Elseviers D, Petrullo L A, Gallagher P J
Nucleic Acids Res. 1984 Apr 25;12(8):3521-34. doi: 10.1093/nar/12.8.3521.
Novel E. coli mutants deficient in biosynthesis of 5- methylaminomethyl -2-thiouridine were isolated based on a phenotype of reduced readthrough at UAG codons. They define 2 new loci trmE and trmF , near 83' on the E. coli map. These mutants are different from strains carrying trmC mutations, which are known to confer a methylation deficiency in biosynthesis of 5- methylaminomethyl -2-thiouridine. tRNA from mutants carrying trmE or trmF mutations was shown to carry 2-thiouridine instead of 5- methylaminomethyl -2-thiouridine. This deficiency affects the triplet binding properties of the mutant tRNA. Our results suggest that the 5- methylaminomethyl group stabilizes the basepairing of this modified nucleotide with G, most likely through direct interaction with the ribosomal binding site(s).
基于UAG密码子通读减少的表型,分离出了缺乏5-甲基氨甲基-2-硫代尿苷生物合成能力的新型大肠杆菌突变体。它们在大肠杆菌图谱上靠近83'的位置定义了两个新基因座trmE和trmF。这些突变体与携带trmC突变的菌株不同,已知trmC突变会导致5-甲基氨甲基-2-硫代尿苷生物合成中的甲基化缺陷。携带trmE或trmF突变的突变体的tRNA显示携带2-硫代尿苷而非5-甲基氨甲基-2-硫代尿苷。这种缺陷影响了突变体tRNA的三联体结合特性。我们的结果表明,5-甲基氨甲基基团最有可能通过与核糖体结合位点的直接相互作用,稳定了这种修饰核苷酸与G的碱基配对。