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Gene conversion and purifying selection of a placenta-specific ERV-V envelope gene during simian evolution
BACKGROUND: Most human endogenous retroviruses (HERVs) invaded our genome at least 25 million years ago. The majority of the viral genes are degenerated, since no selection preserves them within the genome. However, a few intact and very old HERV genes exist, and likely are beneficial for the host....
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2567338/ https://www.ncbi.nlm.nih.gov/pubmed/18826608 http://dx.doi.org/10.1186/1471-2148-8-266 |
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author | Kjeldbjerg, Anders L Villesen, Palle Aagaard, Lars Pedersen, Finn Skou |
author_facet | Kjeldbjerg, Anders L Villesen, Palle Aagaard, Lars Pedersen, Finn Skou |
author_sort | Kjeldbjerg, Anders L |
collection | PubMed |
description | BACKGROUND: Most human endogenous retroviruses (HERVs) invaded our genome at least 25 million years ago. The majority of the viral genes are degenerated, since no selection preserves them within the genome. However, a few intact and very old HERV genes exist, and likely are beneficial for the host. We here address evolutionary aspects of two HERV-V envelope genes, ENVV1 and ENVV2, located in tandem and containing a long open reading frame. RESULTS: The ENVV2 gene is preserved with an intact reading frame during simian evolution, but none of the ENVV genes are found in the prosimian species tested. While we observe many transposon insertions in the gag and pol regions of the ERV-V2 provirus, the ENVV2 genes have escaped transposon crossfire in all species tested. Additional analysis of nucleotide substitutions provides further strong evidence of purifying selection on the ENVV2 gene during primate evolution. The other copy, ENVV1, seems to be involved in gene conversion of the major part of the envelope. Furthermore, ENVV1 and ENVV2 show placenta-specific expression in human and a baboon species. CONCLUSION: Our analyses show that ERV-V entered our genome after the split between simian and prosimian primates. Subsequent purifying selection and gene conversion have preserved two copies of the ENVV envelope gene in most species. This is the first case of gene conversion involving long open reading frames in HERVs. Together with the placenta-specific expression of the human and baboon ENVV1 and ENVV2 envelope genes, these data provide strong evidence of a beneficial role for the host. |
format | Text |
id | pubmed-2567338 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-25673382008-10-15 Gene conversion and purifying selection of a placenta-specific ERV-V envelope gene during simian evolution Kjeldbjerg, Anders L Villesen, Palle Aagaard, Lars Pedersen, Finn Skou BMC Evol Biol Research Article BACKGROUND: Most human endogenous retroviruses (HERVs) invaded our genome at least 25 million years ago. The majority of the viral genes are degenerated, since no selection preserves them within the genome. However, a few intact and very old HERV genes exist, and likely are beneficial for the host. We here address evolutionary aspects of two HERV-V envelope genes, ENVV1 and ENVV2, located in tandem and containing a long open reading frame. RESULTS: The ENVV2 gene is preserved with an intact reading frame during simian evolution, but none of the ENVV genes are found in the prosimian species tested. While we observe many transposon insertions in the gag and pol regions of the ERV-V2 provirus, the ENVV2 genes have escaped transposon crossfire in all species tested. Additional analysis of nucleotide substitutions provides further strong evidence of purifying selection on the ENVV2 gene during primate evolution. The other copy, ENVV1, seems to be involved in gene conversion of the major part of the envelope. Furthermore, ENVV1 and ENVV2 show placenta-specific expression in human and a baboon species. CONCLUSION: Our analyses show that ERV-V entered our genome after the split between simian and prosimian primates. Subsequent purifying selection and gene conversion have preserved two copies of the ENVV envelope gene in most species. This is the first case of gene conversion involving long open reading frames in HERVs. Together with the placenta-specific expression of the human and baboon ENVV1 and ENVV2 envelope genes, these data provide strong evidence of a beneficial role for the host. BioMed Central 2008-09-30 /pmc/articles/PMC2567338/ /pubmed/18826608 http://dx.doi.org/10.1186/1471-2148-8-266 Text en Copyright ©2008 Kjeldbjerg 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 Kjeldbjerg, Anders L Villesen, Palle Aagaard, Lars Pedersen, Finn Skou Gene conversion and purifying selection of a placenta-specific ERV-V envelope gene during simian evolution |
title | Gene conversion and purifying selection of a placenta-specific ERV-V envelope gene during simian evolution |
title_full | Gene conversion and purifying selection of a placenta-specific ERV-V envelope gene during simian evolution |
title_fullStr | Gene conversion and purifying selection of a placenta-specific ERV-V envelope gene during simian evolution |
title_full_unstemmed | Gene conversion and purifying selection of a placenta-specific ERV-V envelope gene during simian evolution |
title_short | Gene conversion and purifying selection of a placenta-specific ERV-V envelope gene during simian evolution |
title_sort | gene conversion and purifying selection of a placenta-specific erv-v envelope gene during simian evolution |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2567338/ https://www.ncbi.nlm.nih.gov/pubmed/18826608 http://dx.doi.org/10.1186/1471-2148-8-266 |
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