Young R A, Macklis R, Steitz J A
J Biol Chem. 1979 May 10;254(9):3264-71.
The transducing phages lambdadaroE and lambdadilv5, which carry the Escherichia coli ribosomal RNA operons rrnD and rrnX, respectively, have been mapped with the restriction endonucleases BamHI, EcoRI, HindIII, and Sma I. Using hybridization techniques, we have located the ribosomal RNA genes on these phage DNAs. The DNA sequence of the 437-base-pair 16 S-23 S ribosomal RNA intergenic spacer in the two rRNA operons rrnD and rrnX has been determined. The nucleotides examined exhibit only one base pair change between rrnD and rrnX. Both spacer regions contain the genes for tRNA1Ile and tRNA1BAla; the gene sequences are identical with the previously deduced tRNA sequences and are clustered within the first 60% of the spacer DNA. The most striking feature of the 16 S-23 S intergenic region in these two operons is the disparity in G-C content between the tRNA gene sequences (60% G-C) and the remaining spacer DNA (37% G-C). Spacer sequences are known to be involved in the processing of the ribosomal RNA transcript by RNase III and RNase P. In addition, we report the sequence of the first 108 base pairs of the 23 S rRNA gene.
转导噬菌体λdaroE和λdilv5分别携带大肠杆菌核糖体RNA操纵子rrnD和rrnX,已经用限制性内切酶BamHI、EcoRI、HindIII和Sma I进行了图谱绘制。利用杂交技术,我们已经在这些噬菌体DNA上定位了核糖体RNA基因。已经测定了rrnD和rrnX这两个rRNA操纵子中437个碱基对的16S - 23S核糖体RNA基因间隔区的DNA序列。所检测的核苷酸在rrnD和rrnX之间仅显示一个碱基对的变化。两个间隔区都包含tRNA1Ile和tRNA1BAla的基因;基因序列与先前推导的tRNA序列相同,并且聚集在间隔区DNA的前60%内。这两个操纵子中16S - 23S基因间隔区最显著的特征是tRNA基因序列(G - C含量为60%)和其余间隔区DNA(G - C含量为37%)之间G - C含量的差异。已知间隔区序列参与核糖核酸酶III和核糖核酸酶P对核糖体RNA转录本的加工。此外,我们报告了23S rRNA基因前108个碱基对的序列。