Evidence map›Paper›PMID 22114557›Full record

ArticlePLoS pathogens2011

Indirect DNA readout by an H-NS related protein: structure of the DNA complex of the C-terminal domain of Ler.

Tiago N Cordeiro, Holger Schmidt, Cristina Madrid, Antonio Juárez, Pau Bernadó, Christian Griesinger, Jesús García, Miquel Pons

Open access · goldAbstract read
In one paragraph

Article in PLoS pathogens, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing 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

36 citing papers in PubMed, 61 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Review
  6. Deciphering Sequence-Specific DNA Binding by H-NS Using Molecular Simulation.Methods in molecular biology (Clifton, N.J.) · 2024
    Article
  7. Article
  8. One Earth: The Equilibrium between the Human and the Bacterial Worlds.International journal of molecular sciences · 2023
    Review
  9. ToxR activates theProceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  10. Article
  11. Article
  12. PchE Regulation ofInternational journal of molecular sciences · 2020
    Article
  13. Transcription of Bacterial Chromatin.Journal of molecular biology · 2019
    Review
  14. Article
  15. Article
  16. Article
  17. Review
  18. Charged residues in the H-NS linker drive DNA binding and gene silencing in single cells.Proceedings of the National Academy of Sciences of the United States of America · 2017
    Article
  19. Article
  20. 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

8 authors at 3 institutions in 2 countries.

Tiago N CordeiroInstitute for Research in Biomedicine (IRB Barcelona), Parc Científic de Barcelona, Barcelona, Spain.
Holger Schmidt
Cristina Madrid
Antonio Juárez
Pau Bernadó
Christian Griesinger
Jesús García
Miquel Pons
Institute for Research in Biomedicine · ESUniversitat de Barcelona · ESMax Planck Institute for Biophysical Chemistry · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ler, a member of the H-NS protein family, is the master regulator of the LEE pathogenicity island in virulent Escherichia coli strains. Here, we determined the structure of a complex between the DNA-binding domain of Ler (CT-Ler) and a 15-mer DNA duplex. CT-Ler recognizes a preexisting structural pattern in the DNA minor groove formed by two consecutive regions which are narrower and wider, respectively, compared with standard B-DNA. The compressed region, associated with an AT-tract, is sensed by the side chain of Arg90, whose mutation abolishes the capacity of Ler to bind DNA. The expanded groove allows the approach of the loop in which Arg90 is located. This is the first report of an experimental structure of a DNA complex that includes a protein belonging to the H-NS family. The indirect readout mechanism not only explains the capacity of H-NS and other H-NS family members to modulate the expression of a large number of genes but also the origin of the specificity displayed by Ler. Our results point to a general mechanism by which horizontally acquired genes may be specifically recognized by members of the H-NS family.

Indexed as

ArginineDNA, B-FormDNA-Binding ProteinsEscherichia coliEscherichia coli ProteinsFimbriae ProteinsGene Transfer, HorizontalGenomic IslandsProtein Structure, TertiaryTrans-ActivatorsArginineDNA, B-FormDNA-Binding ProteinsEscherichia coli ProteinsFimbriae ProteinsFimG protein, E coliLer protein, E coliTrans-Activators

Identifiers

PMID22114557
PMCPMC3219716
OpenAlexW2092948899

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Registered trials

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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.