Evidence map›Paper›PMID 24811061›Full record

ArticlePloS one2014

A high-throughput method to examine protein-nucleotide interactions identifies targets of the bacterial transcriptional regulatory protein fur.

Chunxiao Yu, Carlos A Lopez, Han Hu, Yu Xia, David S Freedman, Alexander P Reddington, George G Daaboul, M Selim Unlü, Caroline Attardo Genco

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.7field-weighted citation impact, top 29% 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

3 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Article
  3. 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

9 authors at 1 institution in 1 country.

Chunxiao YuDepartment of Medicine, Section of Infectious Diseases, Boston University School of Medicine, Boston University, Boston, Massachusetts, United States of America.
Carlos A LopezDepartment of Electrical and Computer Engineering, Boston University, Boston, Massachusetts, United States of America.
Han HuBioinformatics Graduate Program, Boston University, Boston, Massachusetts, United States of America.
Yu XiaBioinformatics Graduate Program, Boston University, Boston, Massachusetts, United States of America.
David S FreedmanDepartment of Biomedical Engineering, Boston University, Boston, Massachusetts, United States of America.
Alexander P ReddingtonDepartment of Electrical and Computer Engineering, Boston University, Boston, Massachusetts, United States of America.
George G DaaboulDepartment of Biomedical Engineering, Boston University, Boston, Massachusetts, United States of America.
M Selim UnlüDepartment of Electrical and Computer Engineering, Boston University, Boston, Massachusetts, United States of America; Department of Biomedical Engineering, Boston University, Boston, Massachusetts, United States of America; Physics Department, Boston University, Boston, Massachusetts, United States of America.
Caroline Attardo GencoDepartment of Medicine, Section of Infectious Diseases, Boston University School of Medicine, Boston University, Boston, Massachusetts, United States of America; Department of Microbiology, Boston University School of Medicine, Boston University, Boston, Massachusetts, United States of America.
Boston University · US

Funding

The Gonococcal Fur Regulon: Link to PathogenesisR01AI048611 · NIAID · BOSTON UNIVERSITY MEDICAL CAMPUS · PI GENCO, CAROLINE A · 2001 to 2012
$3.9M
NIAID NIH HHS R01 AI048611NIAID NIH HHS R01AI048611
6 · The paper itself

Abstract

The Ferric uptake regulatory protein (Fur) is a transcriptional regulatory protein that functions to control gene transcription in response to iron in a number of pathogenic bacteria. In this study, we applied a label-free, quantitative and high-throughput analysis method, Interferometric Reflectance Imaging Sensor (IRIS), to rapidly characterize Fur-DNA interactions in vitro with predicted Fur binding sequences in the genome of Neisseria gonorrhoeae, the causative agent of the sexually transmitted disease gonorrhea. IRIS can easily be applied to examine multiple protein-protein, protein-nucleotide and nucleotide-nucleotide complexes simultaneously and demonstrated here that seventy percent of the predicted Fur boxes in promoter regions of iron-induced genes bound to Fur in vitro with a range of affinities as observed using this microarray screening technology. Combining binding data with mRNA expression levels in a gonococcal fur mutant strain allowed us to identify five new gonococcal genes under Fur-mediated direct regulation.

Indexed as

Bacterial ProteinsBase SequenceBiosensing TechniquesConsensus SequenceDNA, BacterialGenome, BacterialNeisseria gonorrhoeaeProtein BindingRegulonRepressor ProteinsSubstrate SpecificityBacterial ProteinsDNA, BacterialRepressor Proteins

Identifiers

PMID24811061
PMCPMC4014563
OpenAlexW2159893527

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.