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Gene duplication and fragmentation in the zebra finch major histocompatibility complex

BACKGROUND: Due to its high polymorphism and importance for disease resistance, the major histocompatibility complex (MHC) has been an important focus of many vertebrate genome projects. Avian MHC organization is of particular interest because the chicken Gallus gallus, the avian species with the be...

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Autores principales: Balakrishnan, Christopher N, Ekblom, Robert, Völker, Martin, Westerdahl, Helena, Godinez, Ricardo, Kotkiewicz, Holly, Burt, David W, Graves, Tina, Griffin, Darren K, Warren, Wesley C, Edwards, Scott V
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2907588/
https://www.ncbi.nlm.nih.gov/pubmed/20359332
http://dx.doi.org/10.1186/1741-7007-8-29
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author Balakrishnan, Christopher N
Ekblom, Robert
Völker, Martin
Westerdahl, Helena
Godinez, Ricardo
Kotkiewicz, Holly
Burt, David W
Graves, Tina
Griffin, Darren K
Warren, Wesley C
Edwards, Scott V
author_facet Balakrishnan, Christopher N
Ekblom, Robert
Völker, Martin
Westerdahl, Helena
Godinez, Ricardo
Kotkiewicz, Holly
Burt, David W
Graves, Tina
Griffin, Darren K
Warren, Wesley C
Edwards, Scott V
author_sort Balakrishnan, Christopher N
collection PubMed
description BACKGROUND: Due to its high polymorphism and importance for disease resistance, the major histocompatibility complex (MHC) has been an important focus of many vertebrate genome projects. Avian MHC organization is of particular interest because the chicken Gallus gallus, the avian species with the best characterized MHC, possesses a highly streamlined minimal essential MHC, which is linked to resistance against specific pathogens. It remains unclear the extent to which this organization describes the situation in other birds and whether it represents a derived or ancestral condition. The sequencing of the zebra finch Taeniopygia guttata genome, in combination with targeted bacterial artificial chromosome (BAC) sequencing, has allowed us to characterize an MHC from a highly divergent and diverse avian lineage, the passerines. RESULTS: The zebra finch MHC exhibits a complex structure and history involving gene duplication and fragmentation. The zebra finch MHC includes multiple Class I and Class II genes, some of which appear to be pseudogenes, and spans a much more extensive genomic region than the chicken MHC, as evidenced by the presence of MHC genes on each of seven BACs spanning 739 kb. Cytogenetic (FISH) evidence and the genome assembly itself place core MHC genes on as many as four chromosomes with TAP and Class I genes mapping to different chromosomes. MHC Class II regions are further characterized by high endogenous retroviral content. Lastly, we find strong evidence of selection acting on sites within passerine MHC Class I and Class II genes. CONCLUSION: The zebra finch MHC differs markedly from that of the chicken, the only other bird species with a complete genome sequence. The apparent lack of synteny between TAP and the expressed MHC Class I locus is in fact reminiscent of a pattern seen in some mammalian lineages and may represent convergent evolution. Our analyses of the zebra finch MHC suggest a complex history involving chromosomal fission, gene duplication and translocation in the history of the MHC in birds, and highlight striking differences in MHC structure and organization among avian lineages.
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spelling pubmed-29075882010-07-22 Gene duplication and fragmentation in the zebra finch major histocompatibility complex Balakrishnan, Christopher N Ekblom, Robert Völker, Martin Westerdahl, Helena Godinez, Ricardo Kotkiewicz, Holly Burt, David W Graves, Tina Griffin, Darren K Warren, Wesley C Edwards, Scott V BMC Biol Research article BACKGROUND: Due to its high polymorphism and importance for disease resistance, the major histocompatibility complex (MHC) has been an important focus of many vertebrate genome projects. Avian MHC organization is of particular interest because the chicken Gallus gallus, the avian species with the best characterized MHC, possesses a highly streamlined minimal essential MHC, which is linked to resistance against specific pathogens. It remains unclear the extent to which this organization describes the situation in other birds and whether it represents a derived or ancestral condition. The sequencing of the zebra finch Taeniopygia guttata genome, in combination with targeted bacterial artificial chromosome (BAC) sequencing, has allowed us to characterize an MHC from a highly divergent and diverse avian lineage, the passerines. RESULTS: The zebra finch MHC exhibits a complex structure and history involving gene duplication and fragmentation. The zebra finch MHC includes multiple Class I and Class II genes, some of which appear to be pseudogenes, and spans a much more extensive genomic region than the chicken MHC, as evidenced by the presence of MHC genes on each of seven BACs spanning 739 kb. Cytogenetic (FISH) evidence and the genome assembly itself place core MHC genes on as many as four chromosomes with TAP and Class I genes mapping to different chromosomes. MHC Class II regions are further characterized by high endogenous retroviral content. Lastly, we find strong evidence of selection acting on sites within passerine MHC Class I and Class II genes. CONCLUSION: The zebra finch MHC differs markedly from that of the chicken, the only other bird species with a complete genome sequence. The apparent lack of synteny between TAP and the expressed MHC Class I locus is in fact reminiscent of a pattern seen in some mammalian lineages and may represent convergent evolution. Our analyses of the zebra finch MHC suggest a complex history involving chromosomal fission, gene duplication and translocation in the history of the MHC in birds, and highlight striking differences in MHC structure and organization among avian lineages. BioMed Central 2010-04-01 /pmc/articles/PMC2907588/ /pubmed/20359332 http://dx.doi.org/10.1186/1741-7007-8-29 Text en Copyright ©2010 Balakrishnan et al; 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 article
Balakrishnan, Christopher N
Ekblom, Robert
Völker, Martin
Westerdahl, Helena
Godinez, Ricardo
Kotkiewicz, Holly
Burt, David W
Graves, Tina
Griffin, Darren K
Warren, Wesley C
Edwards, Scott V
Gene duplication and fragmentation in the zebra finch major histocompatibility complex
title Gene duplication and fragmentation in the zebra finch major histocompatibility complex
title_full Gene duplication and fragmentation in the zebra finch major histocompatibility complex
title_fullStr Gene duplication and fragmentation in the zebra finch major histocompatibility complex
title_full_unstemmed Gene duplication and fragmentation in the zebra finch major histocompatibility complex
title_short Gene duplication and fragmentation in the zebra finch major histocompatibility complex
title_sort gene duplication and fragmentation in the zebra finch major histocompatibility complex
topic Research article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2907588/
https://www.ncbi.nlm.nih.gov/pubmed/20359332
http://dx.doi.org/10.1186/1741-7007-8-29
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