Nielsen A K, Douthwaite S, Vester B
Department of Molecular Biology, University of Odense, Denmark.
RNA. 1999 Aug;5(8):1034-41. doi: 10.1017/s1355838299990349.
Erm methyltransferases modify bacterial 23S ribosomal RNA at adenosine 2058 (A2058, Escherichia coli numbering) conferring resistance to macrolide, lincosamide, and streptogramin B (MLS) antibiotics. The motif that is recognized by Erm methyltransferases is contained within helix 73 of 23S rRNA and the adjacent single-stranded region around A2058. An RNA transcript of 72 nt that displays this motif functions as an efficient substrate for the ErmE methyltransferase. Pools of degenerate RNAs were formed by doping 34-nt positions that extend over and beyond the putative Erm recognition motif within the 72-mer RNA. The RNAs were passed through a series of rounds of methylation with ErmE. After each round, RNAs were selected that had partially or completely lost their ability to be methylated. After several rounds of methylation/selection, 187 subclones were analyzed. Forty-three of the subclones contained substitutions at single sites, and these are confined to 12 nucleotide positions. These nucleotides, corresponding to A2051-A2060, C2611, and A2614 in 23S rRNA, presumably comprise the RNA recognition motif for ErmE methyltransferase. The structure formed by these nucleotides is highly conserved throughout bacterial rRNAs, and is proposed to constitute the motif that is recognized by all the Erm methyltransferases.
Erm甲基转移酶在腺苷2058(A2058,大肠杆菌编号)处修饰细菌23S核糖体RNA,赋予对大环内酯类、林可酰胺类和链阳菌素B(MLS)抗生素的抗性。Erm甲基转移酶识别的基序包含在23S rRNA的螺旋73以及A2058周围的相邻单链区域内。一个显示该基序的72个核苷酸的RNA转录本可作为ErmE甲基转移酶的有效底物。通过在72聚体RNA中对延伸到假定的Erm识别基序及其以外的34个核苷酸位置进行掺杂,形成了简并RNA池。这些RNA经过一系列用ErmE进行甲基化的轮次。每一轮之后,选择那些部分或完全失去甲基化能力的RNA。经过几轮甲基化/选择后,对187个亚克隆进行了分析。其中43个亚克隆在单个位点含有取代,且这些取代局限于12个核苷酸位置。这些核苷酸对应于23S rRNA中的A2051 - A2060、C2611和A2614,推测构成了ErmE甲基转移酶的RNA识别基序。这些核苷酸形成的结构在整个细菌rRNA中高度保守,并被认为构成了所有Erm甲基转移酶识别的基序。