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The orthology of HLA-E and H2-Qa1 is hidden by their concerted evolution with other MHC class I molecules
BACKGROUND: Whether MHC molecules undergo concerted evolution or not has been the subject of a long-standing debate. RESULTS: By comparing sequences of eight functional homologues of HLA-E from primates and rodents with those of MHC class Ia molecules from the same eight species, we find that differ...
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2006
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1403747/ https://www.ncbi.nlm.nih.gov/pubmed/16542007 http://dx.doi.org/10.1186/1745-6150-1-2 |
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author | Joly, Etienne Rouillon, Virginie |
author_facet | Joly, Etienne Rouillon, Virginie |
author_sort | Joly, Etienne |
collection | PubMed |
description | BACKGROUND: Whether MHC molecules undergo concerted evolution or not has been the subject of a long-standing debate. RESULTS: By comparing sequences of eight functional homologues of HLA-E from primates and rodents with those of MHC class Ia molecules from the same eight species, we find that different portions of MHC class I molecules undergo different patterns of evolution. By focusing our analyses sequentially on these various portions, we have obtained clear evidence for concerted evolution of MHC class I molecules, suggesting the occurrence of extensive interallelic and intergenic exchanges. Intra-species homogenisation of sequences is particularly noticeable at the level of exon 4, which codes for the α3 domain, but our results suggest that homogenisation also concerns certain residues of the α1–α2 codomain that lie outside the antigen recognition site. CONCLUSION: A model is presented in which Darwinian selective pressures due to pathogens could, at the same time, favour diversification of MHC class Ia molecules and promote concerted evolution of separate loci by spreading advantageous motifs arising by mutations in individual MHC molecules to other alleles and to other loci of the MHC region. This would also allow MHC molecules to co-evolve with the proteins with which they interact to fulfil their functions of antigen presentation and regulation of NK cell activity. One of the raisons d'être of the MHC may therefore be to favour at the same time both diversification of MHC class Ia molecules and homogenisation of the whole pool of MHC class I molecules (Ia and Ib) involved in antigen presentation. REVIEWERS: This article was reviewed by Stephan Beck, Lutz Walter and Pierre Pontarotti. |
format | Text |
id | pubmed-1403747 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2006 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-14037472006-03-18 The orthology of HLA-E and H2-Qa1 is hidden by their concerted evolution with other MHC class I molecules Joly, Etienne Rouillon, Virginie Biol Direct Research BACKGROUND: Whether MHC molecules undergo concerted evolution or not has been the subject of a long-standing debate. RESULTS: By comparing sequences of eight functional homologues of HLA-E from primates and rodents with those of MHC class Ia molecules from the same eight species, we find that different portions of MHC class I molecules undergo different patterns of evolution. By focusing our analyses sequentially on these various portions, we have obtained clear evidence for concerted evolution of MHC class I molecules, suggesting the occurrence of extensive interallelic and intergenic exchanges. Intra-species homogenisation of sequences is particularly noticeable at the level of exon 4, which codes for the α3 domain, but our results suggest that homogenisation also concerns certain residues of the α1–α2 codomain that lie outside the antigen recognition site. CONCLUSION: A model is presented in which Darwinian selective pressures due to pathogens could, at the same time, favour diversification of MHC class Ia molecules and promote concerted evolution of separate loci by spreading advantageous motifs arising by mutations in individual MHC molecules to other alleles and to other loci of the MHC region. This would also allow MHC molecules to co-evolve with the proteins with which they interact to fulfil their functions of antigen presentation and regulation of NK cell activity. One of the raisons d'être of the MHC may therefore be to favour at the same time both diversification of MHC class Ia molecules and homogenisation of the whole pool of MHC class I molecules (Ia and Ib) involved in antigen presentation. REVIEWERS: This article was reviewed by Stephan Beck, Lutz Walter and Pierre Pontarotti. BioMed Central 2006-01-31 /pmc/articles/PMC1403747/ /pubmed/16542007 http://dx.doi.org/10.1186/1745-6150-1-2 Text en Copyright © 2006 Joly and Rouillon; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Joly, Etienne Rouillon, Virginie The orthology of HLA-E and H2-Qa1 is hidden by their concerted evolution with other MHC class I molecules |
title | The orthology of HLA-E and H2-Qa1 is hidden by their concerted evolution with other MHC class I molecules |
title_full | The orthology of HLA-E and H2-Qa1 is hidden by their concerted evolution with other MHC class I molecules |
title_fullStr | The orthology of HLA-E and H2-Qa1 is hidden by their concerted evolution with other MHC class I molecules |
title_full_unstemmed | The orthology of HLA-E and H2-Qa1 is hidden by their concerted evolution with other MHC class I molecules |
title_short | The orthology of HLA-E and H2-Qa1 is hidden by their concerted evolution with other MHC class I molecules |
title_sort | orthology of hla-e and h2-qa1 is hidden by their concerted evolution with other mhc class i molecules |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1403747/ https://www.ncbi.nlm.nih.gov/pubmed/16542007 http://dx.doi.org/10.1186/1745-6150-1-2 |
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