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遗传密码子中单个核苷酸取代的分析——概率与结果

An Analysis of Single Nucleotide Substitution in Genetic Codons - Probabilities and Outcomes.

作者信息

Abdullah Tariq, Faiza Muniba, Pant Prashant, Rayyan Akhtar Mohd, Pant Pratibha

机构信息

Department of Computer Science, Faculty of Natural Sciences, Jamia Millia Islamia, New Delhi , India.

Department of Botany,Dyal Singh College, University of Delhi, New Delhi - 110003, India.

出版信息

Bioinformation. 2016 Jun 15;12(3):98-104. doi: 10.6026/97320630012098. eCollection 2016.

Abstract

BACKGROUND

Single nucleotide substitutions (SNS) in genetic codon are of prime importance due to their ability to alter an amino acid sequence as a result. Given the nature of genetic code, any SNS is expected to change the protein sequence randomly into any of the 64 possible codons. In this paper, we present a theoretical analysis of how single nucleotide substitutions in genetic codon may affect resulting amino acid residue and what is the most likely amino acid that will get selected as a result.

METHODS

A probability matrix was developed showing possible changes and routes likely being followed as a result of base substitution mutation causing changes at the translational level for the amino acid being encoded.

RESULTS

We observe that in event of single base pair substitution in a given amino acid; a chosen set of amino acids is theoretically more probable to be resulted suggesting a directional rather than a random change. This study also indicates that for a given amino acid coded by a number of synonymous codons, all synonymous codons will result into same list of amino acids in case of all possible SNS at three positions.

CONCLUSION

The present work has resulted into development of a theoretical probability matrix which can be used to predict changes in amino acid residues in a protein sequence caused by single base substitutions.

摘要

背景

遗传密码子中的单核苷酸替换(SNS)至关重要,因为其能够改变氨基酸序列。鉴于遗传密码的性质,任何单核苷酸替换都可能将蛋白质序列随机改变为64种可能密码子中的任何一种。在本文中,我们对遗传密码子中的单核苷酸替换如何影响所得氨基酸残基以及最有可能被选择的氨基酸进行了理论分析。

方法

构建了一个概率矩阵,展示了由于碱基替换突变导致编码氨基酸在翻译水平发生变化时可能的变化情况及可能遵循的途径。

结果

我们观察到,在给定氨基酸发生单碱基对替换的情况下,理论上一组特定的氨基酸更有可能出现,这表明变化是有方向的而非随机的。本研究还表明,对于由多个同义密码子编码的给定氨基酸,在三个位置发生所有可能的单核苷酸替换时,所有同义密码子都会产生相同的氨基酸列表。

结论

目前的工作已形成一个理论概率矩阵,可用于预测单碱基替换引起的蛋白质序列中氨基酸残基的变化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8fc0/5267951/f9f175c85f6b/97320630012098F1.jpg

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