Manickam Nandini, Joshi Kartikeya, Bhatt Monika J, Farabaugh Philip J
Department of Biological Sciences and Program in Molecular and Cell Biology, University of Maryland Baltimore County, 1000 Hilltop Circle, Baltimore, MD 21250, USA.
Department of Biological Sciences and Program in Molecular and Cell Biology, University of Maryland Baltimore County, 1000 Hilltop Circle, Baltimore, MD 21250, USA
Nucleic Acids Res. 2016 Feb 29;44(4):1871-81. doi: 10.1093/nar/gkv1506. Epub 2015 Dec 23.
Cellular health and growth requires protein synthesis to be both efficient to ensure sufficient production, and accurate to avoid producing defective or unstable proteins. The background of misreading error frequency by individual tRNAs is as low as 2 × 10(-6) per codon but is codon-specific with some error frequencies above 10(-3) per codon. Here we test the effect on error frequency of blocking post-transcriptional modifications of the anticodon loops of four tRNAs in Escherichia coli. We find two types of responses to removing modification. Blocking modification of tRNA(UUC)(Glu) and tRNA(QUC)(Asp) increases errors, suggesting that the modifications act at least in part to maintain accuracy. Blocking even identical modifications of tRNA(UUU)(Lys) and tRNA(QUA)(Tyr) has the opposite effect of decreasing errors. One explanation could be that the modifications play opposite roles in modulating misreading by the two classes of tRNAs. Given available evidence that modifications help preorder the anticodon to allow it to recognize the codons, however, the simpler explanation is that unmodified 'weak' tRNAs decode too inefficiently to compete against cognate tRNAs that normally decode target codons, which would reduce the frequency of misreading.
细胞的健康与生长要求蛋白质合成既要高效以确保足够的产量,又要准确以避免产生有缺陷或不稳定的蛋白质。单个转运RNA(tRNA)的错读错误频率背景低至每密码子2×10⁻⁶,但具有密码子特异性,有些错误频率高于每密码子10⁻³。在这里,我们测试了阻断大肠杆菌中四种tRNA反密码子环的转录后修饰对错误频率的影响。我们发现去除修饰有两种类型的反应。阻断tRNA(UUC)(Glu)和tRNA(QUC)(Asp)的修饰会增加错误,这表明这些修饰至少部分起到维持准确性的作用。阻断tRNA(UUU)(Lys)和tRNA(QUA)(Tyr)的相同修饰却有相反的效果,即减少错误。一种解释可能是这些修饰在调节两类tRNA的错读中发挥相反的作用。然而,鉴于现有证据表明修饰有助于使反密码子预先排列以使其能够识别密码子,更简单的解释是未修饰的“弱”tRNA解码效率太低,无法与正常解码靶密码子的同源tRNA竞争,这会降低错读频率。