Evidence map›Paper›PMID 26070674›Full record

ArticleApplied and environmental microbiology2015

Silencing of Essential Genes within a Highly Coordinated Operon in Escherichia coli.

Shan Goh, Angela Hohmeier, Timothy C Stone, Victoria Offord, Francisco Sarabia, Cristina Garcia-Ruiz, Liam Good

Open access · bronzeAbstract read
In one paragraph

Article in Applied and environmental microbiology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.0field-weighted citation impact, top 21% 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

4 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
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 2 institutions in 2 countries.

Shan GohDepartment of Pathology and Pathogen Biology, The Royal Veterinary College, Hatfield, United Kingdom sgoh@rvc.ac.uk.
Angela HohmeierDepartment of Pathology and Pathogen Biology, The Royal Veterinary College, Hatfield, United Kingdom.
Timothy C StoneDepartment of Pathology and Pathogen Biology, The Royal Veterinary College, Hatfield, United Kingdom Central Biotechnology Services and Institute of Translation, Innovation, Methodology and Engagement, School of Medicine, Heath Park, Cardiff University, Cardiff, United Kingdom Institute of Psychological Medicine and Clinical Neurosciences, School of Medicine, Cardiff University, Cardiff, United Kingdom.
Victoria OffordDepartment of Pathology and Pathogen Biology, The Royal Veterinary College, Hatfield, United Kingdom.
Francisco SarabiaDepartment of Organic Chemistry, Faculty of Sciences, University of Malaga, Malaga, Spain.
Cristina Garcia-RuizDepartment of Organic Chemistry, Faculty of Sciences, University of Malaga, Malaga, Spain.
Liam GoodDepartment of Pathology and Pathogen Biology, The Royal Veterinary College, Hatfield, United Kingdom.
Royal Veterinary College · GBUniversidad de Málaga · ES

Funding

Wellcome Trust
6 · The paper itself

Abstract

Essential bacterial genes located within operons are particularly challenging to study independently because of coordinated gene expression and the nonviability of knockout mutants. Essentiality scores for many operon genes remain uncertain. Antisense RNA (asRNA) silencing or in-frame gene disruption of genes may help establish essentiality but can lead to polar effects on genes downstream or upstream of the target gene. Here, the Escherichia coli ribF-ileS-lspA-fkpB-ispH operon was used to evaluate the possibility of independently studying an essential gene using expressed asRNA and target gene overexpression to deregulate coupled expression. The gene requirement for growth in conditional silencing strains was determined by the relationship of target mRNA reduction with growth inhibition as the minimum transcript level required for 50% growth (MTL50). Mupirocin and globomycin, the protein inhibitors of IleS and LspA, respectively, were used in sensitization assays of strains containing both asRNA-expressing and open reading frame-expressing plasmids to examine deregulation of the overlapping ileS-lspA genes. We found upstream and downstream polar silencing effects when either ileS or lspA was silenced, indicating coupled expression. Weighted MTL50 values (means and standard deviations) of ribF, ileS, and lspA were 0.65 ± 0.18, 0.64 ± 0.06, and 0.76 ± 0.10, respectively. However, they were not significantly different (P = 0.71 by weighted one-way analysis of variance). The gene requirement for ispH could not be determined due to insufficient growth reduction. Mupirocin and globomycin sensitization experiments indicated that ileS-lspA expression could not be decoupled. The results highlight the inherent challenges associated with genetic analyses of operons; however, coupling of essential genes may provide opportunities to improve RNA-silencing antimicrobials.

Indexed as

Genes, EssentialGene SilencingOperonEscherichia coliGene ExpressionGene Knockdown TechniquesGenetic VectorsPlasmidsRNA, AntisenseRNA, Antisense

Identifiers

PMID26070674
PMCPMC4510190
OpenAlexW1788293483

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.