binding.
一种编码白色念珠菌二氢叶酸还原酶(DFR1)的新型二元载体已构建完成,并用作植物转化的显性选择标记。通过将烟草叶盘与携带两种新型二元载体pTI20和pTI18的根癌农杆菌菌株共转化,获得了对甲氨蝶呤(Mtx)抗性增强的转基因烟草植株。直接在含有卡那霉素(kan)和Mtx的培养基上选择并使烟草共转化体生根。测定了转基因植物叶盘在不同Mtx浓度下的再生能力。对从两株抗Mtx植物中提取的总RNA进行了转录本分析。转基因植物对Mtx抗性增强的原因可能是Mtx与白色念珠菌二氢叶酸还原酶的结合能力极低,这是由在Mtx结合中具有重要战略意义的两个氨基酸残基的存在所导致的。