Evidence map›Paper›PMID 23630319›Full record

ArticleNucleic acids research2013

A bistable hysteretic switch in an activator-repressor regulated restriction-modification system.

Kristen Williams, Michael A Savageau, Robert M Blumenthal

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

19 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Low-level expression of the Type II restriction-modification system confers potent bacteriophage resistance in Escherichia coli.DNA research : an international journal for rapid publication of reports on genes and genomes · 2020
    Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Review
  17. Article
  18. Molecular mechanisms of multiple toxin-antitoxin systems are coordinated to govern the persister phenotype.Proceedings of the National Academy of Sciences of the United States of America · 2013
    Article
  19. Phenotypic deconstruction of gene circuitry.Chaos (Woodbury, N.Y.) · 2013
    Article
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

3 authors at 1 institution in 1 country.

Kristen WilliamsDepartment of Medical Microbiology & Immunology, and Program in Bioinformatics, University of Toledo, Toledo, OH 43614, USA.
Michael A Savageau
Robert M Blumenthal
University of California, Davis · US

Funding

GENE CIRCUITS AND BIOCHEMICAL NETWORKSR01GM030054 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI SAVAGEAU, MICHAEL A · 1985 to 2015
$3.2M
NIGMS NIH HHS GM030054-27NIGMS NIH HHS R01 GM030054
6 · The paper itself

Abstract

Restriction-modification (RM) systems are extremely widespread among bacteria and archaea, and are often specified by mobile genetic elements. In type II RM systems, where the restriction endonuclease (REase) and protective DNA methyltransferase (MTase) are separate proteins, a major regulatory challenge is delaying expression of the REase relative to the MTase after RM genes enter a new host cell. Basic understanding of this regulation is available for few RM systems, and detailed understanding for none. The PvuII RM system is one of a large subset in which the central regulatory role is played by an activator-repressor protein (called C, for controller). REase expression depends upon activation by C, whereas expression of the MTase does not. Thus delay of REase expression depends on the rate of C-protein accumulation. This is a nonlinear process, as C also activates transcription of its own gene. Mathematical modeling of the PvuII system led to the unexpected predictions of responsiveness to a factor not previously studied in RM system control--gene copy number--and of a hysteretic response. In this study, those predictions have been confirmed experimentally. The results may apply to many other C-regulated RM systems, and help explain their ability to spread so widely.

Indexed as

Gene DosageGene Expression Regulation, BacterialBacterial ProteinsBase SequenceDeoxyribonucleases, Type II Site-SpecificDNA-Cytosine MethylasesKineticsModels, GeneticMolecular Sequence DataRepressor ProteinsTrans-ActivatorsTranscription FactorsBacterial ProteinsCAGCTG-specific type II deoxyribonucleasesDeoxyribonucleases, Type II Site-SpecificDNA-Cytosine MethylasesDNA modification methylase PvuIIRepressor ProteinsTrans-ActivatorsTranscription Factors

Identifiers

PMID23630319
PMCPMC3695507
OpenAlexW2101402161

What OpenQuestion holds

Textmetadata
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.