Evidence map›Paper›PMID 23775797›Full record

ArticleNucleic acids research2013

Comet-FISH with strand-specific probes reveals transcription-coupled repair of 8-oxoGuanine in human cells.

Jia Guo, Philip C Hanawalt, Graciela Spivak

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 65 papers.

0numbers the graph read from it
0cells of the map it votes in
65citing papers in PubMed
5.4field-weighted citation impact, top 3% 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

65 citing papers in PubMed, 99 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. 8-Oxoguanine: A Lesion, an Epigenetic Mark, or a Molecular Signal?International journal of molecular sciences · 2025
    Review
  5. Article
  6. Review
  7. Review
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Review
  16. Nucleotide excision repair: a versatile and smart toolkit.Acta biochimica et biophysica Sinica · 2022
    Review
  17. Article
  18. Review
  19. Analysis of DNA Double-Stranded Breaks Using the Comet Assay in Planarians.Methods in molecular biology (Clifton, N.J.) · 2022
    Article
  20. DNA glycosylase NEIL2 functions in multiple cellular processes.Progress in biophysics and molecular biology · 2021
    Review

5 more citing papers are in PubMed but not listed here.

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

3 authors at 1 institution in 1 country.

Jia GuoDepartment of Biology, Stanford University, 371 Serra Mall, Stanford, CA 94305-5020, USA.
Philip C Hanawalt
Graciela Spivak
Stanford University · US

Funding

Oxidative DNA damage processing; role in human pathology and agingR01ES018834 · NIEHS · STANFORD UNIVERSITY · PI HANAWALT, PHILIP COURTLAND · 2010 to 2014
$1.7M
NIEHS NIH HHS ES018834NIEHS NIH HHS R01 ES018834
6 · The paper itself

Abstract

Oxidized bases in DNA have been implicated in cancer, aging and neurodegenerative disease. We have developed an approach combining single-cell gel electrophoresis (comet) with fluorescence in situ hybridization (FISH) that enables the comparative quantification of low, physiologically relevant levels of DNA lesions in the respective strands of defined nucleotide sequences and in the genome overall. We have synthesized single-stranded probes targeting the termini of DNA segments of interest using a polymerase chain reaction-based method. These probes facilitate detection of damage at the single-molecule level, as the lesions are converted to DNA strand breaks by lesion-specific endonucleases or glycosylases. To validate our method, we have documented transcription-coupled repair of cyclobutane pyrimidine dimers in the ataxia telangiectasia-mutated (ATM) gene in human fibroblasts irradiated with 254 nm ultraviolet at 0.1 J/m2, a dose ∼100-fold lower than those typically used. The high specificity and sensitivity of our approach revealed that 7,8-dihydro-8-oxoguanine (8-oxoG) at an incidence of approximately three lesions per megabase is preferentially repaired in the transcribed strand of the ATM gene. We have also demonstrated that the hOGG1, XPA, CSB and UVSSA proteins, as well as actively elongating RNA polymerase II, are required for this process, suggesting cross-talk between DNA repair pathways.

Indexed as

DNA RepairTranscription, GeneticAtaxia Telangiectasia Mutated ProteinsCarrier ProteinsCell Cycle ProteinsCell LineComet AssayDNA-Binding ProteinsDNA HelicasesDNA ProbesDNA Repair EnzymesGuanineHumansIn Situ Hybridization, FluorescencePoly-ADP-Ribose Binding ProteinsProtein Serine-Threonine Kinases8-hydroxyguanineAtaxia Telangiectasia Mutated ProteinsATM protein, humanCarrier ProteinsCell Cycle ProteinsDNA-Binding ProteinsDNA HelicasesDNA ProbesDNA Repair EnzymesERCC6 protein, humanGuaninePoly-ADP-Ribose Binding ProteinsProtein Serine-Threonine KinasesPyrimidine DimersRNA Polymerase IITumor Suppressor ProteinsUVSSA protein, human

Identifiers

PMID23775797
PMCPMC3763531
OpenAlexW2054419107

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.