Log on / register
BioMed Central home | Journals A-Z | Feedback | Support | My details
Open AccessResearch

γ-MYN: a new algorithm for estimating Ka and Ks with consideration of variable substitution rates

Da-Peng Wang1,2* email, Hao-Lei Wan1,2* email, Song Zhang1,2,3* email and Jun Yu1,3 email

CAS Key Laboratory of Genome Sciences and Information, Beijing Institute of Genomics, Chinese Academy of Sciences, Beijing 100029, PR China

Graduate University of Chinese Academy of Sciences, Beijing 100039, PR China

Institute of Computing Technology, Chinese Academy of Sciences, Beijing 100080, PR China

author email corresponding author email* Contributed equally

Biology Direct 2009, 4:20doi:10.1186/1745-6150-4-20

Published: 16 June 2009

Abstract

Background

Over the past two decades, there have been several approximate methods that adopt different mutation models and used for estimating nonsynonymous and synonymous substitution rates (Ka and Ks) based on protein-coding sequences across species or even different evolutionary lineages. Among them, MYN method (a Modified version of Yang-Nielsen method) considers three major dynamic features of evolving DNA sequences–bias in transition/transversion rate, nucleotide frequency, and unequal transitional substitution but leaves out another important feature: unequal substitution rates among different sites or nucleotide positions.

Results

We incorporated a new feature for analyzing evolving DNA sequences–unequal substitution rates among different sites–into MYN method, and proposed a modified version, namely γ (gamma)-MYN, based on an assumption that the evolutionary rate at each site follows a mode of γ-distribution. We applied γ-MYN to analyze the key estimator of selective pressure ω (Ka/Ks) and other relevant parameters in comparison to two other related methods, YN and MYN, and found that neglecting the variation of substitution rates among different sites may lead to biased estimations of ω. Our new method appears to have minimal deviations when relevant parameters vary within normal ranges defined by empirical data.

Conclusion

Our results indicate that unequal substitution rates among different sites have variable influences on ω under different evolutionary rates while both transition/transversion rate ratio and unequal nucleotide frequencies affect Ka and Ks thus selective pressure ω.

Reviewers

This paper was reviewed by Kateryna Makova, David A. Liberles (nominated by David H Ardell), Zhaolei Zhang (nominated by Mark Gerstein), and Shamil Sunyaev.


© 1999-2010 BioMed Central Ltd unless otherwise stated. Part of Springer Science+Business Media.