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The evolution of animal Argonautes: evidence for the absence of antiviral AGO Argonautes in vertebrates
In addition to mediating regulation of endogenous gene expression, RNA interference (RNAi) in plants and invertebrates plays a crucial role in defense against viruses via virus-specific siRNAs. Different studies have demonstrated that the functional diversity of RNAi in animals is linked to the dive...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5569025/ https://www.ncbi.nlm.nih.gov/pubmed/28835645 http://dx.doi.org/10.1038/s41598-017-08043-5 |
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author | Wynant, Niels Santos, Dulce Vanden Broeck, Jozef |
author_facet | Wynant, Niels Santos, Dulce Vanden Broeck, Jozef |
author_sort | Wynant, Niels |
collection | PubMed |
description | In addition to mediating regulation of endogenous gene expression, RNA interference (RNAi) in plants and invertebrates plays a crucial role in defense against viruses via virus-specific siRNAs. Different studies have demonstrated that the functional diversity of RNAi in animals is linked to the diversification of the Argonaute superfamily, central components of RISCs (RNA induced silencing complexes). The animal Argonaute superfamily is traditionally grouped into AGO and PIWI Argonautes. Yet, by performing phylogenetic analyses and determining the selective evolutionary pressure in the metazoan Argonaute superfamily, we provide evidence for the existence of three conserved Argonaute lineages between basal metazoans and protostomes, namely siRNA-class AGO, miRNA-class AGO and PIWI Argonautes. In addition, it shown that the siRNA-class AGO lineage is characterized by high rates of molecular evolution, suggesting a role in the arms race with viruses, while the miRNA-class AGOs display strong sequence conservation. Interestingly, we also demonstrate that vertebrates lack siRNA-class AGO proteins and that vertebrate AGOs display low rates of molecular evolution. In this way, we provide supportive evidence for the loss of the antiviral siRNA-class AGO group in vertebrates and discuss the consequence hereof on antiviral immunity and the use of RNAi as a loss of function tool in these animals. |
format | Online Article Text |
id | pubmed-5569025 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-55690252017-09-01 The evolution of animal Argonautes: evidence for the absence of antiviral AGO Argonautes in vertebrates Wynant, Niels Santos, Dulce Vanden Broeck, Jozef Sci Rep Article In addition to mediating regulation of endogenous gene expression, RNA interference (RNAi) in plants and invertebrates plays a crucial role in defense against viruses via virus-specific siRNAs. Different studies have demonstrated that the functional diversity of RNAi in animals is linked to the diversification of the Argonaute superfamily, central components of RISCs (RNA induced silencing complexes). The animal Argonaute superfamily is traditionally grouped into AGO and PIWI Argonautes. Yet, by performing phylogenetic analyses and determining the selective evolutionary pressure in the metazoan Argonaute superfamily, we provide evidence for the existence of three conserved Argonaute lineages between basal metazoans and protostomes, namely siRNA-class AGO, miRNA-class AGO and PIWI Argonautes. In addition, it shown that the siRNA-class AGO lineage is characterized by high rates of molecular evolution, suggesting a role in the arms race with viruses, while the miRNA-class AGOs display strong sequence conservation. Interestingly, we also demonstrate that vertebrates lack siRNA-class AGO proteins and that vertebrate AGOs display low rates of molecular evolution. In this way, we provide supportive evidence for the loss of the antiviral siRNA-class AGO group in vertebrates and discuss the consequence hereof on antiviral immunity and the use of RNAi as a loss of function tool in these animals. Nature Publishing Group UK 2017-08-23 /pmc/articles/PMC5569025/ /pubmed/28835645 http://dx.doi.org/10.1038/s41598-017-08043-5 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Wynant, Niels Santos, Dulce Vanden Broeck, Jozef The evolution of animal Argonautes: evidence for the absence of antiviral AGO Argonautes in vertebrates |
title | The evolution of animal Argonautes: evidence for the absence of antiviral AGO Argonautes in vertebrates |
title_full | The evolution of animal Argonautes: evidence for the absence of antiviral AGO Argonautes in vertebrates |
title_fullStr | The evolution of animal Argonautes: evidence for the absence of antiviral AGO Argonautes in vertebrates |
title_full_unstemmed | The evolution of animal Argonautes: evidence for the absence of antiviral AGO Argonautes in vertebrates |
title_short | The evolution of animal Argonautes: evidence for the absence of antiviral AGO Argonautes in vertebrates |
title_sort | evolution of animal argonautes: evidence for the absence of antiviral ago argonautes in vertebrates |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5569025/ https://www.ncbi.nlm.nih.gov/pubmed/28835645 http://dx.doi.org/10.1038/s41598-017-08043-5 |
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