Hiraga S, Sugiyama T, Itoh T
Department of Biology, Faculty of Science, Osaka University, Japan.
J Bacteriol. 1994 Dec;176(23):7233-43. doi: 10.1128/jb.176.23.7233-7243.1994.
The incA gene product of ColE2-P9 and ColE3-CA38 plasmids is an antisense RNA that regulates the production of the plasmid-coded Rep protein essential for replication. The Rep protein specifically binds to the origin and synthesizes a unique primer RNA at the origin. The IncB incompatibility is due to competition for the Rep protein among the origins of the same binding specificity. We localized the regions sufficient for autonomous replication of 15 ColE plasmids related to ColE2-P9 and ColE3-CA38 (ColE2-related plasmids), analyzed their incompatibility properties, and determined the nucleotide sequences of the replicon regions of 9 representative plasmids. The results suggest that all of these plasmids share common mechanisms for initiation of DNA replication and its control. Five IncA specificity types, 4 IncB specificity types, and 9 of the 20 possible combinations of the IncA and IncB types were found. The specificity of interaction of the Rep proteins and the origins might be determined by insertion or deletion of single nucleotides and substitution of several nucleotides at specific sites in the origins and by apparently corresponding insertion or deletion and substitution of amino acid sequences at specific regions in the C-terminal portions of the Rep proteins. For plasmids of four IncA specificity types, the nine-nucleotide sequences at the loop regions of the stem-loop structures of antisense RNAs are identical, suggesting an evolutionary significance of the sequence. The mosaic structures of the replicon regions with homologous and nonhomologous segments suggest that some of them were generated by exchanging functional parts through homologous recombination.
ColE2 - P9和ColE3 - CA38质粒的incA基因产物是一种反义RNA,它调节质粒编码的复制所必需的Rep蛋白的产生。Rep蛋白特异性结合到复制起点,并在复制起点合成一种独特的引物RNA。IncB不相容性是由于具有相同结合特异性的复制起点之间对Rep蛋白的竞争所致。我们定位了与ColE2 - P9和ColE3 - CA38相关的15种ColE质粒(ColE2相关质粒)自主复制所需的区域,分析了它们的不相容性特性,并测定了9种代表性质粒复制子区域的核苷酸序列。结果表明,所有这些质粒在DNA复制起始及其控制方面具有共同机制。发现了5种IncA特异性类型、4种IncB特异性类型以及IncA和IncB类型的20种可能组合中的9种。Rep蛋白与复制起点相互作用的特异性可能由复制起点中特定位点的单核苷酸插入或缺失、几个核苷酸的替换以及Rep蛋白C末端特定区域明显相应的氨基酸序列插入或缺失和替换所决定。对于四种IncA特异性类型的质粒,反义RNA茎环结构环区的九核苷酸序列是相同的,这表明该序列具有进化意义。具有同源和非同源片段的复制子区域的镶嵌结构表明,其中一些是通过同源重组交换功能部分产生的。