Kowald A, Kirkwood T B
Laboratory of Mathematical Biology, National Institute for Medical Research, Mill Hill, London, U.K.
J Theor Biol. 1993 Feb 21;160(4):493-508. doi: 10.1006/jtbi.1993.1032.
Cellular homeostasis and the mechanisms which control homeostasis are important for understanding such fundamental processes as ageing and the origin of life. Several models have studied the importance of accurate protein synthesis for cellular stability, but these models have not considered the complexities of the translation process in any detail. Here we develop a new model which describes the interplay between aminoacyl-tRNA (aatRNA) synthetases, the cellular pool of charged tRNAs and the process of codon: anticodon recognition. We also take the processive character of the ribosomes into account. In common with previous work, our model predicts that the cellular translation apparatus can either be stable or deteriorate progressively with time. However, because our model explicitly describes different subreactions of the overall translation process, we are also able to assess the relative importance of accurate tRNA charging and codon: anticodon recognition for cellular stability. It appears that the tRNA charging by the aatRNA synthetases plays the key role in controlling the long-term stability of the cell. Ribosomal errors are less important because error-prone ribosomes, being processive, produce mainly inactive proteins which do not contribute to error propagation within the translation machinery.
细胞内稳态以及控制内稳态的机制对于理解诸如衰老和生命起源等基本过程至关重要。已有几种模型研究了精确蛋白质合成对细胞稳定性的重要性,但这些模型均未详细考虑翻译过程的复杂性。在此,我们开发了一种新模型,该模型描述了氨酰 - tRNA(aatRNA)合成酶、带电荷tRNA的细胞池以及密码子:反密码子识别过程之间的相互作用。我们还考虑了核糖体的持续性特征。与之前的工作一样,我们的模型预测细胞翻译装置可能随时间保持稳定,也可能逐渐恶化。然而,由于我们的模型明确描述了整个翻译过程的不同子反应,所以我们还能够评估精确的tRNA充电以及密码子:反密码子识别对细胞稳定性的相对重要性。看来,aatRNA合成酶对tRNA的充电在控制细胞的长期稳定性方面起着关键作用。核糖体错误的影响较小,因为易出错的持续性核糖体主要产生无活性的蛋白质,这些蛋白质不会在翻译机制内导致错误传播。