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Evolutionary genetics of immunological supertypes reveals two faces of the Red Queen

Red Queen host–parasite co-evolution can drive adaptations of immune genes by positive selection that erodes genetic variation (Red Queen arms race) or results in a balanced polymorphism (Red Queen dynamics) and long-term preservation of genetic variation (trans-species polymorphism). These two Red...

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Autores principales: Lighten, Jackie, Papadopulos, Alexander S. T., Mohammed, Ryan S., Ward, Ben J., G. Paterson, Ian, Baillie, Lyndsey, Bradbury, Ian R., Hendry, Andrew P., Bentzen, Paul, van Oosterhout, Cock
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5670221/
https://www.ncbi.nlm.nih.gov/pubmed/29101318
http://dx.doi.org/10.1038/s41467-017-01183-2
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author Lighten, Jackie
Papadopulos, Alexander S. T.
Mohammed, Ryan S.
Ward, Ben J.
G. Paterson, Ian
Baillie, Lyndsey
Bradbury, Ian R.
Hendry, Andrew P.
Bentzen, Paul
van Oosterhout, Cock
author_facet Lighten, Jackie
Papadopulos, Alexander S. T.
Mohammed, Ryan S.
Ward, Ben J.
G. Paterson, Ian
Baillie, Lyndsey
Bradbury, Ian R.
Hendry, Andrew P.
Bentzen, Paul
van Oosterhout, Cock
author_sort Lighten, Jackie
collection PubMed
description Red Queen host–parasite co-evolution can drive adaptations of immune genes by positive selection that erodes genetic variation (Red Queen arms race) or results in a balanced polymorphism (Red Queen dynamics) and long-term preservation of genetic variation (trans-species polymorphism). These two Red Queen processes are opposite extremes of the co-evolutionary spectrum. Here we show that both Red Queen processes can operate simultaneously by analysing the major histocompatibility complex (MHC) in guppies (Poecilia reticulata and P. obscura) and swamp guppies (Micropoecilia picta). Sub-functionalisation of MHC alleles into ‘supertypes’ explains how polymorphisms persist during rapid host–parasite co-evolution. Simulations show the maintenance of supertypes as balanced polymorphisms, consistent with Red Queen dynamics, whereas alleles within supertypes are subject to positive selection in a Red Queen arms race. Building on the divergent allele advantage hypothesis, we show that functional aspects of allelic diversity help to elucidate the evolution of polymorphic genes involved in Red Queen co-evolution.
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spelling pubmed-56702212017-11-07 Evolutionary genetics of immunological supertypes reveals two faces of the Red Queen Lighten, Jackie Papadopulos, Alexander S. T. Mohammed, Ryan S. Ward, Ben J. G. Paterson, Ian Baillie, Lyndsey Bradbury, Ian R. Hendry, Andrew P. Bentzen, Paul van Oosterhout, Cock Nat Commun Article Red Queen host–parasite co-evolution can drive adaptations of immune genes by positive selection that erodes genetic variation (Red Queen arms race) or results in a balanced polymorphism (Red Queen dynamics) and long-term preservation of genetic variation (trans-species polymorphism). These two Red Queen processes are opposite extremes of the co-evolutionary spectrum. Here we show that both Red Queen processes can operate simultaneously by analysing the major histocompatibility complex (MHC) in guppies (Poecilia reticulata and P. obscura) and swamp guppies (Micropoecilia picta). Sub-functionalisation of MHC alleles into ‘supertypes’ explains how polymorphisms persist during rapid host–parasite co-evolution. Simulations show the maintenance of supertypes as balanced polymorphisms, consistent with Red Queen dynamics, whereas alleles within supertypes are subject to positive selection in a Red Queen arms race. Building on the divergent allele advantage hypothesis, we show that functional aspects of allelic diversity help to elucidate the evolution of polymorphic genes involved in Red Queen co-evolution. Nature Publishing Group UK 2017-11-03 /pmc/articles/PMC5670221/ /pubmed/29101318 http://dx.doi.org/10.1038/s41467-017-01183-2 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Lighten, Jackie
Papadopulos, Alexander S. T.
Mohammed, Ryan S.
Ward, Ben J.
G. Paterson, Ian
Baillie, Lyndsey
Bradbury, Ian R.
Hendry, Andrew P.
Bentzen, Paul
van Oosterhout, Cock
Evolutionary genetics of immunological supertypes reveals two faces of the Red Queen
title Evolutionary genetics of immunological supertypes reveals two faces of the Red Queen
title_full Evolutionary genetics of immunological supertypes reveals two faces of the Red Queen
title_fullStr Evolutionary genetics of immunological supertypes reveals two faces of the Red Queen
title_full_unstemmed Evolutionary genetics of immunological supertypes reveals two faces of the Red Queen
title_short Evolutionary genetics of immunological supertypes reveals two faces of the Red Queen
title_sort evolutionary genetics of immunological supertypes reveals two faces of the red queen
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5670221/
https://www.ncbi.nlm.nih.gov/pubmed/29101318
http://dx.doi.org/10.1038/s41467-017-01183-2
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