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Structure and Diversity of the Rhesus Macaque Immunoglobulin Loci through Multiple De Novo Genome Assemblies
The rhesus macaque is a critically important animal model in biomedical research, most recently playing a key role in the development of vaccines against human immunodeficiency virus-1. Nevertheless, the immunoglobulin (Ig) loci of macaques are as yet incompletely determined and our understanding of...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2017
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5663730/ https://www.ncbi.nlm.nih.gov/pubmed/29163486 http://dx.doi.org/10.3389/fimmu.2017.01407 |
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author | Ramesh, Akshaya Darko, Sam Hua, Axin Overman, Glenn Ransier, Amy Francica, Joseph R. Trama, Ashley Tomaras, Georgia D. Haynes, Barton F. Douek, Daniel C. Kepler, Thomas B. |
author_facet | Ramesh, Akshaya Darko, Sam Hua, Axin Overman, Glenn Ransier, Amy Francica, Joseph R. Trama, Ashley Tomaras, Georgia D. Haynes, Barton F. Douek, Daniel C. Kepler, Thomas B. |
author_sort | Ramesh, Akshaya |
collection | PubMed |
description | The rhesus macaque is a critically important animal model in biomedical research, most recently playing a key role in the development of vaccines against human immunodeficiency virus-1. Nevertheless, the immunoglobulin (Ig) loci of macaques are as yet incompletely determined and our understanding of differences between human and macaque humoral immunity remains deficient. We completed a high-coverage, high-quality whole genome sequencing and assembly project with a single rhesus macaque of Indian origin, and partial genome assemblies using genomic molecular targeting of the Ig loci in nine other rhesus macaques of Indian origin. These data indicate that the macaque Ig loci are substantially more diverse than those in humans, including greater sequence diversity and copy-number variation between individuals. It appears likely that such copy-number variation even occurs between allelic loci within individuals. Different Ig gene families in the macaque show distinct relationships to the corresponding human gene families and appear to evolve under different mechanisms. These results raise intriguing questions about the evolution of antigen receptors in primates but also have important practical implications for the design and interpretation of biomedical studies. |
format | Online Article Text |
id | pubmed-5663730 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-56637302017-11-21 Structure and Diversity of the Rhesus Macaque Immunoglobulin Loci through Multiple De Novo Genome Assemblies Ramesh, Akshaya Darko, Sam Hua, Axin Overman, Glenn Ransier, Amy Francica, Joseph R. Trama, Ashley Tomaras, Georgia D. Haynes, Barton F. Douek, Daniel C. Kepler, Thomas B. Front Immunol Immunology The rhesus macaque is a critically important animal model in biomedical research, most recently playing a key role in the development of vaccines against human immunodeficiency virus-1. Nevertheless, the immunoglobulin (Ig) loci of macaques are as yet incompletely determined and our understanding of differences between human and macaque humoral immunity remains deficient. We completed a high-coverage, high-quality whole genome sequencing and assembly project with a single rhesus macaque of Indian origin, and partial genome assemblies using genomic molecular targeting of the Ig loci in nine other rhesus macaques of Indian origin. These data indicate that the macaque Ig loci are substantially more diverse than those in humans, including greater sequence diversity and copy-number variation between individuals. It appears likely that such copy-number variation even occurs between allelic loci within individuals. Different Ig gene families in the macaque show distinct relationships to the corresponding human gene families and appear to evolve under different mechanisms. These results raise intriguing questions about the evolution of antigen receptors in primates but also have important practical implications for the design and interpretation of biomedical studies. Frontiers Media S.A. 2017-10-27 /pmc/articles/PMC5663730/ /pubmed/29163486 http://dx.doi.org/10.3389/fimmu.2017.01407 Text en Copyright © 2017 Ramesh, Darko, Hua, Overman, Ransier, Francica, Trama, Tomaras, Haynes, Douek and Kepler. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Immunology Ramesh, Akshaya Darko, Sam Hua, Axin Overman, Glenn Ransier, Amy Francica, Joseph R. Trama, Ashley Tomaras, Georgia D. Haynes, Barton F. Douek, Daniel C. Kepler, Thomas B. Structure and Diversity of the Rhesus Macaque Immunoglobulin Loci through Multiple De Novo Genome Assemblies |
title | Structure and Diversity of the Rhesus Macaque Immunoglobulin Loci through Multiple De Novo Genome Assemblies |
title_full | Structure and Diversity of the Rhesus Macaque Immunoglobulin Loci through Multiple De Novo Genome Assemblies |
title_fullStr | Structure and Diversity of the Rhesus Macaque Immunoglobulin Loci through Multiple De Novo Genome Assemblies |
title_full_unstemmed | Structure and Diversity of the Rhesus Macaque Immunoglobulin Loci through Multiple De Novo Genome Assemblies |
title_short | Structure and Diversity of the Rhesus Macaque Immunoglobulin Loci through Multiple De Novo Genome Assemblies |
title_sort | structure and diversity of the rhesus macaque immunoglobulin loci through multiple de novo genome assemblies |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5663730/ https://www.ncbi.nlm.nih.gov/pubmed/29163486 http://dx.doi.org/10.3389/fimmu.2017.01407 |
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