Prediction of the effects of the top 10 synonymous mutations from 26645 SARS-CoV-2 genomes of early pandemic phase.

Q2 Pharmacology, Toxicology and Pharmaceutics F1000Research Pub Date : 2024-09-18 eCollection Date: 2021-01-01 DOI:10.12688/f1000research.72896.3
Wan Xin Boon, Boon Zhan Sia, Chong Han Ng
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Abstract

Background: The emergence of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) had led to a global pandemic since December 2019. SARS-CoV-2 is a single-stranded RNA virus, which mutates at a higher rate. Multiple works had been done to study nonsynonymous mutations, which change protein sequences. However, there is little study on the effects of SARS-CoV-2 synonymous mutations, which may affect viral fitness. This study aims to predict the effect of synonymous mutations on the SARS-CoV-2 genome.

Methods: A total of 26645 SARS-CoV-2 genomic sequences retrieved from Global Initiative on Sharing all Influenza Data (GISAID) database were aligned using MAFFT. Then, the mutations and their respective frequency were identified. Multiple RNA secondary structures prediction tools, namely RNAfold, IPknot++ and MXfold2 were applied to predict the effect of the mutations on RNA secondary structure and their base pair probabilities was estimated using MutaRNA. Relative synonymous codon usage (RSCU) analysis was also performed to measure the codon usage bias (CUB) of SARS-CoV-2.

Results: A total of 150 synonymous mutations were identified. The synonymous mutation identified with the highest frequency is C3037U mutation in the nsp3 of ORF1a. Of these top 10 highest frequency synonymous mutations, C913U, C3037U, U16176C and C18877U mutants show pronounced changes between wild type and mutant in all 3 RNA secondary structure prediction tools, suggesting these mutations may have some biological impact on viral fitness. These four mutations show changes in base pair probabilities. All mutations except U16176C change the codon to a more preferred codon, which may result in higher translation efficiency.

Conclusion: Synonymous mutations in SARS-CoV-2 genome may affect RNA secondary structure, changing base pair probabilities and possibly resulting in a higher translation rate. However, lab experiments are required to validate the results obtained from prediction analysis.

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预测 26645 个 SARS-CoV-2 早期流行期基因组中前 10 个同义突变的影响。
背景:自 2019 年 12 月以来,严重急性呼吸系统综合征冠状病毒 2(SARS-CoV-2)的出现导致了全球大流行。SARS-CoV-2 是一种单链 RNA 病毒,变异率较高。已有多项研究对改变蛋白质序列的非同义突变进行了研究。然而,关于 SARS-CoV-2 同义突变的影响却鲜有研究,而这种突变可能会影响病毒的适应性。本研究旨在预测同义突变对 SARS-CoV-2 基因组的影响:方法:使用 MAFFT 对从全球流感数据共享倡议(GISAID)数据库中检索到的 26645 个 SARS-CoV-2 基因组序列进行比对。然后,确定了突变及其各自的频率。应用多种 RNA 二级结构预测工具,即 RNAfold、IPknot++ 和 MXfold2,预测突变对 RNA 二级结构的影响,并使用 MutaRNA 估算其碱基对概率。还进行了相对同义密码子使用(RSCU)分析,以测量 SARS-CoV-2 的密码子使用偏差(CUB):结果:共鉴定出 150 个同义突变。结果:共发现 150 个同义突变,频率最高的同义突变是 ORF1a 的 nsp3 中的 C3037U 突变。在这10个频率最高的同义突变中,C913U、C3037U、U16176C和C18877U突变体在所有3种RNA二级结构预测工具中都显示出野生型和突变体之间的明显变化,表明这些突变可能对病毒的适应性有一定的生物学影响。这四个突变显示了碱基对概率的变化。除 U16176C 外,所有突变都将密码子变为更优选的密码子,这可能会提高翻译效率:结论:SARS-CoV-2 基因组中的同义突变可能会影响 RNA 二级结构,改变碱基配对概率,从而可能提高翻译率。然而,要验证预测分析得出的结果,还需要实验室实验。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
F1000Research
F1000Research Pharmacology, Toxicology and Pharmaceutics-Pharmacology, Toxicology and Pharmaceutics (all)
CiteScore
5.00
自引率
0.00%
发文量
1646
审稿时长
1 weeks
期刊介绍: F1000Research publishes articles and other research outputs reporting basic scientific, scholarly, translational and clinical research across the physical and life sciences, engineering, medicine, social sciences and humanities. F1000Research is a scholarly publication platform set up for the scientific, scholarly and medical research community; each article has at least one author who is a qualified researcher, scholar or clinician actively working in their speciality and who has made a key contribution to the article. Articles must be original (not duplications). All research is suitable irrespective of the perceived level of interest or novelty; we welcome confirmatory and negative results, as well as null studies. F1000Research publishes different type of research, including clinical trials, systematic reviews, software tools, method articles, and many others. Reviews and Opinion articles providing a balanced and comprehensive overview of the latest discoveries in a particular field, or presenting a personal perspective on recent developments, are also welcome. See the full list of article types we accept for more information.
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