Evidence map›Paper›PMID 25648898›Full record

ArticleThe Journal of biological chemistry2015

Upstream binding of idling RNA polymerase modulates transcription initiation from a nearby promoter.

Veneta Gerganova, Sebastian Maurer, Liubov Stoliar, Aleksandre Japaridze, Giovanni Dietler, William Nasser, Tamara Kutateladze, Andrew Travers, Georgi Muskhelishvili

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2015. 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
2.2field-weighted citation impact, top 12% 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, 20 citations in OpenAlex.

  1. Article
  2. Article
  3. Biophysical reviews · 2023
    Review
  4. IHF and Fis asInternational journal of molecular sciences · 2023
    Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. 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

9 authors at 2 institutions in 2 countries.

Veneta GerganovaFrom the School of Engineering and Science, Jacobs University Bremen, Campus Ring 1, D-28759 Bremen, Germany.
Sebastian MaurerFrom the School of Engineering and Science, Jacobs University Bremen, Campus Ring 1, D-28759 Bremen, Germany.
Liubov StoliarFrom the School of Engineering and Science, Jacobs University Bremen, Campus Ring 1, D-28759 Bremen, Germany.
Aleksandre Japaridzethe Laboratory of the Physics of Living Matter, EPFL, CH-1015 Lausanne, Switzerland.
Giovanni Dietlerthe Laboratory of the Physics of Living Matter, EPFL, CH-1015 Lausanne, Switzerland.
William Nasserthe UMR5240 CNRS/INSA/UCB, Université de Lyon, F-69003, INSA-Lyon, Villeurbanne, F-69621, France.
Tamara Kutateladzethe Ivane Beritashvili Centre of Experimental Biomedicine, Gotua str.14, Tbilisi, Georgia, and.
Andrew Traversthe MRC Laboratory of Molecular Biology, Hills Road, Cambridge CB2 QH, United Kingdom.
Georgi MuskhelishviliFrom the School of Engineering and Science, Jacobs University Bremen, Campus Ring 1, D-28759 Bremen, Germany, g.muskhelishvili@jacobs-university.de.
École Polytechnique Fédérale de Lausanne · CHMRC Laboratory of Molecular Biology · GB

Funding

Medical Research Council MC_U105178783
6 · The paper itself

Abstract

The bacterial gene regulatory regions often demonstrate distinctly organized arrays of RNA polymerase binding sites of ill-defined function. Previously we observed a module of closely spaced polymerase binding sites upstream of the canonical promoter of the Escherichia coli fis operon. FIS is an abundant nucleoid-associated protein involved in adjusting the chromosomal DNA topology to changing cellular physiology. Here we show that simultaneous binding of the polymerase at the canonical fis promoter and an upstream transcriptionally inactive site stabilizes a RNAP oligomeric complex in vitro. We further show that modulation of the upstream binding of RNA polymerase affects the fis promoter activity both in vivo and in vitro. The effect of the upstream RNA polymerase binding on the fis promoter activity depends on the spatial arrangement of polymerase binding sites and DNA supercoiling. Our data suggest that a specific DNA geometry of the nucleoprotein complex stabilized on concomitant binding of RNA polymerase molecules at the fis promoter and the upstream region acts as a topological device regulating the fis transcription. We propose that transcriptionally inactive RNA polymerase molecules can act as accessory factors regulating the transcription initiation from a nearby promoter.

Indexed as

Promoter Regions, GeneticTranscription Initiation, GeneticDNA, BacterialDNA-Directed RNA PolymerasesDNA, SuperhelicalEscherichia coliEscherichia coli ProteinsFactor For Inversion Stimulation ProteinGene Expression Regulation, BacterialMicroscopy, Atomic ForceProtein BindingDNA, BacterialDNA-Directed RNA PolymerasesDNA, SuperhelicalEscherichia coli ProteinsFactor For Inversion Stimulation ProteinFis protein, E coliAtomic Force Microscopy (AFM)Bacterial TranscriptionDNA TopologyEscherichia coli (E. coli)fisRNA PolymeraseTranscription Promoter

Identifiers

PMID25648898
PMCPMC4375467
OpenAlexW1997035038

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.