Nomura T, Aiba H, Ishihama A
J Biol Chem. 1985 Jun 10;260(11):7122-5.
The transcriptional organization was determined for the DNA polymerase III epsilon subunit (dnaQ) and the ribonuclease H (rnh) genes, which are closely spaced and organized in a face-to-face system (Maki, H., Horiuchi, T., and Sekiguchi, M. (1983) Proc. Natl. Acad. Sci. U. S. A. 80, 7137-7141). Nuclease S1 mapping revealed that transcription starts from a single promoter for rnh and two promoters for dnaQ and proceeds in opposite directions. The 5' terminus of the rnh RNA overlaps about 100 and 20 nucleotide sequences with the 5' terminus of the dnaQ-1 and dnaQ-2 RNA, respectively. The levels of in vivo transcription for the three RNA species increased altogether by more than 10-fold in cells carrying a multicopy plasmid with intact dnaQ-rnh genes, keeping the relative level for the convergent transcription units nearly constant.
已确定了DNA聚合酶IIIε亚基(dnaQ)和核糖核酸酶H(rnh)基因的转录组织,这两个基因紧密相邻,并以面对面的方式排列(牧木,H.,堀内,T.,和关口,M.(1983年)《美国国家科学院院刊》80,7137 - 7141)。核酸酶S1图谱分析表明,转录从rnh的一个单一启动子以及dnaQ的两个启动子起始,并向相反方向进行。rnh RNA的5'末端分别与dnaQ - 1和dnaQ - 2 RNA的5'末端重叠约100和20个核苷酸序列。在携带含有完整dnaQ - rnh基因的多拷贝质粒的细胞中,这三种RNA的体内转录水平总共增加了10倍以上,同时保持了趋同转录单元的相对水平几乎恒定。