Evidence map›Paper›PMID 26675057›Full record

ArticleScientific reports2015

Predicting the impact of promoter variability on regulatory outputs.

Naomi N Kreamer, Rob Phillips, Dianne K Newman, James Q Boedicker

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.0field-weighted citation impact, top 19% 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

8 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Transcriptional Regulators Controlling Virulence inInternational journal of molecular sciences · 2023
    Review
  5. Article
  6. Article
  7. Article
  8. 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

4 authors at 2 institutions in 1 country.

Naomi N KreamerDivision of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA 91125, USA.
Rob PhillipsDivision of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA 91125, USA.
Dianne K NewmanDivision of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA 91125, USA.
James Q BoedickerDepartment of Physics and Astronomy, University of Southern California, Los Angeles, CA 90089, USA.
California Institute of Technology · USUniversity of Southern California · US

Funding

TRANS-NETWORK PROJECTSU54CA143869 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI KOPP, PETER ANDREAS · 2009 to 2013
$12.8M
NIH Director's Pioneer Award (RMI)DP1OD000217 · OD · CALIFORNIA INSTITUTE OF TECHNOLOGY · PI PHILLIPS, ROB · 2004 to 2008
$4.0M
Single-Molecule and Single-Cell Analysis of Transcription Factor-DNA ComplexesR01GM085286 · NIGMS · CALIFORNIA INSTITUTE OF TECHNOLOGY · PI PHILLIPS, ROB · 2009 to 2015
$2.8M
Geobiological approaches to understanding pulmonary infections in situR01HL117328 · NHLBI · CALIFORNIA INSTITUTE OF TECHNOLOGY · PI NEWMAN, DIANNE K · 2012 to 2016
$2.1M
Howard Hughes Medical InstituteNCI NIH HHS 1 U54 CA143869NCI NIH HHS U54 CA143869NHLBI NIH HHS 5R01HL117328-03NHLBI NIH HHS R01 HL117328NIGMS NIH HHS R01 GM085286NIGMS NIH HHS R01 GM085286BNIH HHS DP1 OD000217
6 · The paper itself

Abstract

The increased availability of whole genome sequences calls for quantitative models of global gene expression, yet predicting gene expression patterns directly from genome sequence remains a challenge. We examine the contributions of an individual regulator, the ferrous iron-responsive regulatory element, BqsR, on global patterns of gene expression in Pseudomonas aeruginosa. The position weight matrix (PWM) derived for BqsR uncovered hundreds of likely binding sites throughout the genome. Only a subset of these potential binding sites had a regulatory consequence, suggesting that BqsR/DNA interactions were not captured within the PWM or that the broader regulatory context at each promoter played a greater role in setting promoter outputs. The architecture of the BqsR operator was systematically varied to understand how binding site parameters influence expression. We found that BqsR operator affinity was predicted by the PWM well. At many promoters the surrounding regulatory context, including overlapping operators of BqsR or the presence of RhlR binding sites, were influential in setting promoter outputs. These results indicate more comprehensive models that include local regulatory contexts are needed to develop a predictive understanding of global regulatory outputs.

Indexed as

Gene Expression Regulation, BacterialAlgorithmsBacterial ProteinsBase SequenceBinding SitesDNA, BacterialFerrous CompoundsGene Expression ProfilingGenome, BacterialModels, GeneticPromoter Regions, GeneticProtein BindingPseudomonas aeruginosaRegulatory Sequences, Nucleic AcidBacterial ProteinsDNA, BacterialFerrous Compounds

Identifiers

PMID26675057
PMCPMC4682146
OpenAlexW2221429303

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.