Reed R E, Baer M F, Guerrier-Takada C, Donis-Keller H, Altman S
Cell. 1982 Sep;30(2):627-36. doi: 10.1016/0092-8674(82)90259-8.
The gene encoding the RNA subunit (M1 RNA) of RNAase P (EC 3.1.26.5) from Escherichia coli has been isolated, and its complete nucleotide sequence, including flanking regions, has been determined. The promoter region, similar to others near genes under stringent control, and the site of transcription termination have been identified. The transcript from the gene (M1 RNA) can be drawn in a secondary structure that has approximately 60% G-C base pairs. One hairpin loop of this hypothetical structure has five contiguous nucleotides complementary to invariant nucleotides in the TpsiCG loop of all E. coli tRNAs. The M1 gene, when subcloned in the plasmid pBR325, can be amplified. It directs production of functional M1 RNA. In an E. coli strain thermosensitive for RNAase P function, the size of the gene transcript is the same as in wild-type E. coli, but less mature M1 RNA is made in the mutant cells.
编码来自大肠杆菌的核糖核酸酶P(EC 3.1.26.5)的RNA亚基(M1 RNA)的基因已被分离出来,并且已经确定了其完整的核苷酸序列,包括侧翼区域。已鉴定出与严格控制下的其他基因附近的启动子区域以及转录终止位点。该基因(M1 RNA)的转录本可以绘制出具有约60% G-C碱基对的二级结构。这种假设结构的一个发夹环有五个连续的核苷酸与所有大肠杆菌tRNA的TpsiCG环中的不变核苷酸互补。当M1基因亚克隆到质粒pBR325中时,可以进行扩增。它指导功能性M1 RNA的产生。在对核糖核酸酶P功能热敏的大肠杆菌菌株中,基因转录本的大小与野生型大肠杆菌中的相同,但突变细胞中产生的成熟M1 RNA较少。