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Factors Affecting the Level of Kanamycin Resistance in Transformed Sunflower Cells

机译:影响转化向日葵细胞卡那霉素抗性水平的因素

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摘要

A 230 base pair DNA segment containing the sequences 5′ to the 700 to 750 nucleotide (nt) transcript 7′ (ORF 3; RF Barker, KB Idler, DV Thompson, JD Kemp 1983 Plant Mol Biol 2: 335-350) of the octopine tumor inducing plasmid pTiA6 has been isolated. This region has (a) 180 base pairs of DNA upstream of the TATA box, (b) the start of RNA synthesis, and (c) the entire 5′ untranslated region of the gene. We have fused this presumed promoter fragment to the neomycin phosphotransferase II (NPTII) gene from Tn5 in a plant expression cassette. After recombination into a tumor inducing plasmid delivery plasmid, this cassette confers selectable kanamycin resistance to transformed sunflower cells. Removal of the out-of-frame ATG in the 5′ leader sequence of the NPTII gene by two different modifications increased both the levels of NPTII enzyme activity and the ID50 for kanamycin in the tumor cells. The promoter region of the transcript 7 gene gives levels of kanamycin resistance equivalent to the nopaline synthase promoter and octopine synthase promoter when used in the same constructions and assayed in the same tissues.
机译:一个230个碱基对的DNA片段,其中包含700-750个核苷酸(nt)转录本7'的序列5'(ORF 3; RF Barker,KB Idler,DV Thompson,JD Kemp 1983 Plant Mol Biol 2:335-350)。已分离出章鱼碱诱导肿瘤的质粒pTiA6。该区域在TATA盒上游具有(a)180个碱基对的DNA,(b)RNA合成的开始,以及(c)基因的整个5'非翻译区。我们已经将这种推测的启动子片段与植物表达盒中来自Tn5的新霉素磷酸转移酶II(NPTII)基因融合。在重组为肿瘤诱导质粒递送质粒后,该盒赋予转化的向日葵细胞选择性的卡那霉素抗性。通过两种不同的修饰去除NPTII基因的5'前导序列中的框外ATG,既增加了肿瘤细胞中NPTII酶活性的水平,又增加了卡那霉素的ID50。当在相同的结构中使用并在相同的组织中进行检测时,转录本7基因的启动子区域可提供相当于胭脂碱合酶启动子和章鱼碱合酶启动子的卡那霉素抗性水平。

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