Identification of physicochemical selective pressure on protein encoding nucleotide sequences
Sainudiin Raazesh, Wong Wendy SW, Nielsen Rasmus
BMC Bioinformatics · 2006
doi:10.1186/1471-2105-7-148 (opens in a new tab)
We email you when a new notice or a question about this paper appears.
Abstract
<p>Abstract</p> <p>Background</p> <p>Statistical methods for identifying positively selected sites in protein coding regions are one of the most commonly used tools in evolutionary bioinformatics. However, they have been limited by not taking the physiochemical properties of amino acids into account.</p> <p>Results</p> <p>We develop a new codon-based likelihood model for detecting site-specific selection pressures acting on specific physicochemical properties. Nonsynonymous substitutions are divided into substitutions that differ with respect to the physicochemical properties of interest, and those that do not. The substitution rates of these two types of changes, relative to the synonymous substitution rate, are then described by two parameters, <it>γ </it>and <it>ω </it>respectively. The new model allows us to perform likelihood ratio tests for positive selection acting on specific physicochemical properties of interest.</p> <p>The new method is first used to analyze simulated data and is shown to have good power and accuracy in detecting physicochemical selective pressure. We then re-analyze data from the class-I alleles of the human Major Histocompatibility Complex (MHC) and from the abalone sperm lysine.</p> <p>Conclusion</p> <p>Our new method allows a more flexible framework to identify selection pressure on particular physicochemical properties.</p>
Abstract licence: CC BY-NC-ND
Reads
Read by people on this page
None yet.
Checked or read by AI through naulon
None yet.
A person counts once a day per paper. We keep no cookie and no address: a reader is a hash that changes every day. Any month under five reads shows no number.
Are you an author?
Is this your paper?
Claim it to add your note and be paid when agents cite it. Free.