Evidence map›Paper›PMID 24914188›Full record

ArticleJournal of bacteriology2014

Selection of dinB alleles suppressing survival loss upon dinB overexpression in Escherichia coli.

Ryan W Benson, Tiziana M Cafarelli, Thomas J Rands, Ida Lin, Veronica G Godoy

Abstract read
In one paragraph

Article in Journal of bacteriology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. RNA Primer Extension Hinders DNA Synthesis byFrontiers in microbiology · 2017
    Article
  6. Article
  7. 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

5 authors.

Ryan W BensonDepartment of Biology, Northeastern University, Boston, Massachusetts, USA.
Tiziana M CafarelliDepartment of Biology, Northeastern University, Boston, Massachusetts, USA.
Thomas J RandsDepartment of Biology, Northeastern University, Boston, Massachusetts, USA.
Ida LinDepartment of Biology, Northeastern University, Boston, Massachusetts, USA.
Veronica G GodoyDepartment of Biology, Northeastern University, Boston, Massachusetts, USA v.godoycarter@neu.edu.

Funding

FORSYTH POSTDOCTORAL TRAINING IN ORAL HEALTH RESEARCHT32DE007327 · NIDCR · FORSYTH INSTITUTE · PI VAN DYKE, THOMAS ELLIOTT · 2001 to 2015
$3.5M
Mechanisms to control the activity of low fidelity DNA polymerases.R01GM088230 · NIGMS · NORTHEASTERN UNIVERSITY · PI GODOY-CARTER, S. VERONICA · 2010 to 2014
$1.7M
NIDCR NIH HHS T32 DE007327NIGMS NIH HHS R01 GM088230NIGMS NIH HHS R01GM088230
6 · The paper itself

Abstract

Escherichia coli strains overproducing DinB undergo survival loss; however, the mechanisms regulating this phenotype are poorly understood. Here we report a genetic selection revealing DinB residues essential to effect this loss-of-survival phenotype. The selection uses strains carrying both an antimutator allele of DNA polymerase III (Pol III) α-subunit (dnaE915) and either chromosomal or plasmid-borne dinB alleles. We hypothesized that dnaE915 cells would respond to DinB overproduction differently from dnaE(+) cells because the dnaE915 allele is known to have an altered genetic interaction with dinB(+) compared to its interaction with dnaE(+). Notably, we observe a loss-of-survival phenotype in dnaE915 strains with either a chromosomal catalytically inactive dinB(D103N) allele or a low-copy-number plasmid-borne dinB(+) upon DNA damage treatment. Furthermore, we find that the loss-of-survival phenotype occurs independently of DNA damage treatment in a dnaE915 strain expressing the catalytically inactive dinB(D103N) allele from a low-copy-number plasmid. The selective pressure imposed resulted in suppressor mutations that eliminated growth defects. The dinB intragenic mutations examined were either base pair substitutions or those that we inferred to be loss of function (i.e., deletions and insertions). Further analyses of selected novel dinB alleles, generated by single-base-pair substitutions in the dnaE915 strain, indicated that these no longer effect loss of survival upon overproduction in dnaE(+) strains. These mutations are mapped to specific areas of DinB; this permits us to gain insights into the mechanisms underlying the DinB-mediated overproduction loss-of-survival phenotype.

Indexed as

Gene ExpressionMicrobial ViabilitySelection, GeneticAllelesDNA Mutational AnalysisEscherichia coliEscherichia coli ProteinsModels, MolecularMutagenesis, InsertionalMutant ProteinsPlasmidsPoint MutationProtein ConformationSequence DeletionSuppression, GeneticDinB protein, E coliEscherichia coli ProteinsMutant Proteins

Identifiers

PMID24914188
PMCPMC4135642

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.