Persson B C, Jäger G, Gustafsson C
Department of Microbiology, Umeâ University, S-901 87 Umeâ, Sweden.
Nucleic Acids Res. 1997 Oct 15;25(20):4093-7. doi: 10.1093/nar/25.20.4093.
We have evidence that the open reading frame previously denoted spoU is necessary for tRNA (Gm18) 2'-O-methyltransferase activity. The spoU gene is located in the gmk-rpoZ-spoT-spoU-recG operon at 82 minutes on the Escherichia coli chromosome. The deduced amino acid sequence of spoU shows strong similarities to previously characterized 2'-O-methyltransferases. Comparison of the nucleoside modification pattern of hydrolyzed tRNA, 16S rRNA and 23S rRNA from wild-type and spoU null mutants showed that the modified nucleoside 2'-O-methylguanosine (Gm), present in a subset of E. coli tRNAs at residue 18, is completely absent in the spoU mutant, suggesting that spoU encodes tRNA (Gm18) 2'-O-methyltransferase. Nucleoside modification of 16S and 23S rRNA was unaffected in the spoU mutant. Insertions in the downstream recG gene did not affect RNA modification. Absence of Gm18 in tRNA does not influence growth rate under the tested conditions and does not interfere with activity of the SupF amber suppressor, a suppressor tRNA that normally has the Gm18 modification. We suggest that the spoU gene be renamed trmH (tRNA methylation).
我们有证据表明,先前命名为spoU的开放阅读框对于tRNA(Gm18)2'-O-甲基转移酶活性是必需的。spoU基因位于大肠杆菌染色体上82分钟处的gmk-rpoZ-spoT-spoU-recG操纵子中。spoU推导的氨基酸序列与先前表征的2'-O-甲基转移酶有很强的相似性。对野生型和spoU缺失突变体水解的tRNA、16S rRNA和23S rRNA的核苷修饰模式进行比较,结果表明,在大肠杆菌一部分tRNA的第18位存在的修饰核苷2'-O-甲基鸟苷(Gm)在spoU突变体中完全缺失,这表明spoU编码tRNA(Gm18)2'-O-甲基转移酶。spoU突变体中16S和23S rRNA的核苷修饰未受影响。下游recG基因中的插入不影响RNA修饰。tRNA中Gm18的缺失在测试条件下不影响生长速率,也不干扰SupF琥珀抑制子(一种通常具有Gm18修饰的抑制tRNA)的活性。我们建议将spoU基因重新命名为trmH(tRNA甲基化)。