Dunn T M, Hahn S, Ogden S, Schleif R F
Proc Natl Acad Sci U S A. 1984 Aug;81(16):5017-20. doi: 10.1073/pnas.81.16.5017.
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.
已发现一个抑制大肠杆菌araBAD操纵子所需的位点。该位点是通过缺失突变体的体内特性检测到的。用DNase I和硫酸二甲酯进行的体外保护研究表明,araC蛋白可在该区域特异性结合相对于araBAD操纵子启动子(PBAD)转录起始点位于-265至-294位的核苷酸。ara操纵子中先前已知的蛋白质结合位点位于+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位于+20至-110之间,因此位于-280的新位点沿DNA在异常长的距离上发挥其抑制作用。构建了新位点与PBAD之间插入-16、-8、0、5、11、15、24和31个碱基对的DNA。在引入DNA螺旋半圈的情况下,抑制作用受损,但对于插入0、+11和+31个碱基对,抑制作用几乎正常。