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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
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.
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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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