Shiba K, Mizobuchi K
Department of Biophysics and Biochemistry, Faculty of Science, University of Tokyo, Japan.
J Bacteriol. 1990 Apr;172(4):1992-7. doi: 10.1128/jb.172.4.1992-1997.1990.
The replication frequency of plasmid ColIb-P9 depends on the level of repZ gene expression, which is negatively regulated by the action of the inc gene (C. Hama, T. Takizawa, H. Moriwaki, Y. Urasaki, and K. Mizobuchi, J. Bacteriol. 172:1983-1991, 1990). To further understand the mechanism of this regulation, we analyzed transcripts of the ColIb-P9 replication control region. Four RNA species, designated RNAI to RNAIV, were observed in plasmid pCH11, which contained the whole inc gene region and the 5' portion of the repZ gene. RNAII, RNAIII, and RNAIV, with sizes of approximately 200, 500, and 1,500 bases, respectively, were identified as rightward transcripts that shared common transcription initiation sites; RNAIV was determined to be equivalent to a part of repZ mRNA, which was observed in pCH10, a plasmid that contained sufficient information for replication and control of ColIb-P9. Conversely, RNAI, with a size of about 70 bases, was transcribed leftward and was identified as the product of the inc gene and hence equivalent to inc RNA detected by in vitro RNA synthesis. This small RNA was found to be complementary to a part of repZ mRNA. These results and quantitative analyses of the transcripts in Inc- mutants indicate that the inc RNA negatively regulates repZ expression mainly at the posttranscriptional level through the possible formation of an inc RNA-repZ mRNA hybrid in the host cells.
质粒ColIb - P9的复制频率取决于repZ基因的表达水平,而inc基因的作用对其表达具有负调控作用(C. 滨名、泷泽彻、森胁博、浦崎洋和沟渊和男,《细菌学杂志》172:1983 - 1991,1990年)。为了进一步了解这种调控机制,我们分析了ColIb - P9复制控制区的转录本。在含有完整inc基因区域和repZ基因5'端部分的质粒pCH11中观察到四种RNA分子,分别命名为RNAI至RNAIV。RNAII、RNAIII和RNAIV的大小分别约为200、500和1500个碱基,它们被鉴定为具有共同转录起始位点的向右转录本;RNAIV被确定等同于repZ mRNA的一部分,在质粒pCH10中观察到了repZ mRNA,pCH10含有ColIb - P9复制和控制的足够信息。相反,大小约为70个碱基的RNAI向左转录,被鉴定为inc基因的产物,因此等同于通过体外RNA合成检测到的inc RNA。发现这种小RNA与repZ mRNA的一部分互补。这些结果以及对Inc - 突变体中转录本的定量分析表明,inc RNA主要在转录后水平通过在宿主细胞中可能形成inc RNA - repZ mRNA杂交体来负调控repZ的表达。