Evidence map›Paper›PMID 25878065›Full record

ArticleG3 (Bethesda, Md.)2015

Mutations that Separate the Functions of the Proofreading Subunit of the Escherichia coli Replicase.

Zakiya Whatley, Kenneth N Kreuzer

Open access · goldAbstract read
In one paragraph

Article in G3 (Bethesda, Md.), 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
0.3field-weighted citation impact, top 38% 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, 10 citations in OpenAlex.

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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

2 authors at 2 institutions in 1 country.

Zakiya WhatleyUniversity Program in Genetics and Genomics, Duke University, Durham, North Carolina 27705.
Kenneth N KreuzerUniversity Program in Genetics and Genomics, Duke University, Durham, North Carolina 27705 Department of Biochemistry, Duke University Medical Center, Durham, North Carolina 27710 kenneth.kreuzer@duke.edu.
Duke Medical Center · USDuke University · US

Funding

ORGANIZATION AND FUNCTIONS OF CELLULAR STRUCTUREST32GM007184 · NIGMS · DUKE UNIVERSITY · PI JINKS-ROBERTSON, SUE · 1985 to 2019
$18.2M
Processing and consequences of DNA-protein crosslinks in E. coliR01GM072089 · NIGMS · DUKE UNIVERSITY · PI KREUZER, KENNETH N · 2004 to 2012
$2.5M
NIGMS NIH HHS 5T32-GM007184NIGMS NIH HHS R01 GM072089NIGMS NIH HHS R01-GM72089NIGMS NIH HHS T32 GM007184
6 · The paper itself

Abstract

The dnaQ gene of Escherichia coli encodes the ε subunit of DNA polymerase III, which provides the 3' → 5' exonuclease proofreading activity of the replicative polymerase. Prior studies have shown that loss of ε leads to high mutation frequency, partially constitutive SOS, and poor growth. In addition, a previous study from our laboratory identified dnaQ knockout mutants in a screen for mutants specifically defective in the SOS response after quinolone (nalidixic acid) treatment. To explain these results, we propose a model whereby, in addition to proofreading, ε plays a distinct role in replisome disassembly and/or processing of stalled replication forks. To explore this model, we generated a pentapeptide insertion mutant library of the dnaQ gene, along with site-directed mutants, and screened for separation of function mutants. We report the identification of separation of function mutants from this screen, showing that proofreading function can be uncoupled from SOS phenotypes (partially constitutive SOS and the nalidixic acid SOS defect). Surprisingly, the two SOS phenotypes also appear to be separable from each other. These findings support the hypothesis that ε has additional roles aside from proofreading. Identification of these mutants, especially those with normal proofreading but SOS phenotype(s), also facilitates the study of the role of ε in SOS processes without the confounding results of high mutator activity associated with dnaQ knockout mutants.

Indexed as

Amino Acid MotifsAmino Acid SequenceDNA Polymerase IIIEscherichia coliEscherichia coli ProteinsMolecular Sequence DataMutagenesis, InsertionalMutagenesis, Site-DirectedMutationMutation RateNalidixic AcidPhenotypeProtein Structure, TertiaryProtein SubunitsSOS Response, GeneticsDNA Polymerase IIIdnaQ protein, E coliEscherichia coli ProteinsNalidixic AcidProtein SubunitsDNA polymeraseepsilon subunitlinker-scanning mutagenesismutation rateSOS response

Identifiers

PMID25878065
PMCPMC4478557
OpenAlexW2156582467

What OpenQuestion holds

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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.