Shimizu M, Asahara H, Tamura K, Hasegawa T, Himeno H
Institute of Space and Astronautical Science, Kanagawa Pref., Japan.
J Mol Evol. 1992 Nov;35(5):436-43. doi: 10.1007/BF00171822.
The T7 polymerase transcription system was used for in vitro synthesis of unmodified versions of the E. coli tRNA mutants that insert asparagine, cysteine, glycine, histidine, and serine. These tRNAs were used to qualitatively explore the role of some anticodon bases and the discriminator nucleotide in the recognition of tRNA by aminoacyl-tRNA synthetases. Coupled with data from earlier studies, these new results essentially complete a survey of all E. coli tRNAs with respect to the involvement of anticodon bases and the discriminator nucleotide in tRNA recognition. It is found that in the vast majority of tRNAs both of these elements are significant components of tRNA identity. This is not universally true, however. Anticodon sequences are unimportant in tRNA(Ser), tRNA(Leu), and tRNA(Ala) while the discriminator base is inconsequential in tRNA(Ser) and tRNA(Thr). The significance of these results for origin-of-life studies is discussed.
T7聚合酶转录系统用于体外合成插入天冬酰胺、半胱氨酸、甘氨酸、组氨酸和丝氨酸的未修饰版本的大肠杆菌tRNA突变体。这些tRNA用于定性探索一些反密码子碱基和鉴别核苷酸在氨酰-tRNA合成酶识别tRNA中的作用。结合早期研究的数据,这些新结果基本完成了对所有大肠杆菌tRNA中反密码子碱基和鉴别核苷酸参与tRNA识别的调查。研究发现,在绝大多数tRNA中,这两个元件都是tRNA身份的重要组成部分。然而,情况并非普遍如此。反密码子序列在tRNA(Ser)、tRNA(Leu)和tRNA(Ala)中并不重要,而鉴别碱基在tRNA(Ser)和tRNA(Thr)中无关紧要。讨论了这些结果对生命起源研究的意义。