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Optimization of the standard genetic code in terms of two mutation types: Point mutations and frameshifts

机译:在两个突变类型方面优化标准遗传密码:点突变和框架

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The distinct structure and universality of the standard genetic code (SGC) have fascinated the scientists ever since the first amino acid assignments were discovered. There are several hypotheses trying to explain the origin and evolution of this code. One of them postulates that the SGC evolved to minimize harmful effects of amino acid replacements in proteins, caused by mutations and translational errors. Many investigations concerning this hypothesis have already been carried out, but they were focused mainly on the consequences of single-point mutations. Therefore, we decided to check the influence of other types of mutations, i.e. insertions and deletions, on the robustness to amino acid replacements of the SGC. Such mutations cause shifts in the reading frame during the translation process which result in more harmful consequences in coded proteins than in the case of single-point mutations. We applied a multi-objective optimization algorithm to find the best and the worst genetic codes, regarding their robustness to both single-point and frameshift mutations, for various amino acid properties. Then we compared the features of the found codes with the properties of the standard genetic code. The results show that the SGC is not fully optimized for minimizing the effects of frameshift mutations but it is, nevertheless, much closer to the best solutions than to the worst ones. It implies that a certain tendency to minimize the costs of amino acids replacements resulting from various kinds of mutations is present in the standard genetic code.
机译:自标准遗传码(SGC)的不同结构和普遍性令人着迷于自第一个氨基酸分配以来的科学家。有几个假设试图解释这段代码的起源和演变。其中一个假设SGC演变以最小化由突变和平移误差引起的蛋白质中氨基酸置换的有害影响。许多关于这一假设的调查已经进行了,但它们主要集中在单点突变的后果。因此,我们决定检查其他类型突变的影响,即插入和缺失,对SGC的氨基酸替代的鲁棒性。这种突变在翻译过程中导致读取框架在编码蛋白中产生比单点突变的情况更有害的后果。我们应用了多目标优化算法,以寻找最佳和最差的遗传码,其对单点和帧突变突变的鲁棒性,各种氨基酸性能。然后,我们将发现代码的特征与标准遗传密码的属性进行了比较。结果表明,SGC没有完全优化,以最大限度地减少帧突变突变的影响,但它是比最糟糕的解决方案更接近最佳解决方案。它意味着在标准遗传密码中存在一定最小化各种突变产生的氨基酸替换成本的趋势。

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