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Identification of a Pseudomonas aeruginosa PAO1 DNA Methyltransferase, Its Targets, and Physiological Roles

DNA methylation is widespread among prokaryotes, and most DNA methylation reactions are catalyzed by adenine DNA methyltransferases, which are part of restriction-modification (R-M) systems. R-M systems are known for their role in the defense against foreign DNA; however, DNA methyltransferases also...

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Autores principales: Doberenz, Sebastian, Eckweiler, Denitsa, Reichert, Olga, Jensen, Vanessa, Bunk, Boyke, Spröer, Cathrin, Kordes, Adrian, Frangipani, Emanuela, Luong, Khai, Korlach, Jonas, Heeb, Stephan, Overmann, Jörg, Kaever, Volkhard, Häussler, Susanne
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5358918/
https://www.ncbi.nlm.nih.gov/pubmed/28223461
http://dx.doi.org/10.1128/mBio.02312-16
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author Doberenz, Sebastian
Eckweiler, Denitsa
Reichert, Olga
Jensen, Vanessa
Bunk, Boyke
Spröer, Cathrin
Kordes, Adrian
Frangipani, Emanuela
Luong, Khai
Korlach, Jonas
Heeb, Stephan
Overmann, Jörg
Kaever, Volkhard
Häussler, Susanne
author_facet Doberenz, Sebastian
Eckweiler, Denitsa
Reichert, Olga
Jensen, Vanessa
Bunk, Boyke
Spröer, Cathrin
Kordes, Adrian
Frangipani, Emanuela
Luong, Khai
Korlach, Jonas
Heeb, Stephan
Overmann, Jörg
Kaever, Volkhard
Häussler, Susanne
author_sort Doberenz, Sebastian
collection PubMed
description DNA methylation is widespread among prokaryotes, and most DNA methylation reactions are catalyzed by adenine DNA methyltransferases, which are part of restriction-modification (R-M) systems. R-M systems are known for their role in the defense against foreign DNA; however, DNA methyltransferases also play functional roles in gene regulation. In this study, we used single-molecule real-time (SMRT) sequencing to uncover the genome-wide DNA methylation pattern in the opportunistic pathogen Pseudomonas aeruginosa PAO1. We identified a conserved sequence motif targeted by an adenine methyltransferase of a type I R-M system and quantified the presence of N(6)-methyladenine using liquid chromatography-tandem mass spectrometry (LC-MS/MS). Changes in the PAO1 methylation status were dependent on growth conditions and affected P. aeruginosa pathogenicity in a Galleria mellonella infection model. Furthermore, we found that methylated motifs in promoter regions led to shifts in sense and antisense gene expression, emphasizing the role of enzymatic DNA methylation as an epigenetic control of phenotypic traits in P. aeruginosa. Since the DNA methylation enzymes are not encoded in the core genome, our findings illustrate how the acquisition of accessory genes can shape the global P. aeruginosa transcriptome and thus may facilitate adaptation to new and challenging habitats.
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spelling pubmed-53589182017-03-24 Identification of a Pseudomonas aeruginosa PAO1 DNA Methyltransferase, Its Targets, and Physiological Roles Doberenz, Sebastian Eckweiler, Denitsa Reichert, Olga Jensen, Vanessa Bunk, Boyke Spröer, Cathrin Kordes, Adrian Frangipani, Emanuela Luong, Khai Korlach, Jonas Heeb, Stephan Overmann, Jörg Kaever, Volkhard Häussler, Susanne mBio Research Article DNA methylation is widespread among prokaryotes, and most DNA methylation reactions are catalyzed by adenine DNA methyltransferases, which are part of restriction-modification (R-M) systems. R-M systems are known for their role in the defense against foreign DNA; however, DNA methyltransferases also play functional roles in gene regulation. In this study, we used single-molecule real-time (SMRT) sequencing to uncover the genome-wide DNA methylation pattern in the opportunistic pathogen Pseudomonas aeruginosa PAO1. We identified a conserved sequence motif targeted by an adenine methyltransferase of a type I R-M system and quantified the presence of N(6)-methyladenine using liquid chromatography-tandem mass spectrometry (LC-MS/MS). Changes in the PAO1 methylation status were dependent on growth conditions and affected P. aeruginosa pathogenicity in a Galleria mellonella infection model. Furthermore, we found that methylated motifs in promoter regions led to shifts in sense and antisense gene expression, emphasizing the role of enzymatic DNA methylation as an epigenetic control of phenotypic traits in P. aeruginosa. Since the DNA methylation enzymes are not encoded in the core genome, our findings illustrate how the acquisition of accessory genes can shape the global P. aeruginosa transcriptome and thus may facilitate adaptation to new and challenging habitats. American Society for Microbiology 2017-02-21 /pmc/articles/PMC5358918/ /pubmed/28223461 http://dx.doi.org/10.1128/mBio.02312-16 Text en Copyright © 2017 Doberenz et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (http://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Article
Doberenz, Sebastian
Eckweiler, Denitsa
Reichert, Olga
Jensen, Vanessa
Bunk, Boyke
Spröer, Cathrin
Kordes, Adrian
Frangipani, Emanuela
Luong, Khai
Korlach, Jonas
Heeb, Stephan
Overmann, Jörg
Kaever, Volkhard
Häussler, Susanne
Identification of a Pseudomonas aeruginosa PAO1 DNA Methyltransferase, Its Targets, and Physiological Roles
title Identification of a Pseudomonas aeruginosa PAO1 DNA Methyltransferase, Its Targets, and Physiological Roles
title_full Identification of a Pseudomonas aeruginosa PAO1 DNA Methyltransferase, Its Targets, and Physiological Roles
title_fullStr Identification of a Pseudomonas aeruginosa PAO1 DNA Methyltransferase, Its Targets, and Physiological Roles
title_full_unstemmed Identification of a Pseudomonas aeruginosa PAO1 DNA Methyltransferase, Its Targets, and Physiological Roles
title_short Identification of a Pseudomonas aeruginosa PAO1 DNA Methyltransferase, Its Targets, and Physiological Roles
title_sort identification of a pseudomonas aeruginosa pao1 dna methyltransferase, its targets, and physiological roles
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5358918/
https://www.ncbi.nlm.nih.gov/pubmed/28223461
http://dx.doi.org/10.1128/mBio.02312-16
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