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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...
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/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. |
format | Online Article Text |
id | pubmed-3936762 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
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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