Horie N, Yamaizumi Z, Kuchino Y, Takai K, Goldman E, Miyazawa T, Nishimura S, Yokoyama S
Department of Biophysics and Biochemistry, Graduate School of Science, University of Tokyo, Japan.
Biochemistry. 1999 Jan 5;38(1):207-17. doi: 10.1021/bi981865g.
Minor leucine tRNA species, tRNA(Leu)4 and tRNA(Leu)5, from Escherichia coli B have been reported to recognize leucine codons UUA and UUG [Goldman, E., Holmes, W. M., and Hatfield, G. W. (1979) J. Mol. Biol. 129, 567-585]. In the present study, these two tRNA(Leu) species were purified from E. coli A19, and the nucleotide sequences were determined by a post-labeling method. tRNA(Leu)5 was found to correspond to the tRNA gene reported as su degrees6 tRNA [Yoshimura, M., Inokuchi, H., and Ozeki, H. (1984) J. Mol. Biol. 177, 627-644]. The first letter of the anticodon was identified to be 2'-O-methylcytidine (Cm). tRNA(Leu)4 was identified as the minor leucine tRNA that has been sequenced previously (tRNA(Leu)UUR) [Yamaizumi, Z., Kuchino, Y., Harada, F., Nishimura, S., and McCloskey, J. A. (1980) J. Biol. Chem. 255, 2220-2225]. There was an unidentified modified nucleoside (N*) in the first position of the anticodon of tRNA(Leu)4. Nucleoside N* was isolated to homogeneity (1 A260 unit). By 1H NMR spectroscopy, nucleoside N was found to be a 2'-O-methyluridine derivative with a substituent having a -CH2NH2+CH2COO- moiety in position 5 of the uracil ring. On the basis of these NMR analyses together with mass spectrometry, the chemical structure of nucleoside N* was determined as 5-carboxymethylaminomethyl-2'-O-methyluridine (cmnm5Um). Nucleoside N* was thus found to be a novel type of naturally occurring modified uridine. Because of the conformational rigidity of Cm and cmnm5Um in the first position of the anticodon, these tRNA(Leu) species recognize the leucine codons UUA++ and UUG correctly, but never recognize the phenylalanine codons UUU and UUC.
据报道,来自大肠杆菌B的次要亮氨酸tRNA种类,即tRNA(Leu)4和tRNA(Leu)5,可识别亮氨酸密码子UUA和UUG [戈德曼,E.,霍姆斯,W. M.,和哈特菲尔德,G. W.(1979年)《分子生物学杂志》129卷,567 - 585页]。在本研究中,从大肠杆菌A19中纯化出这两种tRNA(Leu)种类,并通过后标记法测定了其核苷酸序列。发现tRNA(Leu)5与报道的作为su6 tRNA的tRNA基因相对应 [吉村,M.,井口,H.,和尾崎,H.(1984年)《分子生物学杂志》177卷,627 - 644页]。反密码子的第一个字母被鉴定为2'-O-甲基胞苷(Cm)。tRNA(Leu)4被鉴定为先前已测序的次要亮氨酸tRNA(tRNA(Leu)UUR)[山内,Z.,久智野,Y.,原田,F.,西村,S.,和麦克洛斯基,J. A.(1980年)《生物化学杂志》255卷,2220 - 2225页]。在tRNA(Leu)4反密码子的第一位存在一个未鉴定的修饰核苷(N*)。将核苷N分离至同质(1个A260单位)。通过1H核磁共振光谱分析,发现核苷N是一种2'-O-甲基尿苷衍生物,在尿嘧啶环的5位带有一个具有-CH2NH2+CH2COO-部分的取代基。基于这些核磁共振分析以及质谱分析,确定核苷N的化学结构为5-羧甲基氨基甲基-2'-O-甲基尿苷(cmnm5Um)。因此,核苷N*被发现是一种新型的天然存在的修饰尿苷。由于反密码子第一位的Cm和cmnm5Um的构象刚性,这些tRNA(Leu)种类能够正确识别亮氨酸密码子UUA和UUG,但从不识别苯丙氨酸密码子UUU和UUC。