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Evolution and gene capture in ancient endogenous retroviruses - insights from the crocodilian genomes
BACKGROUND: Crocodilians are thought to be hosts to a diverse and divergent complement of endogenous retroviruses (ERVs) but a comprehensive investigation is yet to be performed. The recent sequencing of three crocodilian genomes provides an opportunity for a more detailed and accurate representatio...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4299795/ https://www.ncbi.nlm.nih.gov/pubmed/25499090 http://dx.doi.org/10.1186/s12977-014-0071-2 |
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author | Chong, Amanda Y Kojima, Kenji K Jurka, Jerzy Ray, David A Smit, Arian F A Isberg, Sally R Gongora, Jaime |
author_facet | Chong, Amanda Y Kojima, Kenji K Jurka, Jerzy Ray, David A Smit, Arian F A Isberg, Sally R Gongora, Jaime |
author_sort | Chong, Amanda Y |
collection | PubMed |
description | BACKGROUND: Crocodilians are thought to be hosts to a diverse and divergent complement of endogenous retroviruses (ERVs) but a comprehensive investigation is yet to be performed. The recent sequencing of three crocodilian genomes provides an opportunity for a more detailed and accurate representation of the ERV diversity that is present in these species. Here we investigate the diversity, distribution and evolution of ERVs from the genomes of three key crocodilian species, and outline the key processes driving crocodilian ERV proliferation and evolution. RESULTS: ERVs and ERV related sequences make up less than 2% of crocodilian genomes. We recovered and described 45 ERV groups within the three crocodilian genomes, many of which are species specific. We have also revealed a new class of ERV, ERV4, which appears to be common to crocodilians and turtles, and currently has no characterised exogenous counterpart. For the first time, we formally describe the characteristics of this ERV class and its classification relative to other recognised ERV and retroviral classes. This class shares some sequence similarity and sequence characteristics with ERV3, although it is phylogenetically distinct from the other ERV classes. We have also identified two instances of gene capture by crocodilian ERVs, one of which, the capture of a host KIT-ligand mRNA has occurred without the loss of an ERV domain. CONCLUSIONS: This study indicates that crocodilian ERVs comprise a wide variety of lineages, many of which appear to reflect ancient infections. In particular, ERV4 appears to have a limited host range, with current data suggesting that it is confined to crocodilians and some lineages of turtles. Also of interest are two ERV groups that demonstrate evidence of host gene capture. This study provides a framework to facilitate further studies into non-mammalian vertebrates and highlights the need for further studies into such species. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12977-014-0071-2) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4299795 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-42997952015-01-21 Evolution and gene capture in ancient endogenous retroviruses - insights from the crocodilian genomes Chong, Amanda Y Kojima, Kenji K Jurka, Jerzy Ray, David A Smit, Arian F A Isberg, Sally R Gongora, Jaime Retrovirology Research BACKGROUND: Crocodilians are thought to be hosts to a diverse and divergent complement of endogenous retroviruses (ERVs) but a comprehensive investigation is yet to be performed. The recent sequencing of three crocodilian genomes provides an opportunity for a more detailed and accurate representation of the ERV diversity that is present in these species. Here we investigate the diversity, distribution and evolution of ERVs from the genomes of three key crocodilian species, and outline the key processes driving crocodilian ERV proliferation and evolution. RESULTS: ERVs and ERV related sequences make up less than 2% of crocodilian genomes. We recovered and described 45 ERV groups within the three crocodilian genomes, many of which are species specific. We have also revealed a new class of ERV, ERV4, which appears to be common to crocodilians and turtles, and currently has no characterised exogenous counterpart. For the first time, we formally describe the characteristics of this ERV class and its classification relative to other recognised ERV and retroviral classes. This class shares some sequence similarity and sequence characteristics with ERV3, although it is phylogenetically distinct from the other ERV classes. We have also identified two instances of gene capture by crocodilian ERVs, one of which, the capture of a host KIT-ligand mRNA has occurred without the loss of an ERV domain. CONCLUSIONS: This study indicates that crocodilian ERVs comprise a wide variety of lineages, many of which appear to reflect ancient infections. In particular, ERV4 appears to have a limited host range, with current data suggesting that it is confined to crocodilians and some lineages of turtles. Also of interest are two ERV groups that demonstrate evidence of host gene capture. This study provides a framework to facilitate further studies into non-mammalian vertebrates and highlights the need for further studies into such species. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12977-014-0071-2) contains supplementary material, which is available to authorized users. BioMed Central 2014-12-12 /pmc/articles/PMC4299795/ /pubmed/25499090 http://dx.doi.org/10.1186/s12977-014-0071-2 Text en © Chong et al.; licensee BioMed Central. 2014 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 credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Chong, Amanda Y Kojima, Kenji K Jurka, Jerzy Ray, David A Smit, Arian F A Isberg, Sally R Gongora, Jaime Evolution and gene capture in ancient endogenous retroviruses - insights from the crocodilian genomes |
title | Evolution and gene capture in ancient endogenous retroviruses - insights from the crocodilian genomes |
title_full | Evolution and gene capture in ancient endogenous retroviruses - insights from the crocodilian genomes |
title_fullStr | Evolution and gene capture in ancient endogenous retroviruses - insights from the crocodilian genomes |
title_full_unstemmed | Evolution and gene capture in ancient endogenous retroviruses - insights from the crocodilian genomes |
title_short | Evolution and gene capture in ancient endogenous retroviruses - insights from the crocodilian genomes |
title_sort | evolution and gene capture in ancient endogenous retroviruses - insights from the crocodilian genomes |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4299795/ https://www.ncbi.nlm.nih.gov/pubmed/25499090 http://dx.doi.org/10.1186/s12977-014-0071-2 |
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