Evidence map›Paper›PMID 31286408›Full record

ArticleJournal of molecular neuroscience : MN2019

Selection of Reference Genes for Normalization of Gene Expression Data in Blood of Machado-Joseph Disease/Spinocerebellar Ataxia Type 3 (MJD/SCA3) Subjects.

Ana F Ferreira, Mafalda Raposo, João Vasconcelos, Maria do Carmo Costa, Manuela Lima

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In one paragraph

Article in Journal of molecular neuroscience : MN, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.8field-weighted citation impact, top 29% 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

3 citing papers in PubMed, 12 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

5 authors at 3 institutions in 3 countries.

Ana F FerreiraFaculdade de Ciências e Tecnologia, Universidade dos Açores, Ponta Delgada, Portugal. ana.fb.ferreira@uac.pt.ORCID http://orcid.org/0000-0001-9839-3364
Mafalda RaposoFaculdade de Ciências e Tecnologia, Universidade dos Açores, Ponta Delgada, Portugal.
João VasconcelosServiço de Neurologia, Hospital Divino Espírito Santo, Ponta Delgada, Portugal.
Maria do Carmo CostaDepartment of Neurology, Michigan Medicine, University of Michigan, Ann Arbor, MI, USA.
Manuela LimaFaculdade de Ciências e Tecnologia, Universidade dos Açores, Ponta Delgada, Portugal.
Universidade dos Açores · PTHospital do Divino Espírito Santo · PTMichigan Medicine · US

Funding

EU Joint Programme - Neurodegenerative Disease Research JPCOFUND/0002/2015Fundação para a Ciência e a Tecnologia PTDC/DTP-PIC/0370/2012Fundação para a Ciência e a Tecnologia SFRH/BD/121101/2016
6 · The paper itself

Abstract

Alongside with the emergent clinical trials for Machado-Joseph disease/Spinocerebellar ataxia type 3 (MJD/SCA3) comes the need to identify molecular biomarkers of disease that can be tracked throughout the trial. MJD is an autosomal dominant neurodegenerative disorder caused by expansion of a CAG repeat in the coding region of the ATXN3 gene. Previous findings indicate the potential of transcriptional alterations in blood of MJD patients as biomarkers of disease. Accurate quantification of gene expression levels by quantitative real-time PCR (qPCR) depends on data normalization, usually performed using reference genes. Because the expression level of routinely used housekeeping genes may vary in multiple biological and experimental conditions, reference gene controls should be validated in each specific experimental design. Here, we aimed to evaluate the expression behavior of five housekeeping genes previously reported as stably expressed in peripheral blood of patients from several disorders-peptidylprolyl isomerase B (PPIB), TNF receptor associated protein 1 (TRAP1), beta-2-microglobulin (B2M), 2,4-dienoyl-CoA reductase 1 (DECR1), and folylpolyglutamate synthase (FPGS). Expression levels of these five genes were assessed by qPCR in blood from MJD subjects (preataxic and patients) and matched controls. While all housekeeping genes, here studied, were stably expressed in our sets of samples, TRAP1 showed to be the most stable gene by NormFinder and BestKeeper. We, therefore, conclude that any of these genes could be used as reference gene in future qPCR studies using blood samples from MJD subjects.

Indexed as

Gene ExpressionAdultbeta 2-MicroglobulinCase-Control StudiesCyclophilinsFemaleHSP90 Heat-Shock ProteinsHumansMachado-Joseph DiseaseMaleMiddle AgedOxidoreductases Acting on CH-CH Group DonorsPeptide SynthasesReal-Time Polymerase Chain ReactionReference StandardsYoung Adult2,4-dienoyl-CoA reductasebeta 2-Microglobulincyclophilin BCyclophilinsfolylpolyglutamate synthetaseHSP90 Heat-Shock ProteinsOxidoreductases Acting on CH-CH Group DonorsPeptide SynthasesTRAP1 protein, humanAtaxiaATXN3Housekeeping genePolyglutamineTranscriptional biomarkersTRAP1

Identifiers

PMID31286408
OpenAlexW2956148613

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.