Evidence map›Paper›PMID 19181705›Full record

ArticleNucleic acids research2009

DNA sampling: a method for probing protein binding at specific loci on bacterial chromosomes.

Matej Butala, Stephen J W Busby, David J Lee

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
3.3field-weighted citation impact, top 8% 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

14 citing papers in PubMed, 33 citations in OpenAlex.

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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 2 institutions in 2 countries.

Matej ButalaSchool of Biosciences, University of Birmingham, Birmingham B15 2TT, UK.
Stephen J W Busby
David J Lee
University of Birmingham · GBUniversity of Ljubljana · SI

Funding

Biotechnology and Biological Sciences Research Council BB/C501484/1Wellcome Trust
6 · The paper itself

Abstract

We describe a protocol, DNA sampling, for the rapid isolation of specific segments of DNA, together with bound proteins, from Escherichia coli K-12. The DNA to be sampled is generated as a discrete fragment within cells by the yeast I-SceI meganuclease, and is purified using FLAG-tagged LacI repressor and beads carrying anti-FLAG antibody. We illustrate the method by investigating the proteins bound to the colicin K gene regulatory region, either before or after induction of the colicin K gene promoter.

Indexed as

Bacterial ProteinsChromosomes, BacterialColicinsDNA, BacterialDNA-Binding ProteinsElectrophoresis, Polyacrylamide GelEndodeoxyribonucleasesEscherichia coli K12Escherichia coli ProteinsGenetic TechniquesLac RepressorsMass SpectrometryPromoter Regions, GeneticRepressor ProteinsBacterial ProteinsColicinsDNA, BacterialDNA-Binding ProteinsEndodeoxyribonucleasesEscherichia coli ProteinsLacI protein, E coliLac RepressorsRepressor Proteins

Identifiers

PMID19181705
PMCPMC2655658
OpenAlexW2019808128

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.