Mankin A S, Kagramanova V K
Belozersky Laboratory of Molecular Biology and Bioorganic Chemistry, Moscow State University, USSR.
Nucleic Acids Res. 1988 May 25;16(10):4679-92. doi: 10.1093/nar/16.10.4679.
The transcription of the single ribosomal RNA gene cluster is initiated at an assemblage of promoters five of which were previously mapped in the 910 base pair region in front of the 16S rRNA gene. The nucleotide sequence between positions -1680 and -910 was determined and S1 nuclease mapping revealed therein two sites corresponding to the 5' ends of the primary transcripts. These two presumably represent the most distal promoters, P1 and P2, of the operon, P1 being separated from the 16S rRNA gene by more than 1250 bp. An additional putative "internal" promoter located within the operon body in the 16S/23S intergenic spacer was revealed by S1 nuclease mapping. A 528 bp long open reading frame is co-transcribed with the rRNA genes from the P1 promoter. Its possible functional implication is discussed.
单个核糖体RNA基因簇的转录起始于一组启动子,其中五个启动子先前已定位在16S rRNA基因前方910个碱基对的区域。确定了-1680至-910位之间的核苷酸序列,S1核酸酶图谱显示其中有两个与初级转录本5'端相对应的位点。这两个位点可能代表该操纵子最远端的启动子P1和P2,P1与16S rRNA基因的距离超过1250 bp。S1核酸酶图谱还揭示了位于操纵子体内16S/23S基因间隔区的一个额外的假定“内部”启动子。一个528 bp长的开放阅读框与来自P1启动子的rRNA基因共转录。文中讨论了其可能的功能意义。