Evidence map›Paper›PMID 23300489›Full record

ArticlePLoS genetics2013

Comprehensive methylome characterization of Mycoplasma genitalium and Mycoplasma pneumoniae at single-base resolution.

Maria Lluch-Senar, Khai Luong, Verónica Lloréns-Rico, Javier Delgado, Gang Fang, Kristi Spittle, Tyson A Clark, Eric Schadt, Stephen W Turner, Jonas Korlach and 1 more

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 70 papers.

0numbers the graph read from it
0cells of the map it votes in
70citing papers in PubMed
13.2field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

70 citing papers in PubMed, 112 citations in OpenAlex.

  1. Article
  2. Bacterial conjugation in the ruminant pathogenApplied and environmental microbiology · 2025
    Article
  3. Review
  4. Article
  5. Unraveling the adaptive strategies ofFrontiers in cellular and infection microbiology · 2024
    Article
  6. Article
  7. Article
  8. Review
  9. Impacts ofMicrobial genomics · 2022
    Article
  10. Article
  11. Article
  12. Article
  13. Changes in the genomes and methylomes of threeFrontiers in microbiology · 2022
    Article
  14. Frontiers in microbiology · 2022
    Article
  15. Article
  16. Article
  17. Article
  18. ACS synthetic biology · 2020
    Article
  19. NMolecular cell · 2020
    Article
  20. The bacterial epigenome.Nature reviews. Microbiology · 2020
    Review

10 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors at 4 institutions in 2 countries.

Maria Lluch-SenarEMBL/CRG Systems Biology Research Unit, Centre for Genomic Regulation (CRG), Barcelona, Spain. maria.lluch@crg.es
Khai Luong
Verónica Lloréns-Rico
Javier Delgado
Gang Fang
Kristi Spittle
Tyson A Clark
Eric Schadt
Stephen W Turner
Jonas Korlach
Luis Serrano
Pacific Biosciences (United States) · USUniversitat Pompeu Fabra · ESIcahn School of Medicine at Mount Sinai · USInstitució Catalana de Recerca i Estudis Avançats · ES

Funding

SciBay: A New Methodology for Scientific Collaboration and Gene Function DetermiRC2GM092602 · NIGMS · BOSTON UNIVERSITY (CHARLES RIVER CAMPUS) · PI KASIF, SIMON, ROBERTS, RICHARD J · 2009 to 2010
$4.0M
Direct Single Base-Pair Real-Time DNA Methylation SequencingRC2HG005618 · NHGRI · PACIFIC BIOSCIENCES OF CALIFORNIA, INC. · PI TURNER, STEPHEN WHITFIELD · 2009 to 2010
$1.2M
NHGRI NIH HHS 1RC2HG005618-01NHGRI NIH HHS RC2 HG005618NIGMS NIH HHS 1RC2GM092602-01NIGMS NIH HHS RC2 GM092602
6 · The paper itself

Abstract

In the bacterial world, methylation is most commonly associated with restriction-modification systems that provide a defense mechanism against invading foreign genomes. In addition, it is known that methylation plays functionally important roles, including timing of DNA replication, chromosome partitioning, DNA repair, and regulation of gene expression. However, full DNA methylome analyses are scarce due to a lack of a simple methodology for rapid and sensitive detection of common epigenetic marks (ie N(6)-methyladenine (6 mA) and N(4)-methylcytosine (4 mC)), in these organisms. Here, we use Single-Molecule Real-Time (SMRT) sequencing to determine the methylomes of two related human pathogen species, Mycoplasma genitalium G-37 and Mycoplasma pneumoniae M129, with single-base resolution. Our analysis identified two new methylation motifs not previously described in bacteria: a widespread 6 mA methylation motif common to both bacteria (5'-CTAT-3'), as well as a more complex Type I m6A sequence motif in M. pneumoniae (5'-GAN(7)TAY-3'/3'-CTN(7)ATR-5'). We identify the methyltransferase responsible for the common motif and suggest the one involved in M. pneumoniae only. Analysis of the distribution of methylation sites across the genome of M. pneumoniae suggests a potential role for methylation in regulating the cell cycle, as well as in regulation of gene expression. To our knowledge, this is one of the first direct methylome profiling studies with single-base resolution from a bacterial organism.

Indexed as

Mycoplasma genitaliumMycoplasma pneumoniaeDNA MethylationGene Expression Regulation, ArchaealGenome, BacterialHumansMethyltransferasesNucleotide MotifsMethyltransferases

Identifiers

PMID23300489
PMCPMC3536716
OpenAlexW2008951118

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.