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The complex methylome of the human gastric pathogen Helicobacter pylori

The genome of Helicobacter pylori is remarkable for its large number of restriction-modification (R-M) systems, and strain-specific diversity in R-M systems has been suggested to limit natural transformation, the major driving force of genetic diversification in H. pylori. We have determined the com...

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Autores principales: Krebes, Juliane, Morgan, Richard D., Bunk, Boyke, Spröer, Cathrin, Luong, Khai, Parusel, Raphael, Anton, Brian P., König, Christoph, Josenhans, Christine, Overmann, Jörg, Roberts, Richard J., Korlach, Jonas, Suerbaum, Sebastian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3936762/
https://www.ncbi.nlm.nih.gov/pubmed/24302578
http://dx.doi.org/10.1093/nar/gkt1201
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author Krebes, Juliane
Morgan, Richard D.
Bunk, Boyke
Spröer, Cathrin
Luong, Khai
Parusel, Raphael
Anton, Brian P.
König, Christoph
Josenhans, Christine
Overmann, Jörg
Roberts, Richard J.
Korlach, Jonas
Suerbaum, Sebastian
author_facet Krebes, Juliane
Morgan, Richard D.
Bunk, Boyke
Spröer, Cathrin
Luong, Khai
Parusel, Raphael
Anton, Brian P.
König, Christoph
Josenhans, Christine
Overmann, Jörg
Roberts, Richard J.
Korlach, Jonas
Suerbaum, Sebastian
author_sort Krebes, Juliane
collection PubMed
description The genome of Helicobacter pylori is remarkable for its large number of restriction-modification (R-M) systems, and strain-specific diversity in R-M systems has been suggested to limit natural transformation, the major driving force of genetic diversification in H. pylori. We have determined the comprehensive methylomes of two H. pylori strains at single base resolution, using Single Molecule Real-Time (SMRT®) sequencing. For strains 26695 and J99-R3, 17 and 22 methylated sequence motifs were identified, respectively. For most motifs, almost all sites occurring in the genome were detected as methylated. Twelve novel methylation patterns corresponding to nine recognition sequences were detected (26695, 3; J99-R3, 6). Functional inactivation, correction of frameshifts as well as cloning and expression of candidate methyltransferases (MTases) permitted not only the functional characterization of multiple, yet undescribed, MTases, but also revealed novel features of both Type I and Type II R-M systems, including frameshift-mediated changes of sequence specificity and the interaction of one MTase with two alternative specificity subunits resulting in different methylation patterns. The methylomes of these well-characterized H. pylori strains will provide a valuable resource for future studies investigating the role of H. pylori R-M systems in limiting transformation as well as in gene regulation and host interaction.
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spelling pubmed-39367622014-03-04 The complex methylome of the human gastric pathogen Helicobacter pylori Krebes, Juliane Morgan, Richard D. Bunk, Boyke Spröer, Cathrin Luong, Khai Parusel, Raphael Anton, Brian P. König, Christoph Josenhans, Christine Overmann, Jörg Roberts, Richard J. Korlach, Jonas Suerbaum, Sebastian Nucleic Acids Res Genomics The genome of Helicobacter pylori is remarkable for its large number of restriction-modification (R-M) systems, and strain-specific diversity in R-M systems has been suggested to limit natural transformation, the major driving force of genetic diversification in H. pylori. We have determined the comprehensive methylomes of two H. pylori strains at single base resolution, using Single Molecule Real-Time (SMRT®) sequencing. For strains 26695 and J99-R3, 17 and 22 methylated sequence motifs were identified, respectively. For most motifs, almost all sites occurring in the genome were detected as methylated. Twelve novel methylation patterns corresponding to nine recognition sequences were detected (26695, 3; J99-R3, 6). Functional inactivation, correction of frameshifts as well as cloning and expression of candidate methyltransferases (MTases) permitted not only the functional characterization of multiple, yet undescribed, MTases, but also revealed novel features of both Type I and Type II R-M systems, including frameshift-mediated changes of sequence specificity and the interaction of one MTase with two alternative specificity subunits resulting in different methylation patterns. The methylomes of these well-characterized H. pylori strains will provide a valuable resource for future studies investigating the role of H. pylori R-M systems in limiting transformation as well as in gene regulation and host interaction. Oxford University Press 2014-02 2013-12-02 /pmc/articles/PMC3936762/ /pubmed/24302578 http://dx.doi.org/10.1093/nar/gkt1201 Text en © The Author(s) 2013. Published by Oxford University Press. http://creativecommons.org/licenses/by/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Genomics
Krebes, Juliane
Morgan, Richard D.
Bunk, Boyke
Spröer, Cathrin
Luong, Khai
Parusel, Raphael
Anton, Brian P.
König, Christoph
Josenhans, Christine
Overmann, Jörg
Roberts, Richard J.
Korlach, Jonas
Suerbaum, Sebastian
The complex methylome of the human gastric pathogen Helicobacter pylori
title The complex methylome of the human gastric pathogen Helicobacter pylori
title_full The complex methylome of the human gastric pathogen Helicobacter pylori
title_fullStr The complex methylome of the human gastric pathogen Helicobacter pylori
title_full_unstemmed The complex methylome of the human gastric pathogen Helicobacter pylori
title_short The complex methylome of the human gastric pathogen Helicobacter pylori
title_sort complex methylome of the human gastric pathogen helicobacter pylori
topic Genomics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3936762/
https://www.ncbi.nlm.nih.gov/pubmed/24302578
http://dx.doi.org/10.1093/nar/gkt1201
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