Evidence map›Paper›PMID 37978176›Full record

ArticleNature communications2023

The environmentally-regulated interplay between local three-dimensional chromatin organisation and transcription of proVWX in E. coli.

Fatema-Zahra M Rashid, Frédéric G E Crémazy, Andreas Hofmann, David Forrest, David C Grainger, Dieter W Heermann, Remus T Dame

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
9.1field-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

16 citing papers in PubMed, 29 citations in OpenAlex.

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  16. Expanding the genetic toolbox for the obligate human pathogenFrontiers in bioengineering and biotechnology · 2024
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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

7 authors at 3 institutions in 4 countries.

Fatema-Zahra M RashidMacromolecular Biochemistry, Leiden Institute of Chemistry, Leiden University, Leiden, 2333CC, The Netherlands.ORCID 0000-0003-2023-9046
Frédéric G E CrémazyMacromolecular Biochemistry, Leiden Institute of Chemistry, Leiden University, Leiden, 2333CC, The Netherlands.ORCID 0000-0002-9375-1588
Andreas HofmannStatistical Physics and Theoretical Biophysics, Heidelberg University, Heidelberg, D-69120, Germany.ORCID 0000-0002-4800-8429
David ForrestSchool of Biosciences, University of Birmingham, Edgbaston, B15 2TT, UK.ORCID 0000-0003-4740-7134
David C GraingerSchool of Biosciences, University of Birmingham, Edgbaston, B15 2TT, UK.ORCID 0000-0003-3375-5154
Dieter W HeermannStatistical Physics and Theoretical Biophysics, Heidelberg University, Heidelberg, D-69120, Germany.ORCID 0000-0002-3148-8382
Remus T DameMacromolecular Biochemistry, Leiden Institute of Chemistry, Leiden University, Leiden, 2333CC, The Netherlands. rtdame@chem.leidenuniv.nl.ORCID 0000-0001-9863-1692
Leiden University · NLHeidelberg University · DEUniversity of Birmingham · GB

Funding

Human Frontier Science Program (HFSP) RGP0014/2014Nederlandse Organisatie voor Wetenschappelijk Onderzoek (Netherlands Organisation for Scientific Research) OCENW.GROOT.2019.012Wellcome Trust 212193/Z/18/Z
6 · The paper itself

Abstract

Nucleoid associated proteins (NAPs) maintain the architecture of bacterial chromosomes and regulate gene expression. Thus, their role as transcription factors may involve three-dimensional chromosome re-organisation. While this model is supported by in vitro studies, direct in vivo evidence is lacking. Here, we use RT-qPCR and 3C-qPCR to study the transcriptional and architectural profiles of the H-NS (histone-like nucleoid structuring protein)-regulated, osmoresponsive proVWX operon of Escherichia coli at different osmolarities and provide in vivo evidence for transcription regulation by NAP-mediated chromosome re-modelling in bacteria. By consolidating our in vivo investigations with earlier in vitro and in silico studies that provide mechanistic details of how H-NS re-models DNA in response to osmolarity, we report that activation of proVWX in response to a hyperosmotic shock involves the destabilization of H-NS-mediated bridges anchored between the proVWX downstream and upstream regulatory elements (DRE and URE), and between the DRE and ygaY that lies immediately downstream of proVWX. The re-establishment of these bridges upon adaptation to hyperosmolarity represses the operon. Our results also reveal additional structural features associated with changes in proVWX transcript levels such as the decompaction of local chromatin upstream of the operon, highlighting that further complexity underlies the regulation of this model operon. H-NS and H-NS-like proteins are wide-spread amongst bacteria, suggesting that chromosome re-modelling may be a typical feature of transcriptional control in bacteria.

Indexed as

Escherichia coliEscherichia coli ProteinsBacterial ProteinsChromatinDNA-Binding ProteinsGene Expression Regulation, BacterialOperonTranscription FactorsTranscription, GeneticBacterial ProteinsChromatinDNA-Binding ProteinsEscherichia coli ProteinsTranscription Factors

Identifiers

PMID37978176
PMCPMC10656529
OpenAlexW4388750722

What OpenQuestion holds

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LicenceCC BY
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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.