Adachi T, Mizuuchi K, Menzel R, Gellert M
Nucleic Acids Res. 1984 Aug 24;12(16):6389-95. doi: 10.1093/nar/12.16.6389.
We have determined the sequence of a 1498 base-pair region in E. coli that extends from within dnaN through recF and into the gyrB gene. An open reading frame of 1071 base pairs has been identified with the recF structural gene. By S1 mapping, we have located a transcription start point 31 base pairs upstream of gyrB. The amount of this transcript is much greater in cells that have been treated with novobiocin, a treatment which is known to induce greater synthesis of DNA gyrase.
我们已经确定了大肠杆菌中一段1498个碱基对区域的序列,该区域从dnaN内部延伸至recF并进入gyrB基因。已鉴定出一个与recF结构基因相关的1071个碱基对的开放阅读框。通过S1图谱分析,我们在gyrB上游31个碱基对处定位到一个转录起始点。在用新生霉素处理的细胞中,这种转录本的量要多得多,已知新生霉素处理可诱导更多的DNA促旋酶合成。