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Evidence for an evolutionary antagonism between Mrr and Type III modification systems
The Mrr protein of Escherichia coli is a laterally acquired Type IV restriction endonuclease with specificity for methylated DNA. While Mrr nuclease activity can be elicited by high-pressure stress in E. coli MG1655, its (over)expression per se does not confer any obvious toxicity. In this study, ho...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3152355/ https://www.ncbi.nlm.nih.gov/pubmed/21504983 http://dx.doi.org/10.1093/nar/gkr219 |
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author | Tesfazgi Mebrhatu, Mehari Wywial, Ewa Ghosh, Anirban Michiels, Chris W. Lindner, Ariel B. Taddei, François Bujnicki, Janusz M. Van Melderen, Laurence Aertsen, Abram |
author_facet | Tesfazgi Mebrhatu, Mehari Wywial, Ewa Ghosh, Anirban Michiels, Chris W. Lindner, Ariel B. Taddei, François Bujnicki, Janusz M. Van Melderen, Laurence Aertsen, Abram |
author_sort | Tesfazgi Mebrhatu, Mehari |
collection | PubMed |
description | The Mrr protein of Escherichia coli is a laterally acquired Type IV restriction endonuclease with specificity for methylated DNA. While Mrr nuclease activity can be elicited by high-pressure stress in E. coli MG1655, its (over)expression per se does not confer any obvious toxicity. In this study, however, we discovered that Mrr of E. coli MG1655 causes distinct genotoxicity when expressed in Salmonella typhimurium LT2. Genetic screening enabled us to contribute this toxicity entirely to the presence of the endogenous Type III restriction modification system (StyLTI) of S. typhimurium LT2. The StyLTI system consists of the Mod DNA methyltransferase and the Res restriction endonuclease, and we revealed that expression of the LT2 mod gene was sufficient to trigger Mrr activity in E. coli MG1655. Moreover, we could demonstrate that horizontal acquisition of the MG1655 mrr locus can drive the loss of endogenous Mod functionality present in S. typhimurium LT2 and E. coli ED1a, and observed a strong anti-correlation between close homologues of MG1655 mrr and LT2 mod in the genome database. This apparent evolutionary antagonism is further discussed in the light of a possible role for Mrr as defense mechanism against the establishment of epigenetic regulation by foreign DNA methyltransferases. |
format | Online Article Text |
id | pubmed-3152355 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-31523552011-08-08 Evidence for an evolutionary antagonism between Mrr and Type III modification systems Tesfazgi Mebrhatu, Mehari Wywial, Ewa Ghosh, Anirban Michiels, Chris W. Lindner, Ariel B. Taddei, François Bujnicki, Janusz M. Van Melderen, Laurence Aertsen, Abram Nucleic Acids Res Genome Integrity, Repair and Replication The Mrr protein of Escherichia coli is a laterally acquired Type IV restriction endonuclease with specificity for methylated DNA. While Mrr nuclease activity can be elicited by high-pressure stress in E. coli MG1655, its (over)expression per se does not confer any obvious toxicity. In this study, however, we discovered that Mrr of E. coli MG1655 causes distinct genotoxicity when expressed in Salmonella typhimurium LT2. Genetic screening enabled us to contribute this toxicity entirely to the presence of the endogenous Type III restriction modification system (StyLTI) of S. typhimurium LT2. The StyLTI system consists of the Mod DNA methyltransferase and the Res restriction endonuclease, and we revealed that expression of the LT2 mod gene was sufficient to trigger Mrr activity in E. coli MG1655. Moreover, we could demonstrate that horizontal acquisition of the MG1655 mrr locus can drive the loss of endogenous Mod functionality present in S. typhimurium LT2 and E. coli ED1a, and observed a strong anti-correlation between close homologues of MG1655 mrr and LT2 mod in the genome database. This apparent evolutionary antagonism is further discussed in the light of a possible role for Mrr as defense mechanism against the establishment of epigenetic regulation by foreign DNA methyltransferases. Oxford University Press 2011-08 2011-04-19 /pmc/articles/PMC3152355/ /pubmed/21504983 http://dx.doi.org/10.1093/nar/gkr219 Text en © The Author(s) 2011. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/2.5 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.5), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Genome Integrity, Repair and Replication Tesfazgi Mebrhatu, Mehari Wywial, Ewa Ghosh, Anirban Michiels, Chris W. Lindner, Ariel B. Taddei, François Bujnicki, Janusz M. Van Melderen, Laurence Aertsen, Abram Evidence for an evolutionary antagonism between Mrr and Type III modification systems |
title | Evidence for an evolutionary antagonism between Mrr and Type III modification systems |
title_full | Evidence for an evolutionary antagonism between Mrr and Type III modification systems |
title_fullStr | Evidence for an evolutionary antagonism between Mrr and Type III modification systems |
title_full_unstemmed | Evidence for an evolutionary antagonism between Mrr and Type III modification systems |
title_short | Evidence for an evolutionary antagonism between Mrr and Type III modification systems |
title_sort | evidence for an evolutionary antagonism between mrr and type iii modification systems |
topic | Genome Integrity, Repair and Replication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3152355/ https://www.ncbi.nlm.nih.gov/pubmed/21504983 http://dx.doi.org/10.1093/nar/gkr219 |
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