Evidence map›Paper›PMID 24272778›Full record

ArticleJournal of bacteriology2014

Genome-scale analyses of Escherichia coli and Salmonella enterica AraC reveal noncanonical targets and an expanded core regulon.

Anne M Stringer, Salvatore Currenti, Richard P Bonocora, Catherine Baranowski, Brianna L Petrone, Michael J Palumbo, Andrew A Reilly, Zhen Zhang, Ivan Erill, Joseph T Wade

Open access · bronzeAbstract read
In one paragraph

Article in Journal of bacteriology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed
4.9field-weighted citation impact, top 5% 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

49 citing papers in PubMed, 78 citations in OpenAlex.

  1. A plasmid-encoded H-NS protein selectively binds its own plasmid.bioRxiv : the preprint server for biology · 2026
    Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Mapping theMicrobiology (Reading, England) · 2024
    Article
  7. Article
  8. Article
  9. Genetic mutation inmSystems · 2024
    Article
  10. Article
  11. Article
  12. Article
  13. Genome-wide mapping of thebioRxiv : the preprint server for biology · 2023
    Article
  14. Article
  15. Review
  16. Development of ONT-cappable-seq to unravel the transcriptional landscape ofComputational and structural biotechnology journal · 2022
    Article
  17. Article
  18. Article
  19. Regulatory roles ofeLife · 2021
    Article
  20. The role of solute binding proteins in signal transduction.Computational and structural biotechnology journal · 2021
    Review
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

10 authors at 4 institutions in 1 country.

Anne M StringerWadsworth Center, New York State Department of Health, Albany, New York, USA.
Salvatore Currenti
Richard P Bonocora
Catherine Baranowski
Brianna L Petrone
Michael J Palumbo
Andrew A Reilly
Zhen Zhang
Ivan Erill
Joseph T Wade
New York State Department of Health · USWadsworth Center · USUniversity at Albany, State University of New York · USUniversity of Maryland, Baltimore County · US

Funding

Pervasive transcription in bacterial genomesDP2OD007188 · OD · WADSWORTH CENTER · PI WADE, JOSEPH THOMAS · 2010 to 2010
$2.4M
NIH HHS 1DP2OD007188NIH HHS DP2 OD007188
6 · The paper itself

Abstract

Escherichia coli AraC is a well-described transcription activator of genes involved in arabinose metabolism. Using complementary genomic approaches, chromatin immunoprecipitation (ChIP)-chip, and transcription profiling, we identify direct regulatory targets of AraC, including five novel target genes: ytfQ, ydeN, ydeM, ygeA, and polB. Strikingly, only ytfQ has an established connection to arabinose metabolism, suggesting that AraC has a broader function than previously described. We demonstrate arabinose-dependent repression of ydeNM by AraC, in contrast to the well-described arabinose-dependent activation of other target genes. We also demonstrate unexpected read-through of transcription at the Rho-independent terminators downstream of araD and araE, leading to significant increases in the expression of polB and ygeA, respectively. AraC is highly conserved in the related species Salmonella enterica. We use ChIP sequencing (ChIP-seq) and RNA sequencing (RNA-seq) to map the AraC regulon in S. enterica. A comparison of the E. coli and S. enterica AraC regulons, coupled with a bioinformatic analysis of other related species, reveals a conserved regulatory network across the family Enterobacteriaceae comprised of 10 genes associated with arabinose transport and metabolism.

Indexed as

ArabinoseAraC Transcription FactorBase SequenceBinding SitesChromosome MappingDNA, BacterialDNA-Directed RNA PolymerasesEscherichia coliEscherichia coli ProteinsGene Expression Regulation, BacterialGenome, BacterialRegulonSalmonella entericaArabinoseAraC protein, E coliAraC Transcription FactorDNA, BacterialDNA-Directed RNA PolymerasesEscherichia coli Proteins

Identifiers

PMID24272778
PMCPMC3911152
OpenAlexW2021541861

What OpenQuestion holds

Textmetadata
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.