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Evolution and comparative analysis of the bat MHC-I region

Bats are natural hosts to numerous viruses and have ancient origins, having diverged from other eutherian mammals early in evolution. These characteristics place them in an important position to provide insights into the evolution of the mammalian immune system and antiviral immunity. We describe th...

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Autores principales: Ng, Justin H. J., Tachedjian, Mary, Deakin, Janine, Wynne, James W., Cui, Jie, Haring, Volker, Broz, Ivano, Chen, Honglei, Belov, Katherine, Wang, Lin-Fa, Baker, Michelle L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4753418/
https://www.ncbi.nlm.nih.gov/pubmed/26876644
http://dx.doi.org/10.1038/srep21256
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author Ng, Justin H. J.
Tachedjian, Mary
Deakin, Janine
Wynne, James W.
Cui, Jie
Haring, Volker
Broz, Ivano
Chen, Honglei
Belov, Katherine
Wang, Lin-Fa
Baker, Michelle L.
author_facet Ng, Justin H. J.
Tachedjian, Mary
Deakin, Janine
Wynne, James W.
Cui, Jie
Haring, Volker
Broz, Ivano
Chen, Honglei
Belov, Katherine
Wang, Lin-Fa
Baker, Michelle L.
author_sort Ng, Justin H. J.
collection PubMed
description Bats are natural hosts to numerous viruses and have ancient origins, having diverged from other eutherian mammals early in evolution. These characteristics place them in an important position to provide insights into the evolution of the mammalian immune system and antiviral immunity. We describe the first detailed partial map of a bat (Pteropus alecto) MHC-I region with comparative analysis of the MHC-I region and genes. The bat MHC-I region is highly condensed, yet relatively conserved in organisation, and is unusual in that MHC-I genes are present within only one of the three highly conserved class I duplication blocks. We hypothesise that MHC-I genes first originated in the β duplication block, and subsequently duplicated in a step-wise manner across the MHC-I region during mammalian evolution. Furthermore, bat MHC-I genes contain unique insertions within their peptide-binding grooves potentially affecting the peptide repertoire presented to T cells, which may have implications for the ability of bats to control infection without overt disease.
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spelling pubmed-47534182016-02-23 Evolution and comparative analysis of the bat MHC-I region Ng, Justin H. J. Tachedjian, Mary Deakin, Janine Wynne, James W. Cui, Jie Haring, Volker Broz, Ivano Chen, Honglei Belov, Katherine Wang, Lin-Fa Baker, Michelle L. Sci Rep Article Bats are natural hosts to numerous viruses and have ancient origins, having diverged from other eutherian mammals early in evolution. These characteristics place them in an important position to provide insights into the evolution of the mammalian immune system and antiviral immunity. We describe the first detailed partial map of a bat (Pteropus alecto) MHC-I region with comparative analysis of the MHC-I region and genes. The bat MHC-I region is highly condensed, yet relatively conserved in organisation, and is unusual in that MHC-I genes are present within only one of the three highly conserved class I duplication blocks. We hypothesise that MHC-I genes first originated in the β duplication block, and subsequently duplicated in a step-wise manner across the MHC-I region during mammalian evolution. Furthermore, bat MHC-I genes contain unique insertions within their peptide-binding grooves potentially affecting the peptide repertoire presented to T cells, which may have implications for the ability of bats to control infection without overt disease. Nature Publishing Group 2016-02-15 /pmc/articles/PMC4753418/ /pubmed/26876644 http://dx.doi.org/10.1038/srep21256 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Ng, Justin H. J.
Tachedjian, Mary
Deakin, Janine
Wynne, James W.
Cui, Jie
Haring, Volker
Broz, Ivano
Chen, Honglei
Belov, Katherine
Wang, Lin-Fa
Baker, Michelle L.
Evolution and comparative analysis of the bat MHC-I region
title Evolution and comparative analysis of the bat MHC-I region
title_full Evolution and comparative analysis of the bat MHC-I region
title_fullStr Evolution and comparative analysis of the bat MHC-I region
title_full_unstemmed Evolution and comparative analysis of the bat MHC-I region
title_short Evolution and comparative analysis of the bat MHC-I region
title_sort evolution and comparative analysis of the bat mhc-i region
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4753418/
https://www.ncbi.nlm.nih.gov/pubmed/26876644
http://dx.doi.org/10.1038/srep21256
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