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      The Epigenomic Landscape of Prokaryotes

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          Abstract

          DNA methylation acts in concert with restriction enzymes to protect the integrity of prokaryotic genomes. Studies in a limited number of organisms suggest that methylation also contributes to prokaryotic genome regulation, but the prevalence and properties of such non-restriction-associated methylation systems remain poorly understood. Here, we used single molecule, real-time sequencing to map DNA modifications including m6A, m4C, and m5C across the genomes of 230 diverse bacterial and archaeal species. We observed DNA methylation in nearly all (93%) organisms examined, and identified a total of 834 distinct reproducibly methylated motifs. This data enabled annotation of the DNA binding specificities of 620 DNA Methyltransferases (MTases), doubling known specificities for previously hard to study Type I, IIG and III MTases, and revealing their extraordinary diversity. Strikingly, 48% of organisms harbor active Type II MTases with no apparent cognate restriction enzyme. These active ‘orphan’ MTases are present in diverse bacterial and archaeal phyla and show motif specificities and methylation patterns consistent with functions in gene regulation and DNA replication. Our results reveal the pervasive presence of DNA methylation throughout the prokaryotic kingdoms, as well as the diversity of sequence specificities and potential functions of DNA methylation systems.

          Author Summary

          DNA methylation is a chemical modification of DNA present in many prokaryotic genomes. The best-known role of DNA methylation is as a component of restriction-modification systems. In these systems, restriction enzymes target foreign DNA for cleavage, while DNA methylation protects the host genome from destruction. Studies in a handful of organisms show that DNA methylation may also act independently of restriction systems and function in genome regulation. However, a lack of technologies has limited the study of DNA methylation to a small number of organisms, and the broader patterns and functions of DNA methylation remain unknown. Here we use SMRT-sequencing to determine the genome wide DNA methylation patterns of more than 200 diverse bacteria and archaea. We show that DNA methylation is pervasive and present in more than 90% of studied organisms. Analysis of this data enabled annotation of the specific DNA binding sites of more than 600 restriction systems, revealing their extraordinary diversity. Strikingly, we observed widespread DNA methylation in the absence of restriction systems. Analyses of these patterns reveal that they are conserved through evolution, and likely function in genome regulation. Thus DNA methylation may play a far wider function in prokaryotic genome biology than was previously supposed.

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          Most cited references36

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          A nomenclature for restriction enzymes, DNA methyltransferases, homing endonucleases and their genes.

          R Roberts (2003)
          A nomenclature is described for restriction endonucleases, DNA methyltransferases, homing endonucleases and related genes and gene products. It provides explicit categories for the many different Type II enzymes now identified and provides a system for naming the putative genes found by sequence analysis of microbial genomes.
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            Mismatch repair in replication fidelity, genetic recombination, and cancer biology.

            Mismatch repair stabilizes the cellular genome by correcting DNA replication errors and by blocking recombination events between divergent DNA sequences. The reaction responsible for strand-specific correction of mispaired bases has been highly conserved during evolution, and homologs of bacterial MutS and MutL, which play key roles in mismatch recognition and initiation of repair, have been identified in yeast and mammalian cells. Inactivation of genes encoding these activities results in a large increase in spontaneous mutability, and in the case of mice and men, predisposition to tumor development.
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              N6-methyl-adenine: an epigenetic signal for DNA-protein interactions.

              N(6)-methyl-adenine is found in the genomes of bacteria, archaea, protists and fungi. Most bacterial DNA adenine methyltransferases are part of restriction-modification systems. Certain groups of Proteobacteria also harbour solitary DNA adenine methyltransferases that provide signals for DNA-protein interactions. In gamma-proteobacteria, Dam methylation regulates chromosome replication, nucleoid segregation, DNA repair, transposition of insertion elements and transcription of specific genes. In Salmonella, Haemophilus, Yersinia and Vibrio species and in pathogenic Escherichia coli, Dam methylation is required for virulence. In alpha-proteobacteria, CcrM methylation regulates the cell cycle in Caulobacter, Rhizobium and Agrobacterium, and has a role in Brucella abortus infection.
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                Author and article information

                Contributors
                Role: Editor
                Journal
                PLoS Genet
                PLoS Genet
                plos
                plosgen
                PLoS Genetics
                Public Library of Science (San Francisco, CA USA )
                1553-7390
                1553-7404
                12 February 2016
                February 2016
                : 12
                : 2
                : e1005854
                Affiliations
                [1 ]Genomics Division, Lawrence Berkeley National Laboratory, Berkeley, California, United States of America
                [2 ]U.S. Department of Energy Joint Genome Institute, Walnut Creek, California, United States of America
                [3 ]Pacific Biosciences, Menlo Park, California, United States of America
                [4 ]Physical Biosciences Division, Lawrence Berkeley National Laboratory, Berkeley, California, United States of America
                [5 ]New England Biolabs, Ipswich, Massachusetts, United States of America
                University of Minnesota, UNITED STATES
                Author notes

                RJR, RDM, JP and AF are employees of New England Biolabs (NEB), a company that sells DNA methylases and restriction enzymes. NEB paid for a part of the research. JK and TAC are full-time employees at Pacific Biosciences, a company commercializing single molecule, real-time sequencing technologies.

                Conceived and designed the experiments: MJB RRM EMR JK LAP RJR. Performed the experiments: CGD RDM KS ZZ. Analyzed the data: MJB TAC AF RF JF DDK RDM JP RJR. Contributed reagents/materials/analysis tools: AMD KW. Wrote the paper: MJB AV RDM RJR.

                Article
                PGENETICS-D-15-02290
                10.1371/journal.pgen.1005854
                4752239
                26870957
                5af5e5fb-567f-48ee-8525-dbbb28ea43bd

                This is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 public domain dedication.

                History
                : 15 September 2015
                : 19 January 2016
                Page count
                Figures: 6, Tables: 2, Pages: 28
                Funding
                RJR and AF were supported by the Small Business Innovation Research Program (National Institute of General Medical Sciences) of the National Institutes of Health award number R44GM105125 to RJR. Research was conducted at the E.O. Lawrence Berkeley National Laboratory and performed under Department of Energy Contract DE-AC02-05CH11231, University of California. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
                Categories
                Research Article
                Biology and Life Sciences
                Molecular Biology
                Molecular Biology Techniques
                Sequencing Techniques
                Sequence Analysis
                Sequence Motif Analysis
                Research and Analysis Methods
                Molecular Biology Techniques
                Sequencing Techniques
                Sequence Analysis
                Sequence Motif Analysis
                Biology and life sciences
                Cell biology
                Chromosome biology
                Chromatin
                Chromatin modification
                DNA methylation
                Biology and life sciences
                Genetics
                Epigenetics
                Chromatin
                Chromatin modification
                DNA methylation
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                Genetics
                Gene expression
                Chromatin
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                DNA
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                Biochemistry
                Nucleic acids
                DNA
                DNA modification
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                Biology and life sciences
                Genetics
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                Gene expression
                DNA modification
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                Gene Expression
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                Research and Analysis Methods
                Database and Informatics Methods
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                Genetics
                Genomics
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                Cell Biology
                Cellular Types
                Prokaryotic Cells
                Biology and Life Sciences
                Computational Biology
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                DNA
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                Biology and life sciences
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                Custom metadata
                Data files have been deposited in GEO under accession numbers GSE69872.

                Genetics
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