Evidence map›Paper›PMID 29240933›Full record

ArticleNucleic acids research2018

Recruitment of UvrBC complexes to UV-induced damage in the absence of UvrA increases cell survival.

Luke Springall, Craig D Hughes, Michelle Simons, Stavros Azinas, Bennett Van Houten, Neil M Kad

Abstract read
In one paragraph

Article in Nucleic acids research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. Comparative genome analysis and secondary biosynthetic potential of the Streptomyces microflavus strains isolated from high altitude.Brazilian journal of microbiology : [publication of the Brazilian Society for Microbiology] · 2026
    Article
  2. Article
  3. Article
  4. Article
  5. Resolving the subtle details of human DNA alkyltransferase lesion search and repair mechanism by single-molecule studies.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  6. Article
  7. Review
  8. Review
  9. Review
  10. A Peek Inside the Machines of Bacterial Nucleotide Excision Repair.International journal of molecular sciences · 2021
    Review
  11. Review
  12. Review
  13. Understanding the coupling between DNA damage detection and UvrA's ATPase using bulk and single molecule kinetics.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2019
    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.

Luke SpringallSchool of Biological Sciences, University of Kent, Canterbury CT2 7NH, UK.
Craig D HughesDepartment of Veterinary Medicine, University of Cambridge, Cambridge CB3 0ES, UK.
Michelle SimonsSchool of Biological Sciences, University of Essex, Colchester CO4 3SQ, UK.
Stavros AzinasSchool of Biological Sciences, University of Essex, Colchester CO4 3SQ, UK.
Bennett Van HoutenUPMC Hillman Cancer Center, Pittsburgh, PA 15213, USA.
Neil M KadSchool of Biological Sciences, University of Kent, Canterbury CT2 7NH, UK.

Funding

DNA damage recognition by nucleotide excision repair proteinsR01ES019566 · NIEHS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI VAN HOUTEN, BENNETT · 2011 to 2020
$3.9M
MEMBRANE CHANGES CAUSED BY TUMOR VIRUS TRANSFORMATIONR01CA019144 · NCI · WISTAR INSTITUTE · PI BUCK, CLAYTON A · 1985 to 1988
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MEMBRANE CHANGES CAUSED BY TUMOR VIRUS TRANSFORMATIONR37CA019144 · NCI · WISTAR INSTITUTE · PI BUCK, CLAYTON A · 1989 to 1997
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Biotechnology and Biological Sciences Research Council BB/I003460/1Biotechnology and Biological Sciences Research Council BB/M019144/1Biotechnology and Biological Sciences Research Council BB/P00847X/1NIEHS NIH HHS R01 ES019566
6 · The paper itself

Abstract

Nucleotide excision repair (NER) is the primary mechanism for removal of ultraviolet light (UV)-induced DNA photoproducts and is mechanistically conserved across all kingdoms of life. Bacterial NER involves damage recognition by UvrA2 and UvrB, followed by UvrC-mediated incision either side of the lesion. Here, using a combination of in vitro and in vivo single-molecule studies we show that a UvrBC complex is capable of lesion identification in the absence of UvrA. Single-molecule analysis of eGFP-labelled UvrB and UvrC in living cells showed that UV damage caused these proteins to switch from cytoplasmic diffusion to stable complexes on DNA. Surprisingly, ectopic expression of UvrC in a uvrA deleted strain increased UV survival. These data provide evidence for a previously unrealized mechanism of survival that can occur through direct lesion recognition by a UvrBC complex.

Indexed as

DNA RepairAdenosine TriphosphatasesBacillusDNA, BacterialDNA-Binding ProteinsDNA DamageDNA HelicasesEndodeoxyribonucleasesEscherichia coliEscherichia coli ProteinsGene DeletionGene Expression Regulation, BacterialGenes, ReporterGreen Fluorescent ProteinsMicrobial ViabilityProtein BindingAdenosine TriphosphatasesDNA, BacterialDNA-Binding ProteinsDNA HelicasesEndodeoxyribonucleasesenhanced green fluorescent proteinEscherichia coli ProteinsGreen Fluorescent ProteinsUvrA protein, E coliUvrB protein, E coliUvrC protein, E coli

Identifiers

PMID29240933
PMCPMC5814901

What OpenQuestion holds

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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.