Gavini N, Pulakat L
Department of Molecular Biology and Biochemistry, School of Biological Sciences, University of California, Irvine 92717.
J Biol Chem. 1992 Feb 5;267(4):2240-3.
The redundant genetic codons NNU and NNC (where N is A, T, G, or C) specify the same amino acid and are decoded by their cognate tRNAs, which contain either a guanosine or a modified base in the wobble position of the anticodons. Since tRNAs with an adenosine in the wobble position of the anticodon, which are complementary to the NNU codons, are not found naturally, we have generated a tRNA(Phe) with AAA anticodon and examined how an adenosine in the wobble position would affect its biological function in Escherichia coli. We found that the tRNA(Phe) with GAA anticodon (wild-type) repressed the expression of the pheA gene via tRNA(Phe)-mediated attenuation of transcription, whereas the tRNA(Phe) with AAA anticodon did not influence the expression of the pheA gene. Furthermore, elevated levels of tRNA(Phe)(AAA) did not support the growth of an E. coli strain carrying a temperature-sensitive mutation in the pheS gene at 42 degrees C. Since the presence of a multicopy plasmid carrying the gene that encodes tRNA(Phe)(GAA), a substrate for phenylalanyl tRNA synthetase, enables the E. coli strain carrying the pheS(Ts) mutation to grow at 42 degrees C, the above observation suggests that unlike tRNA(Phe)(GAA), tRNA(Phe)(AAA) is not a good substrate for phenylalanyl-tRNA synthetase. Therefore, we postulate that the presence of adenosine at the wobble position of anticodons was specifically eliminated and the tRNAs with guanosine or a modified base in the wobble position were selected to decode both NNU and NNC codons in E. coli.
冗余遗传密码子NNU和NNC(其中N为A、T、G或C)编码相同的氨基酸,并由其同源tRNA解码,这些tRNA在反密码子的摆动位置含有鸟苷或修饰碱基。由于在自然界中未发现反密码子摆动位置带有腺苷且与NNU密码子互补的tRNA,我们构建了一种带有AAA反密码子的tRNA(Phe),并研究了反密码子摆动位置的腺苷如何影响其在大肠杆菌中的生物学功能。我们发现,带有GAA反密码子(野生型)的tRNA(Phe)通过tRNA(Phe)介导的转录衰减抑制pheA基因的表达,而带有AAA反密码子的tRNA(Phe)不影响pheA基因的表达。此外,tRNA(Phe)(AAA)水平升高并不能支持在pheS基因中携带温度敏感突变的大肠杆菌菌株在42℃下生长。由于携带编码tRNA(Phe)(GAA)(苯丙氨酰tRNA合成酶的底物)基因的多拷贝质粒的存在,使携带pheS(Ts)突变的大肠杆菌菌株能够在42℃下生长,上述观察结果表明,与tRNA(Phe)(GAA)不同,tRNA(Phe)(AAA)不是苯丙氨酰-tRNA合成酶的良好底物。因此,我们推测,在大肠杆菌中,反密码子摆动位置的腺苷被特异性去除,而选择了摆动位置带有鸟苷或修饰碱基的tRNA来解码NNU和NNC密码子。