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The interplay of restriction-modification systems with mobile genetic elements and their prokaryotic hosts
The roles of restriction-modification (R-M) systems in providing immunity against horizontal gene transfer (HGT) and in stabilizing mobile genetic elements (MGEs) have been much debated. However, few studies have precisely addressed the distribution of these systems in light of HGT, its mechanisms a...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4176335/ https://www.ncbi.nlm.nih.gov/pubmed/25120263 http://dx.doi.org/10.1093/nar/gku734 |
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author | Oliveira, Pedro H. Touchon, Marie Rocha, Eduardo P.C. |
author_facet | Oliveira, Pedro H. Touchon, Marie Rocha, Eduardo P.C. |
author_sort | Oliveira, Pedro H. |
collection | PubMed |
description | The roles of restriction-modification (R-M) systems in providing immunity against horizontal gene transfer (HGT) and in stabilizing mobile genetic elements (MGEs) have been much debated. However, few studies have precisely addressed the distribution of these systems in light of HGT, its mechanisms and its vectors. We analyzed the distribution of R-M systems in 2261 prokaryote genomes and found their frequency to be strongly dependent on the presence of MGEs, CRISPR-Cas systems, integrons and natural transformation. Yet R-M systems are rare in plasmids, in prophages and nearly absent from other phages. Their abundance depends on genome size for small genomes where it relates with HGT but saturates at two occurrences per genome. Chromosomal R-M systems might evolve under cycles of purifying and relaxed selection, where sequence conservation depends on the biochemical activity and complexity of the system and total gene loss is frequent. Surprisingly, analysis of 43 pan-genomes suggests that solitary R-M genes rarely arise from the degradation of R-M systems. Solitary genes are transferred by large MGEs, whereas complete systems are more frequently transferred autonomously or in small MGEs. Our results suggest means of testing the roles for R-M systems and their associations with MGEs. |
format | Online Article Text |
id | pubmed-4176335 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-41763352014-12-01 The interplay of restriction-modification systems with mobile genetic elements and their prokaryotic hosts Oliveira, Pedro H. Touchon, Marie Rocha, Eduardo P.C. Nucleic Acids Res Nucleic Acid Enzymes The roles of restriction-modification (R-M) systems in providing immunity against horizontal gene transfer (HGT) and in stabilizing mobile genetic elements (MGEs) have been much debated. However, few studies have precisely addressed the distribution of these systems in light of HGT, its mechanisms and its vectors. We analyzed the distribution of R-M systems in 2261 prokaryote genomes and found their frequency to be strongly dependent on the presence of MGEs, CRISPR-Cas systems, integrons and natural transformation. Yet R-M systems are rare in plasmids, in prophages and nearly absent from other phages. Their abundance depends on genome size for small genomes where it relates with HGT but saturates at two occurrences per genome. Chromosomal R-M systems might evolve under cycles of purifying and relaxed selection, where sequence conservation depends on the biochemical activity and complexity of the system and total gene loss is frequent. Surprisingly, analysis of 43 pan-genomes suggests that solitary R-M genes rarely arise from the degradation of R-M systems. Solitary genes are transferred by large MGEs, whereas complete systems are more frequently transferred autonomously or in small MGEs. Our results suggest means of testing the roles for R-M systems and their associations with MGEs. Oxford University Press 2014-09-15 2014-08-12 /pmc/articles/PMC4176335/ /pubmed/25120263 http://dx.doi.org/10.1093/nar/gku734 Text en © The Author(s) 2014. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://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 Oliveira, Pedro H. Touchon, Marie Rocha, Eduardo P.C. The interplay of restriction-modification systems with mobile genetic elements and their prokaryotic hosts |
title | The interplay of restriction-modification systems with mobile genetic elements and their prokaryotic hosts |
title_full | The interplay of restriction-modification systems with mobile genetic elements and their prokaryotic hosts |
title_fullStr | The interplay of restriction-modification systems with mobile genetic elements and their prokaryotic hosts |
title_full_unstemmed | The interplay of restriction-modification systems with mobile genetic elements and their prokaryotic hosts |
title_short | The interplay of restriction-modification systems with mobile genetic elements and their prokaryotic hosts |
title_sort | interplay of restriction-modification systems with mobile genetic elements and their prokaryotic hosts |
topic | Nucleic Acid Enzymes |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4176335/ https://www.ncbi.nlm.nih.gov/pubmed/25120263 http://dx.doi.org/10.1093/nar/gku734 |
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