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Exploration of DNA processing features unravels novel properties of ICE conjugation in Gram-positive bacteria
Integrative and conjugative elements (ICEs) are important drivers of horizontal gene transfer in prokaryotes. They are responsible for antimicrobial resistance spread, a major current health concern. ICEs are initially processed by relaxases that recognize the binding site of oriT sequence and nick...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9371924/ https://www.ncbi.nlm.nih.gov/pubmed/35849337 http://dx.doi.org/10.1093/nar/gkac607 |
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author | Laroussi, Haifa Aoudache, Yanis Robert, Emilie Libante, Virginie Thiriet, Louise Mias-Lucquin, Dominique Douzi, Badreddine Roussel, Yvonne Chauvot de Beauchêne, Isaure Soler, Nicolas Leblond-Bourget, Nathalie |
author_facet | Laroussi, Haifa Aoudache, Yanis Robert, Emilie Libante, Virginie Thiriet, Louise Mias-Lucquin, Dominique Douzi, Badreddine Roussel, Yvonne Chauvot de Beauchêne, Isaure Soler, Nicolas Leblond-Bourget, Nathalie |
author_sort | Laroussi, Haifa |
collection | PubMed |
description | Integrative and conjugative elements (ICEs) are important drivers of horizontal gene transfer in prokaryotes. They are responsible for antimicrobial resistance spread, a major current health concern. ICEs are initially processed by relaxases that recognize the binding site of oriT sequence and nick at a conserved nic site. The ICESt3/Tn916/ICEBs1 superfamily, which is widespread among Firmicutes, encodes uncanonical relaxases belonging to a recently identified family called MOB(T). This family is related to the rolling circle replication initiators of the Rep_trans family. The nic site of these MOB(T) relaxases is conserved but their DNA binding site is still unknown. Here, we identified the bind site of RelSt3, the MOB(T) relaxase from ICESt3. Unexpectedly, we found this bind site distantly located from the nic site. We revealed that the binding of the RelSt3 N-terminal HTH domain is required for efficient nicking activity. We also deciphered the role of RelSt3 in the initial and final stages of DNA processing during conjugation. Especially, we demonstrated a strand transfer activity, and the formation of covalent DNA-relaxase intermediate for a MOB(T) relaxase. |
format | Online Article Text |
id | pubmed-9371924 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-93719242022-08-12 Exploration of DNA processing features unravels novel properties of ICE conjugation in Gram-positive bacteria Laroussi, Haifa Aoudache, Yanis Robert, Emilie Libante, Virginie Thiriet, Louise Mias-Lucquin, Dominique Douzi, Badreddine Roussel, Yvonne Chauvot de Beauchêne, Isaure Soler, Nicolas Leblond-Bourget, Nathalie Nucleic Acids Res Nucleic Acid Enzymes Integrative and conjugative elements (ICEs) are important drivers of horizontal gene transfer in prokaryotes. They are responsible for antimicrobial resistance spread, a major current health concern. ICEs are initially processed by relaxases that recognize the binding site of oriT sequence and nick at a conserved nic site. The ICESt3/Tn916/ICEBs1 superfamily, which is widespread among Firmicutes, encodes uncanonical relaxases belonging to a recently identified family called MOB(T). This family is related to the rolling circle replication initiators of the Rep_trans family. The nic site of these MOB(T) relaxases is conserved but their DNA binding site is still unknown. Here, we identified the bind site of RelSt3, the MOB(T) relaxase from ICESt3. Unexpectedly, we found this bind site distantly located from the nic site. We revealed that the binding of the RelSt3 N-terminal HTH domain is required for efficient nicking activity. We also deciphered the role of RelSt3 in the initial and final stages of DNA processing during conjugation. Especially, we demonstrated a strand transfer activity, and the formation of covalent DNA-relaxase intermediate for a MOB(T) relaxase. Oxford University Press 2022-07-18 /pmc/articles/PMC9371924/ /pubmed/35849337 http://dx.doi.org/10.1093/nar/gkac607 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of Nucleic Acids Research. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Nucleic Acid Enzymes Laroussi, Haifa Aoudache, Yanis Robert, Emilie Libante, Virginie Thiriet, Louise Mias-Lucquin, Dominique Douzi, Badreddine Roussel, Yvonne Chauvot de Beauchêne, Isaure Soler, Nicolas Leblond-Bourget, Nathalie Exploration of DNA processing features unravels novel properties of ICE conjugation in Gram-positive bacteria |
title | Exploration of DNA processing features unravels novel properties of ICE conjugation in Gram-positive bacteria |
title_full | Exploration of DNA processing features unravels novel properties of ICE conjugation in Gram-positive bacteria |
title_fullStr | Exploration of DNA processing features unravels novel properties of ICE conjugation in Gram-positive bacteria |
title_full_unstemmed | Exploration of DNA processing features unravels novel properties of ICE conjugation in Gram-positive bacteria |
title_short | Exploration of DNA processing features unravels novel properties of ICE conjugation in Gram-positive bacteria |
title_sort | exploration of dna processing features unravels novel properties of ice conjugation in gram-positive bacteria |
topic | Nucleic Acid Enzymes |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9371924/ https://www.ncbi.nlm.nih.gov/pubmed/35849337 http://dx.doi.org/10.1093/nar/gkac607 |
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