Ogasawara N, Moriya S, Yoshikawa H
Nucleic Acids Res. 1983 Sep 24;11(18):6301-18. doi: 10.1093/nar/11.18.6301.
Structure and organization of two complete ribosomal RNA (rRNA) gene sets, rrnO and rrnA, were determined for the first time in Bacillus subtilis. They are located at the region of the replication origin of the chromosome. Each set constitutes a single operon of: two tandem promoters - leader sequence - 16S rRNA gene - Ile-tRNA gene - Ala-tRNA gene - 23S rRNA gene - 5S rRNA gene - termination signal. The first promoter (P1) of rrnO differs from that of rrnA in sequence and function. P1 of rrnO was used very little for transcription either in vivo or in vitro while P1 was predominantly used in rrnA. A putative transcript of the entire operon was determined and constructed into a secondary structure. Analysis of in vivo transcripts by S1 mapping revealed primary processing sites at the loop and stem structure of 16S rRNA in rrnO and rrnA. A unique sequence in the leader region of rrnO can be formed into a highly complexed secondary structure and affects processing of mature 16S rRNA. The sequences of the two spacer tRNA genes are highly conserved between B. subtilis and Escherichia coli.
首次在枯草芽孢杆菌中确定了两个完整核糖体RNA(rRNA)基因集rrnO和rrnA的结构与组织。它们位于染色体复制起点区域。每个基因集构成一个单一操纵子,包含:两个串联启动子 - 前导序列 - 16S rRNA基因 - 异亮氨酸 - tRNA基因 - 丙氨酸 - tRNA基因 - 23S rRNA基因 - 5S rRNA基因 - 终止信号。rrnO的第一个启动子(P1)在序列和功能上与rrnA的不同。rrnO的P1在体内或体外转录中很少被使用,而rrnA中P1主要被使用。确定了整个操纵子的推定转录本并构建成二级结构。通过S1图谱分析体内转录本揭示了rrnO和rrnA中16S rRNA的环和茎结构处的初级加工位点。rrnO前导区域中的独特序列可形成高度复杂的二级结构并影响成熟16S rRNA的加工。枯草芽孢杆菌和大肠杆菌之间两个间隔tRNA基因的序列高度保守。