Evidence map›Paper›PMID 28067866›Full record

ArticleNature microbiology2017

Horizontally acquired AT-rich genes in Escherichia coli cause toxicity by sequestering RNA polymerase.

Lisa E Lamberte, Gabriele Baniulyte, Shivani S Singh, Anne M Stringer, Richard P Bonocora, Mathew Stracy, Achillefs N Kapanidis, Joseph T Wade, David C Grainger

Open access · greenAbstract read
In one paragraph

Article in Nature microbiology, 2017. 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
8.4field-weighted citation impact, top 2% 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

57 citing papers in PubMed, 89 citations in OpenAlex.

  1. A plasmid-encoded H-NS protein selectively binds its own plasmid.bioRxiv : the preprint server for biology · 2026
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  10. H-NS controls the susceptibility ofFrontiers in veterinary science · 2025
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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

9 authors at 4 institutions in 2 countries.

Lisa E LamberteInstitute of Microbiology and Infection, School of Biosciences, University of Birmingham, Birmingham B15 2TT, UK.
Gabriele BaniulyteInstitute of Microbiology and Infection, School of Biosciences, University of Birmingham, Birmingham B15 2TT, UK.
Shivani S SinghInstitute of Microbiology and Infection, School of Biosciences, University of Birmingham, Birmingham B15 2TT, UK.
Anne M StringerNew York State Department of Health, Wadsworth Center, Albany, New York 12208, USA.
Richard P BonocoraNew York State Department of Health, Wadsworth Center, Albany, New York 12208, USA.
Mathew StracyBiological Physics Research Group, Clarendon Laboratory, Department of Physics, University of Oxford, Oxford OX1 3PU, UK.
Achillefs N KapanidisBiological Physics Research Group, Clarendon Laboratory, Department of Physics, University of Oxford, Oxford OX1 3PU, UK.
Joseph T WadeNew York State Department of Health, Wadsworth Center, Albany, New York 12208, USA.
David C GraingerInstitute of Microbiology and Infection, School of Biosciences, University of Birmingham, Birmingham B15 2TT, UK.
University of Birmingham · GBUniversity of Oxford · GBWadsworth Center · USUniversity at Albany, State University of New York · US

Funding

Pervasive transcription in bacterial genomesDP2OD007188 · OD · WADSWORTH CENTER · PI WADE, JOSEPH THOMAS · 2010 to 2010
$2.4M
Biotechnology and Biological Sciences Research Council BB/H01795X/1NIH HHS DP2 OD007188Wellcome Trust 085092Wellcome Trust 110164Wellcome Trust 204684Wellcome Trust 204684/Z/16/Z
6 · The paper itself

Abstract

Horizontal gene transfer permits rapid dissemination of genetic elements between individuals in bacterial populations. Transmitted DNA sequences may encode favourable traits. However, if the acquired DNA has an atypical base composition, it can reduce host fitness. Consequently, bacteria have evolved strategies to minimize the harmful effects of foreign genes. Most notably, xenogeneic silencing proteins bind incoming DNA that has a higher AT content than the host genome. An enduring question has been why such sequences are deleterious. Here, we showed that the toxicity of AT-rich DNA in Escherichia coli frequently results from constitutive transcription initiation within the coding regions of genes. Left unchecked, this causes titration of RNA polymerase and a global downshift in host gene expression. Accordingly, a mutation in RNA polymerase that diminished the impact of AT-rich DNA on host fitness reduced transcription from constitutive, but not activator-dependent, promoters.

Indexed as

Gene Transfer, HorizontalAT Rich SequenceBase CompositionDNA, BacterialDNA-Binding ProteinsDNA-Directed RNA PolymerasesEscherichia coliEscherichia coli ProteinsFimbriae ProteinsGene Expression Regulation, BacterialGenes, BacterialGene SilencingGenetic FitnessGenomeMutationPromoter Regions, GeneticDNA, BacterialDNA-Binding ProteinsDNA-Directed RNA PolymerasesEscherichia coli ProteinsFimbriae ProteinsFimG protein, E coli

Identifiers

PMID28067866
PMCPMC7610989
OpenAlexW2568345024

What OpenQuestion holds

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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.