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Cloning of a Nicotiana plumbaginifolia protoplast-specific enhancer-like sequence

机译:烟草李原生质体特异性增强子样序列的克隆

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摘要

We have isolated a 1.5-kb plant DNA fragment (called insert 7) from Nicotiana plumbaginifolia DNA that contains a protoplast-specific enhancer-like sequence. The presence of this sequence on a plasmid carrying a chimeric nos-npt-II gene conferring kanamycin resistance to plant cells, produces an overexpression of the npt-II gene during at least eight days after protoplast transformation. This effect on the expression of the nos promoter was independent of the orientation and was observed both on circular and linearized plasmids. On the contrary, insert 7 had no influence when present on another plasmid (in trans) in cotransformation experiments. The overexpression of the nos-npt-II gene due to the presence of insert 7 on the transforming plasmid is correlated with a higher level of synthesis of the corresponding RNA. Insert 7 did not affect the level of expression of the nos-npt-II gene in stably transformed calli, or in regenerated plants. However, the overexpression was again detected in protoplasts prepared from leaves of stably transformed plants. This 1.5-kb plant DNA fragment contains highly repetitive DNA sequences, specific to N. plumbaginifolia. However, the enhancer-like activity is localized on a 600-bp unique sequence of insert 7. Insert 7 had no detectable effect on the transient expression of another gene, the nopaline synthase gene present at a longer distance on the same plasmid.
机译:我们从烟草李子烟草DNA中分离了一个1.5 kb的植物DNA片段(称为插入片段7),其中含有原生质体特异的增强子样序列。在携带对植物细胞具有卡那霉素抗性的嵌合nos-npt-II基因的质粒上,该序列的存在会在原生质体转化后至少八天之内产生npt-II基因的过表达。这种对nos启动子表达的影响与方向无关,并且在环状和线性质粒上均可以观察到。相反,在共转化实验中,插入物7存在于另一质粒(反式)时没有影响。由于在转化质粒上存在插入物7,nos-npt-II基因的过表达与相应RNA的更高合成水平相关。插入物7在稳定转化的愈伤组织或再生植物中不影响nos-npt-II基因的表达水平。然而,在从稳定转化的植物的叶片制备的原生质体中再次检测到过表达。这个1.5 kb的植物DNA片段包含高度重复的DNA序列,特异于李子猪笼草。但是,增强子样活性位于插入物7的600 bp唯一序列上。插入物7对另一个基因的瞬时表达没有可检测到的影响,胭脂碱合酶基因在同一质粒上的距离较长。

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