Evidence map›Paper›PMID 31077566›Full record

ArticleFEBS open bio2019

Evaluation of critical design parameters for RT-qPCR-based analysis of multiple dUTPase isoform genes in mice.

Gergely A Rácz, Nikolett Nagy, Zoltán Gál, Tímea Pintér, László Hiripi, Beáta G Vértessy

Open access · goldAbstract readEvaluation Study
In one paragraph

Article in FEBS open bio, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.3field-weighted citation impact, top 44% 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

5 citing papers in PubMed, 7 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

6 authors at 6 institutions in 1 country.

Gergely A RáczInstitute of Enzymology, RCNS, Hungarian Academy of Sciences, Budapest, Hungary.
Nikolett NagyInstitute of Enzymology, RCNS, Hungarian Academy of Sciences, Budapest, Hungary.
Zoltán GálDepartment of Animal Biotechnology, Agricultural Biotechnology Institute, National Agricultural Research and Innovation Centre, Gödöllő, Hungary.
Tímea PintérDepartment of Animal Biotechnology, Agricultural Biotechnology Institute, National Agricultural Research and Innovation Centre, Gödöllő, Hungary.
László HiripiDepartment of Animal Biotechnology, Agricultural Biotechnology Institute, National Agricultural Research and Innovation Centre, Gödöllő, Hungary.
Beáta G VértessyInstitute of Enzymology, RCNS, Hungarian Academy of Sciences, Budapest, Hungary.
Agricultural Biotechnology Institute · HUBudapest University of Technology and Economics · HUHungarian Academy of Sciences · HUInstitute of Molecular Life Sciences · HUMagyar Agrár- és Élettudományi Egyetem · HUNational Agricultural Research and Innovation Centre · HU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The coupling of nucleotide biosynthesis and genome integrity plays an important role in ensuring faithful maintenance and transmission of genetic information. The enzyme dUTPase is a prime example of such coupling, as it generates dUMP for thymidylate biosynthesis and removes dUTP for synthesis of uracil-free DNA. Despite its significant role, the expression patterns of dUTPase isoforms in animals have not yet been described. Here, we developed a detailed optimization procedure for RT-qPCR-based isoform-specific analysis of dUTPase expression levels in various organs of adult mice. Primer design, optimal annealing temperature, and primer concentrations were specified for both nuclear and mitochondrial dUTPase isoforms, as well as two commonly used reference genes, GAPDH and PPIA. The linear range of the RNA concentration for the reverse transcription reaction was determined. The PCR efficiencies were calculated using serial dilutions of cDNA. Our data indicate that organs involved in lymphocyte production, as well as reproductive organs, are characterized by high levels of expression of the nuclear dUTPase isoform. On the other hand, we observed that expression of the mitochondrial dUTPase isoform is considerably increased in heart, kidney, and ovary. Despite the differences in expression levels among the various organs, we also found that the mitochondrial dUTPase isoform shows a much more uniform expression pattern as compared to the reference genes GAPDH and PPIA.

Indexed as

TranscriptomeAnimalsCell NucleusDeoxyuracil NucleotidesDNA, ComplementaryDNA PrimersFemaleIsoenzymesKidneyMaleMiceMitochondriaMyocardiumOsmolar ConcentrationOvaryPyrophosphatasesDeoxyuracil Nucleotidesdeoxyuridine triphosphateDNA, ComplementaryDNA PrimersdUTP pyrophosphataseIsoenzymesPyrophosphatasesdUTPaseisoform-specific expression levelsmitochondrial dUTPase isoformmouse organsnuclear dUTPase isoformRT-qPCR optimization

Identifiers

PMID31077566
PMCPMC6551494
OpenAlexW2944084410

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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.