Evidence map›Paper›PMID 28116036›Full record

ArticleOxidative medicine and cellular longevity2016

Conservation of the Nrf2-Mediated Gene Regulation of Proteasome Subunits and Glucose Metabolism in Zebrafish.

Vu Thanh Nguyen, Yuji Fuse, Junya Tamaoki, Shin-Ichi Akiyama, Masafumi Muratani, Yutaka Tamaru, Makoto Kobayashi

Open access · hybridAbstract read
In one paragraph

Article in Oxidative medicine and cellular longevity, 2016. 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
1.0field-weighted citation impact, top 21% 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

13 citing papers in PubMed, 27 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

7 authors at 2 institutions in 1 country.

Vu Thanh NguyenDepartment of Molecular and Developmental Biology, Faculty of Medicine, University of Tsukuba, Tsukuba 305-8575, Japan; Doctoral Program in Biomedical Sciences, Graduate School of Comprehensive Human Sciences, University of Tsukuba, Tsukuba 305-8575, Japan.ORCID 0000-0002-3458-8813
Yuji FuseDepartment of Molecular and Developmental Biology, Faculty of Medicine, University of Tsukuba, Tsukuba 305-8575, Japan; Doctoral Program in Biomedical Sciences, Graduate School of Comprehensive Human Sciences, University of Tsukuba, Tsukuba 305-8575, Japan.
Junya TamaokiDepartment of Molecular and Developmental Biology, Faculty of Medicine, University of Tsukuba, Tsukuba 305-8575, Japan; College of Biological Sciences, University of Tsukuba, Tsukuba 305-8575, Japan.
Shin-Ichi AkiyamaDivision of Nephrology, Department of Internal Medicine, Nagoya University Graduate School of Medicine, Nagoya 466-8550, Japan; Department of Life Sciences, Graduate School of Bioresources, Mie University, Tsu 514-8507, Japan.
Masafumi MurataniDepartment of Genome Biology, Faculty of Medicine, University of Tsukuba, Tsukuba 305-8575, Japan.
Yutaka TamaruDepartment of Life Sciences, Graduate School of Bioresources, Mie University, Tsu 514-8507, Japan.ORCID 0000-0003-0803-4830
Makoto KobayashiDepartment of Molecular and Developmental Biology, Faculty of Medicine, University of Tsukuba, Tsukuba 305-8575, Japan.ORCID 0000-0001-6660-450X
University of Tsukuba · JPMie University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The Keap1-Nrf2 system is an evolutionarily conserved defense mechanism against oxidative and xenobiotic stress. Besides the exogenous stress response, Nrf2 has been found to regulate numerous cellular functions, including protein turnover and glucose metabolism; however, the evolutionary origins of these functions remain unknown. In the present study, we searched for novel target genes associated with the zebrafish Nrf2 to answer this question. A microarray analysis of zebrafish embryos that overexpressed Nrf2 revealed that 115 candidate genes were targets of Nrf2, including genes encoding proteasome subunits and enzymes involved in glucose metabolism. A real-time quantitative PCR suggested that the expression of 3 proteasome subunits (

Indexed as

AnimalsGene Expression RegulationGlucoseIn Situ HybridizationLarvaLiverNF-E2-Related Factor 2Oligonucleotide Array Sequence AnalysisProteasome Endopeptidase ComplexProtein SubunitsReal-Time Polymerase Chain ReactionUp-RegulationZebrafishZebrafish ProteinsGlucosenfe2l2a protein, zebrafishNF-E2-Related Factor 2Proteasome Endopeptidase ComplexProtein SubunitsZebrafish Proteins

Identifiers

PMID28116036
PMCPMC5223048
OpenAlexW2564998349

What OpenQuestion holds

Textmetadata
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.