Jemiolo D K, Taurence J S, Giese S
Biology Department, Vassar College, Poughkeepsie, NY 12601.
Nucleic Acids Res. 1991 Aug 11;19(15):4259-65. doi: 10.1093/nar/19.15.4259.
Mutations were constructed at three sites in 16S rRNA in E. coli by oligonucleotide-directed mutagenesis, and cloned into the rrnB operon on either pKK3535 or pNO2680. The mutated bases, G966, C967, and G1207, are located in the 3' major domain of 16S rRNA and are sites post-transcriptionally modified by methylation. We constructed a deletion mutation at C967 (delta 967) and three substitution mutations at each of the following sites: G966, C967, and G1207. By maxicell analysis, we found that all of the mutations were processed normally and incorporated into 30S subunits and 70S ribosomes. We found that delta 967 was a dominant lethal mutation while the substitution mutations at G966 and C967 had no effects on cell growth rate. The mutants C1207 and U1207 were shown to have dominant lethal phenotypes while A1207 had no effect on cell growth rate. These results help to establish the importance of methyl-modified regions to ribosome function.
通过寡核苷酸定向诱变在大肠杆菌16S rRNA的三个位点构建突变,并克隆到pKK3535或pNO2680上的rrnB操纵子中。突变碱基G966、C967和G1207位于16S rRNA的3'主要结构域,是转录后发生甲基化修饰的位点。我们在C967处构建了缺失突变(δ967),并在以下每个位点构建了三个替代突变:G966、C967和G1207。通过大细胞分析,我们发现所有突变均正常加工并整合到30S亚基和70S核糖体中。我们发现δ967是显性致死突变,而G966和C967处的替代突变对细胞生长速率没有影响。突变体C1207和U1207表现出显性致死表型,而A1207对细胞生长速率没有影响。这些结果有助于确定甲基修饰区域对核糖体功能的重要性。