Evidence map›Paper›PMID 26020636›Full record

ArticlePLoS genetics2015

In Vitro Whole Genome DNA Binding Analysis of the Bacterial Replication Initiator and Transcription Factor DnaA.

Janet L Smith, Alan D Grossman

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
–field-weighted citation impact, top 95% 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

24 citing papers in PubMed, 0 citations in OpenAlex.

  1. A rapid test for protein-DNA interactions.Nucleic acids research · 2026
    Article
  2. Article
  3. Review
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  6. Review
  7. Article
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  10. Article
  11. Article
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  14. Article
  15. Genes and Proteins Involved inAntimicrobial agents and chemotherapy · 2018
    Article
  16. Article
  17. Phosphorylation of theFrontiers in microbiology · 2018
    Article
  18. Structure and Function of theFrontiers in microbiology · 2018
    Article
  19. Article
  20. 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

2 authors at 1 institution in 1 country.

Janet L SmithDepartment of Biology, Massachusetts Institute of Technology, Cambridge, Massachusetts, United States of America.
Alan D GrossmanDepartment of Biology, Massachusetts Institute of Technology, Cambridge, Massachusetts, United States of America.
Massachusetts Institute of Technology · US

Funding

Cell Cycle and Sporulation in Bacillis SubtillisR37GM041934 · NIGMS · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI GROSSMAN, ALAN D · 2009 to 2017
$4.8M
INITITATION OF SPORULATION IN BACILLUS SUBTILISR01GM041934 · NIGMS · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI GROSSMAN, ALAN D · 1989 to 2007
$2.6M
NIGMS NIH HHS GM41934NIGMS NIH HHS R01 GM041934NIGMS NIH HHS R37 GM041934
6 · The paper itself

Abstract

DnaA, the replication initiation protein in bacteria, is an AAA+ ATPase that binds and hydrolyzes ATP and exists in a heterogeneous population of ATP-DnaA and ADP-DnaA. DnaA binds cooperatively to the origin of replication and several other chromosomal regions, and functions as a transcription factor at some of these regions. We determined the binding properties of Bacillus subtilis DnaA to genomic DNA in vitro at single nucleotide resolution using in vitro DNA affinity purification and deep sequencing (IDAP-Seq). We used these data to identify 269 binding regions, refine the consensus sequence of the DnaA binding site, and compare the relative affinity of binding regions for ATP-DnaA and ADP-DnaA. Most sites had a slightly higher affinity for ATP-DnaA than ADP-DnaA, but a few had a strong preference for binding ATP-DnaA. Of the 269 sites, only the eight strongest binding ones have been observed to bind DnaA in vivo, suggesting that other cellular factors or the amount of available DnaA in vivo restricts DnaA binding to these additional sites. Conversely, we found several chromosomal regions that were bound by DnaA in vivo but not in vitro, and that the nucleoid-associated protein Rok was required for binding in vivo. Our in vitro characterization of the inherent ability of DnaA to bind the genome at single nucleotide resolution provides a backdrop for interpreting data on in vivo binding and regulation of DnaA, and is an approach that should be adaptable to many other DNA binding proteins.

Indexed as

Genome, BacterialAdenosine TriphosphatasesAdenosine TriphosphateBacillus subtilisBacterial ProteinsBinding SitesDNADNA-Binding ProteinsDNA ReplicationNucleotidesProtein BindingAdenosine TriphosphatasesAdenosine TriphosphateBacterial ProteinsDNADnaA protein, BacteriaDNA-Binding ProteinsNucleotides

Identifiers

PMID26020636
PMCPMC4447404
OpenAlexW1984256397

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.