Moriya J, Yokogawa T, Wakita K, Ueda T, Nishikawa K, Crain P F, Hashizume T, Pomerantz S C, McCloskey J A, Kawai G
Department of Industrial Chemistry, Faculty of Engineering, University of Tokyo, Japan.
Biochemistry. 1994 Mar 1;33(8):2234-9. doi: 10.1021/bi00174a033.
Methionine tRNA was purified from bovine liver mitochondria, and its nucleotide sequence was determined. The tRNA possesses only three posttranscriptionally modified nucleosides, two pseudouridines in the anticodon and T stems and a previously unknown nucleoside specified by the gene sequence as cytidine, in the first position of the anticodon. Structure analysis of the anticodon nucleoside by mass spectrometry revealed a molecular mass 28 Da greater than that of cytidine, and unmodified ribose, with substitution at C-5 implied by hydrogen-deuterium exchange experiments. Proton NMR of the intact tRNA showed presence of a formyl moiety, thus leading to the candidate structure 5-formylcytidine (f5C), not a previously known compound. The structure assignment was confirmed by chemical synthesis and comparison of data from combined HPLC/mass spectrometry and proton NMR for the natural and synthetic nucleosides. The potential function of f5C in the tRNA(Met) anticodon is discussed with regard to codon-anticodon interactions.
从牛肝线粒体中纯化出甲硫氨酸转运核糖核酸(tRNA),并测定了其核苷酸序列。该tRNA仅含有三种转录后修饰核苷:反密码子和T茎中的两个假尿苷,以及基因序列指定为胞苷的一个位于反密码子第一位的此前未知核苷。通过质谱对反密码子核苷进行结构分析,结果显示其分子量比胞苷大28道尔顿,且核糖未修饰,氢氘交换实验表明C-5位有取代。完整tRNA的质子核磁共振显示存在甲酰基部分,从而得出候选结构5-甲酰基胞苷(f5C),这并非一种已知化合物。通过化学合成以及对天然和合成核苷的高效液相色谱/质谱联用数据与质子核磁共振数据进行比较,证实了结构归属。关于密码子与反密码子相互作用,讨论了f5C在tRNA(Met)反密码子中的潜在功能。