首页> 美国卫生研究院文献>Nucleic Acids Research >Complex formation of nuclear proteins with the RNA polymerase I promoter and repeated elements in the external transcribed spacer of Cucumis sativus ribosomal DNA.
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Complex formation of nuclear proteins with the RNA polymerase I promoter and repeated elements in the external transcribed spacer of Cucumis sativus ribosomal DNA.

机译:核蛋白与RNA聚合酶I启动子和黄瓜黄瓜核糖体DNA外部转录间隔区中的重复元件的复合物形成。

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摘要

Complex repetitive structures are located downstream of the transcription initiation site in the intergenic spacer (IGS) of the rRNA genes in Cucumis sativus (cucumber). In order to show that these repetitive elements of the 5'external transcribed spacer (ETS) are probably involved in transcriptional regulation as protein binding sites DNA-protein binding assays were carried out. The same proteins that recognize two binding sites in the promoter region analysed (upstream binding element between -164 and -105, and core promoter between -41 and +16) show binding affinity to the complex structures of the 5'external transcribed spacer. These proteins also seem to interact with the single strands of the respective DNA regions suggesting an effect on transcriptional regulation while the DNA is transcribed and, therefore, is single-stranded. Three proteins were isolated by affinity column chromatography; these proteins turned out to be much smaller (16, 22, and 24 kDa, respectively) than promoter and enhancer binding proteins in animal systems. Additionally, a 70-kDa protein could be characterized cooperating with a small segment of the repeated elements but not with the promoter.
机译:复杂的重复结构位于黄瓜(Cucumis sativus)(黄瓜)中rRNA基因的基因间隔区(IGS)中转录起始位点的下游。为了显示5'外部转录间隔区(ETS)的这些重复元件可能参与了蛋白质结合位点的转录调控,因此进行了DNA-蛋白质结合测定。识别分析的启动子区域中两个结合位点的相同蛋白质(-164和-105之间的上游结合元件,-41和+16之间的核心启动子)对5'外部转录间隔区的复杂结构具有结合亲和力。这些蛋白质似乎也与各个DNA区域的单链相互作用,表明在转录DNA并因此为单链时对转录调控产生影响。通过亲和柱色谱法分离出三种蛋白质。这些蛋白比动物系统中的启动子和增强子结合蛋白要小得多(分别为16、22和24 kDa)。另外,可以表征70-kDa的蛋白质与重复元件的一小段合作而不与启动子合作。

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