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ArdA proteins from different mobile genetic elements can bind to the EcoKI Type I DNA methyltransferase of E. coli K12()
Anti-restriction and anti-modification (anti-RM) is the ability to prevent cleavage by DNA restriction–modification (RM) systems of foreign DNA entering a new bacterial host. The evolutionary consequence of anti-RM is the enhanced dissemination of mobile genetic elements. Homologues of ArdA anti-RM...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier Pub. Co
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3969726/ https://www.ncbi.nlm.nih.gov/pubmed/24368349 http://dx.doi.org/10.1016/j.bbapap.2013.12.008 |
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author | Chen, Kai Reuter, Marcel Sanghvi, Bansi Roberts, Gareth A. Cooper, Laurie P. Tilling, Matthew Blakely, Garry W. Dryden, David T.F. |
author_facet | Chen, Kai Reuter, Marcel Sanghvi, Bansi Roberts, Gareth A. Cooper, Laurie P. Tilling, Matthew Blakely, Garry W. Dryden, David T.F. |
author_sort | Chen, Kai |
collection | PubMed |
description | Anti-restriction and anti-modification (anti-RM) is the ability to prevent cleavage by DNA restriction–modification (RM) systems of foreign DNA entering a new bacterial host. The evolutionary consequence of anti-RM is the enhanced dissemination of mobile genetic elements. Homologues of ArdA anti-RM proteins are encoded by genes present in many mobile genetic elements such as conjugative plasmids and transposons within bacterial genomes. The ArdA proteins cause anti-RM by mimicking the DNA structure bound by Type I RM enzymes. We have investigated ArdA proteins from the genomes of Enterococcus faecalis V583, Staphylococcus aureus Mu50 and Bacteroides fragilis NCTC 9343, and compared them to the ArdA protein expressed by the conjugative transposon Tn916. We find that despite having very different structural stability and secondary structure content, they can all bind to the EcoKI methyltransferase, a core component of the EcoKI Type I RM system. This finding indicates that the less structured ArdA proteins become fully folded upon binding. The ability of ArdA from diverse mobile elements to inhibit Type I RM systems from other bacteria suggests that they are an advantage for transfer not only between closely-related bacteria but also between more distantly related bacterial species. |
format | Online Article Text |
id | pubmed-3969726 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Elsevier Pub. Co |
record_format | MEDLINE/PubMed |
spelling | pubmed-39697262014-03-31 ArdA proteins from different mobile genetic elements can bind to the EcoKI Type I DNA methyltransferase of E. coli K12() Chen, Kai Reuter, Marcel Sanghvi, Bansi Roberts, Gareth A. Cooper, Laurie P. Tilling, Matthew Blakely, Garry W. Dryden, David T.F. Biochim Biophys Acta Article Anti-restriction and anti-modification (anti-RM) is the ability to prevent cleavage by DNA restriction–modification (RM) systems of foreign DNA entering a new bacterial host. The evolutionary consequence of anti-RM is the enhanced dissemination of mobile genetic elements. Homologues of ArdA anti-RM proteins are encoded by genes present in many mobile genetic elements such as conjugative plasmids and transposons within bacterial genomes. The ArdA proteins cause anti-RM by mimicking the DNA structure bound by Type I RM enzymes. We have investigated ArdA proteins from the genomes of Enterococcus faecalis V583, Staphylococcus aureus Mu50 and Bacteroides fragilis NCTC 9343, and compared them to the ArdA protein expressed by the conjugative transposon Tn916. We find that despite having very different structural stability and secondary structure content, they can all bind to the EcoKI methyltransferase, a core component of the EcoKI Type I RM system. This finding indicates that the less structured ArdA proteins become fully folded upon binding. The ability of ArdA from diverse mobile elements to inhibit Type I RM systems from other bacteria suggests that they are an advantage for transfer not only between closely-related bacteria but also between more distantly related bacterial species. Elsevier Pub. Co 2014-03 /pmc/articles/PMC3969726/ /pubmed/24368349 http://dx.doi.org/10.1016/j.bbapap.2013.12.008 Text en © 2013 The Authors http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Article Chen, Kai Reuter, Marcel Sanghvi, Bansi Roberts, Gareth A. Cooper, Laurie P. Tilling, Matthew Blakely, Garry W. Dryden, David T.F. ArdA proteins from different mobile genetic elements can bind to the EcoKI Type I DNA methyltransferase of E. coli K12() |
title | ArdA proteins from different mobile genetic elements can bind to the EcoKI Type I DNA methyltransferase of E. coli K12() |
title_full | ArdA proteins from different mobile genetic elements can bind to the EcoKI Type I DNA methyltransferase of E. coli K12() |
title_fullStr | ArdA proteins from different mobile genetic elements can bind to the EcoKI Type I DNA methyltransferase of E. coli K12() |
title_full_unstemmed | ArdA proteins from different mobile genetic elements can bind to the EcoKI Type I DNA methyltransferase of E. coli K12() |
title_short | ArdA proteins from different mobile genetic elements can bind to the EcoKI Type I DNA methyltransferase of E. coli K12() |
title_sort | arda proteins from different mobile genetic elements can bind to the ecoki type i dna methyltransferase of e. coli k12() |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3969726/ https://www.ncbi.nlm.nih.gov/pubmed/24368349 http://dx.doi.org/10.1016/j.bbapap.2013.12.008 |
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