Evidence map›Paper›PMID 10698953›Full record

ArticleThe EMBO journal2000

Escherichia coli promoter opening and -10 recognition: mutational analysis of sigma70.

M S Fenton, S J Lee, J D Gralla

Abstract read
In one paragraph

Article in The EMBO journal, 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 57 papers.

0numbers the graph read from it
0cells of the map it votes in
57citing 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

57 citing papers in PubMed.

  1. Article
  2. Article
  3. Systematic dissection of σCell reports · 2021
    Article
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  9. Review
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  11. Review
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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.

M S FentonDepartment of Chemistry, University of California, Los Angeles, PO Box 951569, Los Angeles, CA 90095-1569, USA.
S J Lee
J D Gralla

Funding

MECHANISMS OF REPRESSION IN BACTERIAR01GM035754 · NIGMS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI GRALLA, JAY D · 1986 to 2006
$2.0M
NIGMS NIH HHS GM35754NIGMS NIH HHS R01 GM035754
6 · The paper itself

Abstract

The opening of specific segments of DNA is required for most types of genetic readout, including sigma70-dependent transcription. To learn how this occurs, a series of single point mutations were introduced into sigma70 region 2. These were assayed for duplex DNA binding, DNA opening and DNA double strand-single strand fork junction binding. Band shift assays for closed complex formation implicated a series of arginine and aromatic residues within a minimal 26 amino acid region. Permanganate assays implicated two additional aromatic residues in DNA opening, known to form a parallel stack of the type that can accept a flipped-out base. Substitution for either of these aromatics had no effect on duplex probe recognition. However, when a single unpaired -11 nucleotide is added to the probe, the mutants fail to bind appropriately to give heparin resistance. A model for DNA opening is presented in which duplex recognition by regions 2.3, 2.4 and 2.5 of sigma positions the pair of aromatic amino acids, which then create the fork junction required for stable opening.

Indexed as

Bacterial ProteinsBase SequenceDNA, BacterialDNA-Binding ProteinsDNA-Directed RNA PolymerasesDNA Mutational AnalysisEscherichia coliGene Expression Regulation, BacterialMolecular Sequence DataPromoter Regions, GeneticSigma FactorBacterial ProteinsDNA, BacterialDNA-Binding ProteinsDNA-Directed RNA PolymerasesRNA polymerase sigma 70Sigma Factor

Identifiers

PMID10698953
PMCPMC305651

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.