MBE Advance Access published online on February 2, 2005
Molecular Biology and Evolution, doi:10.1093/molbev/msi096
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
1 Institute of Zoology, Zoological Society of London, Regent's Park, London NW1 4RY, U.K.
* To whom correspondence should be addressed. We compared major histocompatibility (MH) class I allelic diversity in two currently reproductively isolated Atlantic salmon (Salmo salar) populations (Irish and Norwegian) with a common post-glacial 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 analysing the rate of amino acid replacement in relation to a neutral expectation. Contrary to our prediction, and in contrast to the situation for other genetic markers, the two populations have almost non-overlapping sets of MHC class I alleles. Although there is a strong signal of point mutation that predates population divergence, recent recombination, acting in similar, but not identical, ways in both populations appears to be a significant force in creating new alleles. Moreover, selection acting on peptide binding residues seems to favour new recombinant alleles and is likely to be responsible for the rapid divergence between populations.
Accepted January 25, 2005
Research Article
Rapid Evolution of the MH Class I Locus Results in Different Allelic Compositions in Recently Diverged Populations of Atlantic Salmon
,
,
2 Cell Biology and Immunology Group, Department of Animal Sciences, Wageningen University, Marijkeweg 40, 6709 PG Wageningen, The Netherlands
S. Consuegra, E-mail: sonia.consuegra{at}st-andrews.ac.uk
![]()
Abstract
SC and H-JM equally contributed to this study![]()
CiteULike
Connotea
Del.icio.us What's this?
This article has been cited by other articles:
![]() |
S. E Yeates, S. Einum, I. A Fleming, H.-J. Megens, R. J.M Stet, K. Hindar, W. V Holt, K. J.W Van Look, and M. J.G Gage Atlantic salmon eggs favour sperm in competition that have similar major histocompatibility alleles Proc R Soc B, February 7, 2009; 276(1656): 559 - 566. [Abstract] [Full Text] [PDF] |
||||
![]() |
R. J. Stoffels and H. G. Spencer An Asymmetric Model of Heterozygote Advantage at Major Histocompatibility Complex Genes: Degenerate Pathogen Recognition and Intersection Advantage Genetics, March 1, 2008; 178(3): 1473 - 1489. [Abstract] [Full Text] [PDF] |
||||
![]() |
H. C. Miller, M. Andrews-Cookson, and C. H. Daugherty Two Patterns of Variation among MHC Class I Loci in Tuatara (Sphenodon punctatus) J. Hered., November 21, 2007; (2007) esm095v1. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. Cohen, J. Tirindelli, M. Gomez-Chiarri, and D. Nacci Functional implications of Major Histocompatibility (MH) variation using estuarine fish populations Integr. Comp. Biol., December 1, 2006; 46(6): 1016 - 1029. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. Coughlan, P. McGinnity, B. O'Farrell, E. Dillane, O. Diserud, E. de Eyto, K. Farrell, K. Whelan, R. J.M. Stet, and T. F. Cross Temporal variation in an immune response gene (MHC I) in anadromous Salmo trutta in an Irish river before and during aquaculture activities ICES J. Mar. Sci., January 1, 2006; 63(7): 1248 - 1255. [Abstract] [Full Text] [PDF] |
||||
![]() |
D. H. Bos and B. Waldman Evolution by Recombination and Transspecies Polymorphism in the MHC Class I Gene of Xenopus laevis Mol. Biol. Evol., January 1, 2006; 23(1): 137 - 143. [Abstract] [Full Text] [PDF] |
||||





