Incorporation of transition to transversion ratio and nonsense mutations, improves the estimation of the number of synonymous and non-synonymous sites in codons

• Published in: DNA research Vol. 29; no. 4
• Main Authors: Aziz, Ruksana, Sen, Piyali, Beura, Pratyush Kumar, Das, Saurav, Tula, Debapriya, Dash, Madhusmita, Namsa, Nima Dondu, Deka, Ramesh Chandra, Feil, Edward J, Satapathy, Siddhartha Sankar, Ray, Suvendra Kumar
• Format: Journal Article
• Language: English
• Published: Oxford University Press 25-06-2022
• ISSN: 1340-2838; 1756-1663
• DOI: 10.1093/dnares/dsac023

A common approach to estimate the strength and direction of selection acting on protein coding sequences is to calculate the dN/dS ratio. The method to calculate dN/dS has been widely used by many researchers and many critical reviews have been made on its application after the proposition by Nei and Gojobori in 1986. However, the method is still evolving considering the non-uniform substitution rates and pretermination codons. In our study of SNPs in 586 genes across 156 Escherichia coli strains, synonymous polymorphism in 2-fold degenerate codons were higher in comparison to that in 4-fold degenerate codons, which could be attributed to the difference between transition (Ti) and transversion (Tv) substitution rates where the average rate of a transition is four times more than that of a transversion in general. We considered both the Ti/Tv ratio, and nonsense mutation in pretermination codons, to improve estimates of synonymous (S) and non-synonymous (NS) sites. The accuracy of estimating dN/dS has been improved by considering the Ti/Tv ratio and nonsense substitutions in pretermination codons. We showed that applying the modified approach based on Ti/Tv ratio and pretermination codons results in higher values of dN/dS in 29 common genes of equal reading-frames between E. coli and Salmonella enterica. This study emphasizes the robustness of amino acid composition with varying codon degeneracy, as well as the pretermination codons when calculating dN/dS values.