Evidence map›Paper›PMID 30673695›Full record

ArticlePloS one2019

A variant of the Escherichia coli anaerobic transcription factor FNR exhibiting diminished promoter activation function enhances ionizing radiation resistance.

Steven T Bruckbauer, Joseph D Trimarco, Camille Henry, Elizabeth A Wood, John R Battista, Michael M Cox

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2019. 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
0.3field-weighted citation impact, top 45% 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, 4 citations in OpenAlex.

  1. Article
  2. Review
  3. Physiology of Highly RadioresistantFrontiers in microbiology · 2020
    Article
  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

6 authors at 2 institutions in 1 country.

Steven T BruckbauerDepartment of Biochemistry, University of Wisconsin - Madison, Madison, Wisconsin, United States of America.ORCID 0000-0002-1684-8466
Joseph D TrimarcoDepartment of Biochemistry, University of Wisconsin - Madison, Madison, Wisconsin, United States of America.
Camille HenryDepartment of Biochemistry, University of Wisconsin - Madison, Madison, Wisconsin, United States of America.
Elizabeth A WoodDepartment of Biochemistry, University of Wisconsin - Madison, Madison, Wisconsin, United States of America.
John R BattistaDepartment of Biological Sciences, Louisiana State University and A & M College, Baton Rouge, Louisiana, United States of America.
Michael M CoxDepartment of Biochemistry, University of Wisconsin - Madison, Madison, Wisconsin, United States of America.
University of Wisconsin–Madison · USLouisiana State University · US

Funding

Molecular basis of ionizing radiation resistanceR01GM112757 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI COX, MICHAEL M. · 2017 to 2020
$1.2M
NIGMS NIH HHS R01 GM112757
6 · The paper itself

Abstract

We have previously generated four replicate populations of ionizing radiation (IR)-resistant Escherichia coli though directed evolution. Sequencing of isolates from these populations revealed that mutations affecting DNA repair (through DNA double-strand break repair and replication restart), ROS amelioration, and cell wall metabolism were prominent. Three mutations involved in DNA repair explained the IR resistance phenotype in one population, and similar DNA repair mutations were prominent in two others. The remaining population, IR-3-20, had no mutations in the key DNA repair proteins, suggesting that it had taken a different evolutionary path to IR resistance. Here, we present evidence that a variant of the anaerobic metabolism transcription factor FNR, unique to and isolated from population IR-3-20, plays a role in IR resistance. The F186I allele of FNR exhibits a diminished ability to activate transcription from FNR-activatable promoters, and furthermore reduces levels of intracellular ROS. The FNR F186I variant is apparently capable of enhancing resistance to IR under chronic irradiation conditions, but does not increase cell survival when exposed to acute irradiation. Our results underline the importance of dose rate on cell survival of IR exposure.

Indexed as

Gamma RaysMutation, MissensePromoter Regions, GeneticRadiation ToleranceAmino Acid SubstitutionEscherichia coliEscherichia coli ProteinsGene Expression Regulation, BacterialIron-Sulfur ProteinsEscherichia coli ProteinsFNR protein, E coliIron-Sulfur Proteins

Identifiers

PMID30673695
PMCPMC6343905
OpenAlexW2911871570

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.