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Pervasive Suicidal Integrases in Deep-Sea Archaea
Mobile genetic elements (MGEs) often encode integrases which catalyze the site-specific insertion of their genetic information into the host genome and the reverse reaction of excision. Hyperthermophilic archaea harbor integrases belonging to the SSV-family which carry the MGE recombination site wit...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7253208/ https://www.ncbi.nlm.nih.gov/pubmed/32068866 http://dx.doi.org/10.1093/molbev/msaa041 |
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author | Badel, Catherine Da Cunha, Violette Forterre, Patrick Oberto, Jacques |
author_facet | Badel, Catherine Da Cunha, Violette Forterre, Patrick Oberto, Jacques |
author_sort | Badel, Catherine |
collection | PubMed |
description | Mobile genetic elements (MGEs) often encode integrases which catalyze the site-specific insertion of their genetic information into the host genome and the reverse reaction of excision. Hyperthermophilic archaea harbor integrases belonging to the SSV-family which carry the MGE recombination site within their open reading frame. Upon integration into the host genome, SSV integrases disrupt their own gene into two inactive pseudogenes and are termed suicidal for this reason. The evolutionary maintenance of suicidal integrases, concurring with the high prevalence and multiples recruitments of these recombinases by archaeal MGEs, is highly paradoxical. To elucidate this phenomenon, we analyzed the wide phylogenomic distribution of a prominent class of suicidal integrases which revealed a highly variable integration site specificity. Our results highlighted the remarkable hybrid nature of these enzymes encoded from the assembly of inactive pseudogenes of different origins. The characterization of the biological properties of one of these integrases, Int(pT26-2) showed that this enzyme was active over a wide range of temperatures up to 99 °C and displayed a less-stringent site specificity requirement than comparable integrases. These observations concurred in explaining the pervasiveness of these suicidal integrases in the most hyperthermophilic organisms. The biochemical and phylogenomic data presented here revealed a target site switching system operating on highly thermostable integrases and suggested a new model for split gene reconstitution. By generating fast-evolving pseudogenes at high frequency, suicidal integrases constitute a powerful model to approach the molecular mechanisms involved in the generation of active genes variants by the recombination of proto-genes. |
format | Online Article Text |
id | pubmed-7253208 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-72532082020-06-02 Pervasive Suicidal Integrases in Deep-Sea Archaea Badel, Catherine Da Cunha, Violette Forterre, Patrick Oberto, Jacques Mol Biol Evol Discoveries Mobile genetic elements (MGEs) often encode integrases which catalyze the site-specific insertion of their genetic information into the host genome and the reverse reaction of excision. Hyperthermophilic archaea harbor integrases belonging to the SSV-family which carry the MGE recombination site within their open reading frame. Upon integration into the host genome, SSV integrases disrupt their own gene into two inactive pseudogenes and are termed suicidal for this reason. The evolutionary maintenance of suicidal integrases, concurring with the high prevalence and multiples recruitments of these recombinases by archaeal MGEs, is highly paradoxical. To elucidate this phenomenon, we analyzed the wide phylogenomic distribution of a prominent class of suicidal integrases which revealed a highly variable integration site specificity. Our results highlighted the remarkable hybrid nature of these enzymes encoded from the assembly of inactive pseudogenes of different origins. The characterization of the biological properties of one of these integrases, Int(pT26-2) showed that this enzyme was active over a wide range of temperatures up to 99 °C and displayed a less-stringent site specificity requirement than comparable integrases. These observations concurred in explaining the pervasiveness of these suicidal integrases in the most hyperthermophilic organisms. The biochemical and phylogenomic data presented here revealed a target site switching system operating on highly thermostable integrases and suggested a new model for split gene reconstitution. By generating fast-evolving pseudogenes at high frequency, suicidal integrases constitute a powerful model to approach the molecular mechanisms involved in the generation of active genes variants by the recombination of proto-genes. Oxford University Press 2020-06 2020-02-18 /pmc/articles/PMC7253208/ /pubmed/32068866 http://dx.doi.org/10.1093/molbev/msaa041 Text en © The Author(s) 2020. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Discoveries Badel, Catherine Da Cunha, Violette Forterre, Patrick Oberto, Jacques Pervasive Suicidal Integrases in Deep-Sea Archaea |
title | Pervasive Suicidal Integrases in Deep-Sea Archaea |
title_full | Pervasive Suicidal Integrases in Deep-Sea Archaea |
title_fullStr | Pervasive Suicidal Integrases in Deep-Sea Archaea |
title_full_unstemmed | Pervasive Suicidal Integrases in Deep-Sea Archaea |
title_short | Pervasive Suicidal Integrases in Deep-Sea Archaea |
title_sort | pervasive suicidal integrases in deep-sea archaea |
topic | Discoveries |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7253208/ https://www.ncbi.nlm.nih.gov/pubmed/32068866 http://dx.doi.org/10.1093/molbev/msaa041 |
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