Evidence map›Paper›PMID 20123023›Full record

ReviewMethods (San Diego, Calif.)2010

The QPCR assay for analysis of mitochondrial DNA damage, repair, and relative copy number.

Senyene E Hunter, Dawoon Jung, Richard T Di Giulio, Joel N Meyer

Abstract readReview
In one paragraph

Review in Methods (San Diego, Calif.), 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 87 papers.

0numbers the graph read from it
0cells of the map it votes in
87citing 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

87 citing papers in PubMed.

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  15. Frontiers in neuroscience · 2023
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27 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

4 authors.

Senyene E HunterNicholas School of the Environment, Duke University, Durham, NC 27708-0328, USA.
Dawoon Jung
Richard T Di Giulio
Joel N Meyer

Funding

Zebrafish as a Detector of Organophosphate ExposureP42ES010356 · NIEHS · DUKE UNIVERSITY · PI EDWARD D LEVIN · 2000 to 2026
$56.2M
Molecular and Physiological Responses to Persistent Mitochondrial DNA DamageR21NS065468 · NINDS · DUKE UNIVERSITY · PI MEYER, JOEL NEWMAN · 2009 to 2010
$421k
NIEHS NIH HHS P42 ES010356NIEHS NIH HHS P42 ES10356NINDS NIH HHS R21 NS065468
6 · The paper itself

Abstract

The quantitative polymerase chain reaction (QPCR) assay allows measurement of DNA damage in the mitochondrial and nuclear genomes without isolation of mitochondria. It also permits measurement of relative mitochondrial genome copy number. Finally, it can be used for measurement of DNA repair in vivo when employed appropriately. In this manuscript we briefly review the methodology of the QPCR assay, discuss its strengths and limitations, address considerations for measurement of mitochondrial DNA repair, and describe methodological changes implemented in recent years. We present QPCR assay primers and reaction conditions for five species not previously described in a methods article: Caenorhabditis elegans, Fundulus heteroclitus, Danio rerio, Drosophila melanogaster, and adenovirus. Finally, we illustrate the use of the assay by measuring repair of ultraviolet C radiation-induced DNA damage in the nuclear but not mitochondrial genomes of a zebrafish cell culture.

Indexed as

DNA DamageDNA RepairAnimalsBase SequenceDNA, MitochondrialDNA PrimersGene DosageGenome, MitochondrialHumansMitochondriaPolymerase Chain ReactionDNA, MitochondrialDNA Primers

Identifiers

PMID20123023
PMCPMC2912960

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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.