FAS Center for Systems Biology, Department of Molecular and Cellular Biology, and School of Engineering and Applied Sciences, Harvard University, Cambridge, MA 02138, USA.
Proc Natl Acad Sci U S A. 2013 Feb 5;110(6):2419-24. doi: 10.1073/pnas.1211077110. Epub 2012 Dec 31.
The genetic code underlying protein synthesis is a canonical example of a degenerate biological system. Degeneracies in physical and biological systems can be lifted by external perturbations, thus allowing degenerate systems to exhibit a wide range of behaviors. Here we show that the degeneracy of the genetic code is lifted by environmental perturbations to regulate protein levels in living cells. By measuring protein synthesis rates from a synthetic reporter library in Escherichia coli, we find that environmental perturbations, such as reduction of cognate amino acid supply, lift the degeneracy of the genetic code by splitting codon families into a hierarchy of robust and sensitive synonymous codons. Rates of protein synthesis associated with robust codons are up to 100-fold higher than those associated with sensitive codons under these conditions. We find that the observed hierarchy between synonymous codons is not determined by usual rules associated with tRNA abundance and codon usage. Rather, competition among tRNA isoacceptors for aminoacylation underlies the robustness of protein synthesis. Remarkably, the hierarchy established using the synthetic library also explains the measured robustness of synthesis for endogenous proteins in E. coli. We further found that the same hierarchy is reflected in the fitness cost of synonymous mutations in amino acid biosynthesis genes and in the transcriptional control of σ-factor genes. Our study suggests that organisms can exploit degeneracy lifting as a general strategy to adapt protein synthesis to their environment.
蛋白质合成所依赖的遗传密码是退化生物系统的典型例子。物理和生物系统中的简并性可以通过外部干扰来消除,从而使退化系统表现出广泛的行为。在这里,我们表明,环境干扰可以消除遗传密码的简并性,从而调节活细胞中的蛋白质水平。通过测量大肠杆菌中合成报告基因文库的蛋白质合成速率,我们发现环境干扰,如减少对应氨基酸的供应,通过将密码子家族划分为稳健和敏感同义密码子的层次结构,消除遗传密码的简并性。在这些条件下,与稳健密码子相关的蛋白质合成速率比与敏感密码子相关的蛋白质合成速率高 100 倍。我们发现,观察到的同义密码子之间的层次结构不是由与 tRNA 丰度和密码子使用相关的常用规则决定的。相反,在氨酰化过程中 tRNA 同工受体之间的竞争是蛋白质合成稳健性的基础。值得注意的是,使用合成文库建立的层次结构也解释了大肠杆菌中内源性蛋白质测量的合成稳健性。我们进一步发现,相同的层次结构反映在氨基酸生物合成基因中同义突变的适应成本和σ因子基因的转录控制中。我们的研究表明,生物体可以利用简并性消除作为一种将蛋白质合成适应环境的一般策略。