Evidence map›Paper›PMID 24589779›Full record

ArticleGenes & development2014

Structural basis for promoter specificity switching of RNA polymerase by a phage factor.

Shunsuke Tagami, Shun-ichi Sekine, Leonid Minakhin, Daria Esyunina, Ryogo Akasaka, Mikako Shirouzu, Andrey Kulbachinskiy, Konstantin Severinov, Shigeyuki Yokoyama

Open access · diamondAbstract read
In one paragraph

Article in Genes & development, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
–field-weighted citation impact
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

18 citing papers in PubMed, 34 citations in OpenAlex.

  1. Article
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  12. Base excision repair of oxidative DNA damage: from mechanism to disease.Frontiers in bioscience (Landmark edition) · 2017
    Review
  13. Review
  14. Distinct pathways of RNA polymerase regulation by a phage-encoded factor.Proceedings of the National Academy of Sciences of the United States of America · 2015
    Article
  15. Article
  16. Article
  17. Article
  18. 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 6 institutions in 4 countries.

Shunsuke TagamiRIKEN Systems and Structural Biology Center, Tsurumi-ku, Yokohama 230-0045, Japan;
Shun-ichi Sekine
Leonid Minakhin
Daria Esyunina
Ryogo Akasaka
Mikako Shirouzu
Andrey Kulbachinskiy
Konstantin Severinov
Shigeyuki Yokoyama
Systems Biology Institute · JPCE Technologies (United Kingdom) · GBEnvironmental and Occupational Health Sciences Institute · USInstitute of Molecular Genetics · RUPeter the Great St. Petersburg Polytechnic University · RURussian Academy of Sciences · RU

Funding

PHS HHS R01 59295PHS HHS R21 A1074769
6 · The paper itself

Abstract

Transcription of DNA to RNA by DNA-dependent RNA polymerase (RNAP) is the first step of gene expression and a major regulation point. Bacteriophages hijack their host's transcription machinery and direct it to serve their needs. The gp39 protein encoded by Thermus thermophilus phage P23-45 binds the host's RNAP and inhibits transcription initiation from its major "-10/-35" class promoters. Phage promoters belonging to the minor "extended -10" class are minimally inhibited. We report the crystal structure of the T. thermophilus RNAP holoenzyme complexed with gp39, which explains the mechanism for RNAP promoter specificity switching. gp39 simultaneously binds to the RNAP β-flap domain and the C-terminal domain of the σ subunit (region 4 of the σ subunit [σ4]), thus relocating the β-flap tip and σ4. The ~45 Å displacement of σ4 is incompatible with its binding to the -35 promoter consensus element, thus accounting for the inhibition of transcription from -10/-35 class promoters. In contrast, this conformational change is compatible with the recognition of extended -10 class promoters. These results provide the structural bases for the conformational modulation of the host's RNAP promoter specificity to switch gene expression toward supporting phage development for gp39 and, potentially, other phage proteins, such as T4 AsiA.

Indexed as

Models, MolecularThermus thermophilusBacteriophagesDNA-Directed RNA PolymerasesGene Expression Regulation, ViralHoloenzymesPromoter Regions, GeneticProtein BindingProtein Structure, QuaternarySubstrate SpecificityViral ProteinsDNA-Directed RNA PolymerasesHoloenzymesViral ProteinsbacteriophageRNA polymerasetranscription controltranscription factorX-ray crystallography

Identifiers

PMID24589779
PMCPMC3950348
OpenAlexW2126335425

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.