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      Evolution of MHC class I genes in the European badger ( Meles meles)

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          Abstract

          The major histocompatibility complex (MHC) plays a central role in the adaptive immune system and provides a good model with which to understand the evolutionary processes underlying functional genes. Trans-species polymorphism and orthology are both commonly found in MHC genes; however, mammalian MHC class I genes tend to cluster by species. Concerted evolution has the potential to homogenize different loci, whereas birth-and-death evolution can lead to the loss of orthologs; both processes result in monophyletic groups within species. Studies investigating the evolution of MHC class I genes have been biased toward a few particular taxa and model species. We present the first study of MHC class I genes in a species from the superfamily Musteloidea. The European badger ( Meles meles) exhibits moderate variation in MHC class I sequences when compared to other carnivores. We identified seven putatively functional sequences and nine pseudogenes from genomic (gDNA) and complementary (cDNA) DNA, signifying at least two functional class I loci. We found evidence for separate evolutionary histories of the α1 and α2/α3 domains. In the α1 domain, several sequences from different species were more closely related to each other than to sequences from the same species, resembling orthology or trans-species polymorphism. Balancing selection and probable recombination maintain genetic diversity in the α1 domain, evidenced by the detection of positive selection and a recombination event. By comparison, two recombination breakpoints indicate that the α2/α3 domains have most likely undergone concerted evolution, where recombination has homogenized the α2/α3 domains between genes, leading to species-specific clusters of sequences. Our findings highlight the importance of analyzing MHC domains separately.

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          Codon-substitution models for heterogeneous selection pressure at amino acid sites.

          Comparison of relative fixation rates of synonymous (silent) and nonsynonymous (amino acid-altering) mutations provides a means for understanding the mechanisms of molecular sequence evolution. The nonsynonymous/synonymous rate ratio (omega = d(N)d(S)) is an important indicator of selective pressure at the protein level, with omega = 1 meaning neutral mutations, omega 1 diversifying positive selection. Amino acid sites in a protein are expected to be under different selective pressures and have different underlying omega ratios. We develop models that account for heterogeneous omega ratios among amino acid sites and apply them to phylogenetic analyses of protein-coding DNA sequences. These models are useful for testing for adaptive molecular evolution and identifying amino acid sites under diversifying selection. Ten data sets of genes from nuclear, mitochondrial, and viral genomes are analyzed to estimate the distributions of omega among sites. In all data sets analyzed, the selective pressure indicated by the omega ratio is found to be highly heterogeneous among sites. Previously unsuspected Darwinian selection is detected in several genes in which the average omega ratio across sites is 1. Genes undergoing positive selection include the beta-globin gene from vertebrates, mitochondrial protein-coding genes from hominoids, the hemagglutinin (HA) gene from human influenza virus A, and HIV-1 env, vif, and pol genes. Tests for the presence of positively selected sites and their subsequent identification appear quite robust to the specific distributional form assumed for omega and can be achieved using any of several models we implement. However, we encountered difficulties in estimating the precise distribution of omega among sites from real data sets.
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            Concerted and birth-and-death evolution of multigene families.

            Until around 1990, most multigene families were thought to be subject to concerted evolution, in which all member genes of a family evolve as a unit in concert. However, phylogenetic analysis of MHC and other immune system genes showed a quite different evolutionary pattern, and a new model called birth-and-death evolution was proposed. In this model, new genes are created by gene duplication and some duplicate genes stay in the genome for a long time, whereas others are inactivated or deleted from the genome. Later investigations have shown that most non-rRNA genes including highly conserved histone or ubiquitin genes are subject to this type of evolution. However, the controversy over the two models is still continuing because the distinction between the two models becomes difficult when sequence differences are small. Unlike concerted evolution, the model of birth-and-death evolution can give some insights into the origins of new genetic systems or new phenotypic characters.
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              Analyzing the mosaic structure of genes.

              Some genes in prokaryotes consist of a mosaic of regions derived from different ancestors by horizontal gene transfer. A method is described for demonstrating the statistical significance of such mosaic structure and for locating the crossover points separating different regions.
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                Author and article information

                Journal
                Ecol Evol
                Ecol Evol
                ece3
                Ecology and Evolution
                Blackwell Publishing Ltd (Oxford, UK )
                2045-7758
                2045-7758
                July 2012
                : 2
                : 7
                : 1644-1662
                Affiliations
                [1 ]Wildlife Conservation Research Unit, Department of Zoology, University of Oxford, Recanati-Kaplan Centre Tubney House, Abingdon Road, Tubney, Abingdon, Oxfordshire OX13 5QL, United Kingdom
                [2 ]NERC Biomolecular Analysis Facility, Department of Animal and Plant Sciences, University of Sheffield Western Bank, Sheffield, South Yorkshire, S10 2TN, United Kingdom
                [3 ]Behavioural Ecology and Self-Organization, University of Groningen P.O. Box 11103, 9700 CC Groningen, The Netherlands
                [4 ]Theoretical Biology, University of Groningen P.O. Box 11103, 9700 CC Groningen, The Netherlands
                Author notes
                Yung Wa Sin, Wildlife Conservation Research Unit, Department of Zoology, University of Oxford, Recanati-Kaplan Centre, Tubney House, Abingdon Road, Tubney, Abingdon, Oxfordshire, OX13 5QL, United Kingdom. Tel: +44 (0)1865 393 127; Fax: +44 (0)1865 393 101; E-mail: yungwa.sin@ 123456zoo.ox.ac.uk

                Funded by the Croucher Foundation (Hong Kong), Natural Environment Research Council (NERC) Biomolecular Analysis Facility and the Netherlands Organisation for Scientific Research.

                Article
                10.1002/ece3.285
                3434948
                22957169
                f4576b20-6dd6-45c6-8e69-7f09ad7698b7
                © 2012 The Authors. Published by Blackwell Publishing Ltd.

                Re-use of this article is permitted in accordance with the Creative Commons Deed, Attribution 2.5, which does not permit commercial exploitation.

                History
                : 25 April 2012
                : 27 April 2012
                Categories
                Original Research

                Evolutionary Biology
                trans-species polymorphism,birth-and-death evolution,concerted evolution,major histocompatibility complex,orthology,balancing selection

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