Venkova-Canova Tatiana, Pátek Miroslav, Nesvera Jan
Institute of Microbiology, Academy of Sciences of the Czech Republic, CZ-14220 Prague 4, Czech Republic.
J Bacteriol. 2003 Apr;185(8):2402-9. doi: 10.1128/JB.185.8.2402-2409.2003.
The cryptic multicopy plasmid pGA1 (4,826 bp) from Corynebacterium glutamicum LP-6 belongs to the fifth group of rolling-circle-replicating plasmids. A determinant, which negatively controls pGA1 replication, was localized in the leader region of the rep gene coding for the initiator of plasmid replication. This region, when cloned into the compatible vector pEC6, was found to cause decrease of segregational stability of the pGA1 derivative pKG48. A promoter and a single transcriptional start site were found in the rep leader region in orientation opposite to the rep gene. These results suggest that a small countertranscribed RNA (ctRNA) (ca. 89 nucleotides in length), which might inhibit translation of pGA1 rep gene, is formed. Analysis of predicted secondary structure of the pGA1-encoded ctRNA revealed features common with the known ctRNAs in bacteria. Inactivation of the promoter P-ctRNA caused a dramatic increase of copies of the respective plasmid, which proved a negative role of the ctRNA in control of pGA1 copy number. A region between the promoters Prep and P-ctRNA with a potential to form secondary structures on both ctRNA and rep mRNA was found to cause low activity of the rep promoter even when promoter P-ctRNA was deleted. Thus, the sequence within the rep leader region itself seems to act, in addition to the ctRNA, as a second regulatory element of a novel type, negatively influencing expression of the pGA1 rep gene.
来自谷氨酸棒杆菌LP-6的隐蔽多拷贝质粒pGA1(4826 bp)属于滚环复制质粒的第五组。一个对pGA1复制起负调控作用的决定簇定位于编码质粒复制起始蛋白的rep基因的前导区。当将该区域克隆到相容载体pEC6中时,发现它会导致pGA1衍生物pKG48的分离稳定性降低。在rep基因的前导区发现了一个启动子和一个单一转录起始位点,其方向与rep基因相反。这些结果表明,可能形成了一种小的反式转录RNA(ctRNA)(长度约89个核苷酸),它可能抑制pGA1 rep基因的翻译。对pGA1编码的ctRNA预测二级结构的分析揭示了与细菌中已知ctRNA共有的特征。ctRNA启动子P-ctRNA的失活导致相应质粒拷贝数急剧增加,这证明了ctRNA在控制pGA1拷贝数方面的负作用。即使删除了启动子P-ctRNA,在启动子Prep和P-ctRNA之间的一个区域,在ctRNA和rep mRNA上都有形成二级结构的潜力,被发现会导致rep启动子活性降低。因此,rep基因前导区内的序列本身似乎除了ctRNA之外,还作为一种新型的第二调控元件,对pGA1 rep基因的表达产生负影响。