Hartmann R K, Erdmann V A
Institut für Biochemie, Freie Universität Berlin, Federal Republic of Germany.
J Bacteriol. 1989 Jun;171(6):2933-41. doi: 10.1128/jb.171.6.2933-2941.1989.
A cloned 16S rRNA gene from the extreme thermophilic eubacterium Thermus thermophilus HB8 was used to characterize the in vivo expression of the 16S rRNA genes in this organism by nuclease S1 mapping. The gene represents an isolated transcription unit encoding solely 16S rRNA. Under exponential growth conditions, transcription was initiated at a single promoter, which represents the structural equivalent of Escherichia coli rrn P2 promoters. The promoter-leader region was very similar to the E. coli rrn P2 promoter-leader segment that is responsible for antitermination. The T. thermophilus leader region was approximately 85 nucleotides shorter than its E. coli P2 counterpart. Potential processing intermediates were correlated with a proposed secondary structure of T. thermophilus pre-16S rRNA.
从嗜热栖热菌HB8中克隆得到的16S rRNA基因,用于通过核酸酶S1图谱分析来表征该生物体中16S rRNA基因的体内表达情况。该基因代表一个仅编码16S rRNA的独立转录单元。在指数生长条件下,转录起始于单个启动子,该启动子与大肠杆菌rrn P2启动子结构等同。启动子-前导区与负责抗终止的大肠杆菌rrn P2启动子-前导区片段非常相似。嗜热栖热菌的前导区比其大肠杆菌P2对应区域短约85个核苷酸。潜在的加工中间体与嗜热栖热菌前体16S rRNA的二级结构模型相关。