首页> 美国卫生研究院文献>Proceedings of the National Academy of Sciences of the United States of America >An operator at -280 base pairs that is required for repression of araBAD operon promoter: addition of DNA helical turns between the operator and promoter cyclically hinders repression.
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An operator at -280 base pairs that is required for repression of araBAD operon promoter: addition of DNA helical turns between the operator and promoter cyclically hinders repression.

机译:抑制araBAD操纵子启动子所需的-280个碱基对的操纵子:在操纵子和启动子之间添加DNA螺旋匝会周期性地抑制阻遏。

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摘要

A site has been found that is required for repression of the Escherichia coli araBAD operon. This site was detected by the in vivo properties of deletion mutants. In vitro protection studies with DNase I and dimethylsulfate showed that araC protein can specifically bind in this area to nucleotides lying at position -265 to -294 with respect to the araBAD operon promoter (PBAD) transcription start point. The previously known sites of protein binding in the ara operon lie between +20 and -160. Since the properties of deletion strains show that all the sites required for araBAD induction lie between +20 and -110, the new site at -280 exerts its repressive action over an unusually large distance along the DNA. Insertions of -16, -8, 0, 5, 11, 15, 24, and 31 base pairs of DNA between the new site and PBAD were constructed. Repression was impaired in those cases in which half-integral turns of the DNA helix were introduced, but repression was nearly normal for the insertions of 0, +11, and +31 base pairs.
机译:已经发现抑制大肠杆菌araBAD操纵子所需的位点。通过缺失突变体的体内特性检测到该位点。 DNase I和硫酸二甲酯的体外保护研究表明,araC蛋白可以在该区域特异性结合相对于araBAD操纵子启动子(PBAD)转录起点-265至-294的核苷酸。 ara操纵子中蛋白质结合的先前已知位点在+20至-160之间。由于缺失菌株的特性表明,araBAD诱导所需的所有位点都在+20至-110之间,因此-280处的新位点在沿着DNA的异常大的距离内发挥着抑制作用。构建了在新位点和PBAD之间插入-16,-8、0、5、11、15、24和31个碱基对的DNA。在引入DNA螺旋的半整数圈的情况下,抑制作用减弱,但是插入0,+ 11和+31个碱基对时,抑制作用几乎是正常的。

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