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Co-option of an endogenous retrovirus envelope for host defense in hominid ancestors
Endogenous retroviral sequences provide a molecular fossil record of ancient infections whose analysis might illuminate mechanisms of viral extinction. A close relative of gammaretroviruses, HERV-T, circulated in primates for ~25 million years (MY) before apparent extinction within the past ~8 MY. C...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5388530/ https://www.ncbi.nlm.nih.gov/pubmed/28397686 http://dx.doi.org/10.7554/eLife.22519 |
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author | Blanco-Melo, Daniel Gifford, Robert J Bieniasz, Paul D |
author_facet | Blanco-Melo, Daniel Gifford, Robert J Bieniasz, Paul D |
author_sort | Blanco-Melo, Daniel |
collection | PubMed |
description | Endogenous retroviral sequences provide a molecular fossil record of ancient infections whose analysis might illuminate mechanisms of viral extinction. A close relative of gammaretroviruses, HERV-T, circulated in primates for ~25 million years (MY) before apparent extinction within the past ~8 MY. Construction of a near-complete catalog of HERV-T fossils in primate genomes allowed us to estimate a ~32 MY old ancestral sequence and reconstruct a functional envelope protein (ancHTenv) that could support infection of a pseudotyped modern gammaretrovirus. Using ancHTenv, we identify monocarboxylate transporter-1 (MCT-1) as a receptor used by HERV-T for attachment and infection. A single HERV-T provirus in hominid genomes includes an env gene (hsaHTenv) that has been uniquely preserved. This apparently exapted HERV-T env could not support virion infection but could block ancHTenv mediated infection, by causing MCT-1 depletion from cell surfaces. Thus, hsaHTenv may have contributed to HERV-T extinction, and could also potentially regulate cellular metabolism. DOI: http://dx.doi.org/10.7554/eLife.22519.001 |
format | Online Article Text |
id | pubmed-5388530 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-53885302017-04-14 Co-option of an endogenous retrovirus envelope for host defense in hominid ancestors Blanco-Melo, Daniel Gifford, Robert J Bieniasz, Paul D eLife Genomics and Evolutionary Biology Endogenous retroviral sequences provide a molecular fossil record of ancient infections whose analysis might illuminate mechanisms of viral extinction. A close relative of gammaretroviruses, HERV-T, circulated in primates for ~25 million years (MY) before apparent extinction within the past ~8 MY. Construction of a near-complete catalog of HERV-T fossils in primate genomes allowed us to estimate a ~32 MY old ancestral sequence and reconstruct a functional envelope protein (ancHTenv) that could support infection of a pseudotyped modern gammaretrovirus. Using ancHTenv, we identify monocarboxylate transporter-1 (MCT-1) as a receptor used by HERV-T for attachment and infection. A single HERV-T provirus in hominid genomes includes an env gene (hsaHTenv) that has been uniquely preserved. This apparently exapted HERV-T env could not support virion infection but could block ancHTenv mediated infection, by causing MCT-1 depletion from cell surfaces. Thus, hsaHTenv may have contributed to HERV-T extinction, and could also potentially regulate cellular metabolism. DOI: http://dx.doi.org/10.7554/eLife.22519.001 eLife Sciences Publications, Ltd 2017-04-11 /pmc/articles/PMC5388530/ /pubmed/28397686 http://dx.doi.org/10.7554/eLife.22519 Text en © 2017, Blanco-Melo et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Genomics and Evolutionary Biology Blanco-Melo, Daniel Gifford, Robert J Bieniasz, Paul D Co-option of an endogenous retrovirus envelope for host defense in hominid ancestors |
title | Co-option of an endogenous retrovirus envelope for host defense in hominid ancestors |
title_full | Co-option of an endogenous retrovirus envelope for host defense in hominid ancestors |
title_fullStr | Co-option of an endogenous retrovirus envelope for host defense in hominid ancestors |
title_full_unstemmed | Co-option of an endogenous retrovirus envelope for host defense in hominid ancestors |
title_short | Co-option of an endogenous retrovirus envelope for host defense in hominid ancestors |
title_sort | co-option of an endogenous retrovirus envelope for host defense in hominid ancestors |
topic | Genomics and Evolutionary Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5388530/ https://www.ncbi.nlm.nih.gov/pubmed/28397686 http://dx.doi.org/10.7554/eLife.22519 |
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