Thomas Benjamin Thoha, Ogunkanmi Liasu Adebayo, Iwalokun Bamidele Abiodun, Popoola Omolara Dorcas
Department of Microbiology, Olabisi Onabanjo University, Ago Iwoye, Ogun State, Nigeria.
Department of Cell Biology and Genetics, University of Lagos, Akoka, Lagos, Nigeria.
Heliyon. 2019 Jun 15;5(6):e01881. doi: 10.1016/j.heliyon.2019.e01881. eCollection 2019 Jun.
This study determined the transition-transversion mutation in the gene of section in order to gain insight into the patterns of nucleotide base substitution and the process of molecular evolution using standard recommended techniques. Results obtained depict frequent occurrence of transition (23 ± 0.96) than transversion (11.37 ± 1.38) (p < 0.05) with C/T being the most frequently observed transitional base substitution and C/A the most frequently occurring transversional base change. The number of single base insertions (56 ± 1.00) were significantly higher than the observed single base deletions (38 ± 2.00) (p < 0.05) while varying degrees of two or more base deletions and insertions were also observed both inside and outside the open reading frame. The maximum likelihood value estimated for the gene was calculated to be -9458.80 in 423 positions of the final dataset while the transition-transversion ratio was estimated to be 0.50. The Tajima's neutrality test approaches seven (7) with the nucleotide diversity estimated to be approximately 65%. Evolutionary test depicts positive selection as ratio of non synonymous to synonymous divergence was found to be greater than ratio of the number of non synonymous to synonymous polymorphisms. The proportion of substitution driven by positive selection was calculated to be approximately 96.2%. This research therefore provides an insight into the understanding of gene mutation patterns as some of the observed indels resulted in frame shift mutations.
本研究确定了某节段基因中的转换-颠换突变,以便使用标准推荐技术深入了解核苷酸碱基替换模式和分子进化过程。获得的结果表明,转换(23±0.96)比颠换(11.37±1.38)更频繁发生(p<0.05),其中C/T是最常观察到的转换碱基替换,C/A是最常发生的颠换碱基变化。单碱基插入的数量(56±1.00)显著高于观察到的单碱基缺失数量(38±2.00)(p<0.05),同时在开放阅读框内外也观察到了不同程度的两个或更多碱基的缺失和插入。最终数据集中423个位置的该基因估计最大似然值计算为-9458.80,而转换-颠换比估计为0.50。 Tajima中性检验接近7,核苷酸多样性估计约为65%。进化检验显示为正选择,因为非同义与同义分歧的比率大于非同义与同义多态性数量的比率。由正选择驱动的替换比例计算约为96.2%。因此,本研究为理解基因突变模式提供了见解,因为一些观察到的插入缺失导致了移码突变。