Anderson W F
Proc Natl Acad Sci U S A. 1969 Feb;62(2):566-73. doi: 10.1073/pnas.62.2.566.
Two in vitro protein-synthesizing systems derived from E. coli have been utilized to demonstrate that the concentration of a tRNA species can regulate the rate of translation of a messenger RNA. (a) The rate of poly-U-directed C(14)-phenylalanine incorporation into protein is stimulated by concentrations of tRNA(Phe) from 1.5 x 10(-8) M to 3.0 x 10(-6) M, the latter representing a tRNA(Phe)/70S ribosome ratio of 7. (b) The rate of translation of poly A,G in a S-30 protein-synthesizing system derived from E. coli is limited by the amount of tRNA(Arg) recognizing the codewords AGA and AGG present in the extract. Polypeptide synthesis can be stimulated in direct proportion to the amount of this tRNA(Arg) species added to the reaction mixture. A mechanism for regulating the rate of protein synthesis at the translational level may be the slowing of polypeptide chain propagation at certain codons due to the presence of rate-limiting tRNA species.
来自大肠杆菌的两种体外蛋白质合成系统已被用于证明一种tRNA种类的浓度可以调节信使RNA的翻译速率。(a) 从1.5×10(-8) M到3.0×10(-6) M的tRNA(Phe)浓度刺激了聚-U指导的C(14)-苯丙氨酸掺入蛋白质的速率,后者代表tRNA(Phe)/70S核糖体的比例为7。(b) 在源自大肠杆菌的S-30蛋白质合成系统中,聚A,G的翻译速率受到识别提取物中存在的密码子AGA和AGG的tRNA(Arg)量的限制。多肽合成可以与添加到反应混合物中的这种tRNA(Arg)种类的量成正比地受到刺激。在翻译水平上调节蛋白质合成速率的一种机制可能是由于存在限速tRNA种类,多肽链在某些密码子处的延伸减慢。