2005
DOI: 10.1093/molbev/msi096
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Rapid Evolution of the MH Class I Locus Results in Different Allelic Compositions in Recently Diverged Populations of Atlantic Salmon

Abstract: We compared major histocompatibility class I allelic diversity in two currently reproductively isolated Atlantic salmon (Salmo salar) populations (Irish and Norwegian) with a common postglacial origin in order to test for among-population differences in allelic composition and patterns of recombination and point mutation. We also examined the evidence for adaptive molecular divergence at this locus by analyzing the rate of amino acid replacement in relation to a neutral expectation. Contrary to our prediction,… Show more

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Cited by 57 publications
(41 citation statements)
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“…As a ubiquitous evolutionary force, recombination has been shown to contribute substantially to MHC diversity, creating new alleles in isolated populations (Consuegra et al, 2005). However, in the present study, we have not detected signal of recombination in the MHC-I exon 4 sequences.…”
Section: Effects Of Recombination and Purifying Selectioncontrasting
confidence: 82%
“…As a ubiquitous evolutionary force, recombination has been shown to contribute substantially to MHC diversity, creating new alleles in isolated populations (Consuegra et al, 2005). However, in the present study, we have not detected signal of recombination in the MHC-I exon 4 sequences.…”
Section: Effects Of Recombination and Purifying Selectioncontrasting
confidence: 82%
“…Kundu and Faulkes (2004) were able to identify PSS in four species of African mole-rats (Bathyergidae: Heliophobius argenteocinereus, Heterocephalus glaber, Cryptomys hottentotus hottentotus, Cryptomys damarensis). As in our study in Malagasy fattailed dwarf lemurs, the comparisons of PSS in Atlantic salmon (Salmo salar) (Consuegra et al, 2005) and in two chamois subspecies (Rupicapra spp.) revealed high but not complete coincidence with the human ABS.…”
Section: Discussionmentioning
confidence: 65%
“…Therefore, simulations were initiated with a single allele and new alleles were introduced at one of two per-locus rates (m L ¼ 2m, where m is the per-gene mutation rate): 10 À5 and 10 À6 . Here we consider these allele-introduction rates to represent the combined effects of point mutation and recombination, both of which are important to the generation of MHC diversity (Martinsohn et al 1999;Ohta 1999;Richman et al 2003;Consuegra et al 2005;Reusch and Langefors 2005;Schaschl et al 2006). We ran simulations with three different effective population sizes (N e ) of 10 3 , 10 4 , and 10…”
mentioning
confidence: 99%