Evidence map›Paper›PMID 25821834›Full record

ArticleJournal of diabetes research2015

Use of Drosophila as an evaluation method reveals imp as a candidate gene for type 2 diabetes in rat locus Niddm22.

Kurenai Kawasaki, Sawaka Yamada, Koki Ogata, Yumiko Saito, Aiko Takahama, Takahisa Yamada, Kozo Matsumoto, Hiroyuki Kose

Open access · goldAbstract read
In one paragraph

Article in Journal of diabetes research, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.1field-weighted citation impact, top 52% 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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. Examination ofJournal of genetics · 2022
    Article
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

8 authors at 3 institutions in 1 country.

Kurenai KawasakiDivision of Natural Sciences, Department of Life Science, International Christian University, Mitaka, Tokyo 181-8585, Japan.
Sawaka YamadaDivision of Natural Sciences, Department of Life Science, International Christian University, Mitaka, Tokyo 181-8585, Japan.
Koki OgataDivision of Natural Sciences, Department of Life Science, International Christian University, Mitaka, Tokyo 181-8585, Japan.
Yumiko SaitoDivision of Natural Sciences, Department of Life Science, International Christian University, Mitaka, Tokyo 181-8585, Japan.
Aiko TakahamaDivision of Natural Sciences, Department of Life Science, International Christian University, Mitaka, Tokyo 181-8585, Japan.
Takahisa YamadaLaboratory of Animal Genetics, Graduate School of Science and Technology, Niigata University, Niigata 950-2181, Japan.ORCID 0000-0003-2800-4989
Kozo MatsumotoDepartment of Animal Medical Sciences, Faculty of Life Sciences, Kyoto Sangyo University, Kyoto 603-8555, Japan.
Hiroyuki KoseDivision of Natural Sciences, Department of Life Science, International Christian University, Mitaka, Tokyo 181-8585, Japan.ORCID 0000-0001-9462-0873
International Christian University · JPKyoto Sangyo University · JPNiigata University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Type 2 diabetes (T2D) is one of the most common human diseases. QTL analysis of the diabetic Otsuka Long-Evans Tokushima Fatty (OLETF) rats has identified numerous hyperglycemic loci. However, molecular characterization and/or gene identification largely remains to be elucidated due mostly to the weak genetic variances contributed by each locus. Here we utilized Drosophila melanogaster as a secondary model organism for functional evaluation of the candidate gene. We demonstrate that the tissue specific knockdown of a homologue of igf2bp2 RNA binding protein leads to increased sugar levels similar to that found in the OLETF rat. In the mutant, the expression of two of the insulin-like peptides encoded in the fly genome, dilp2 and dilp3, were found to be downregulated. Consistent with previous reports of dilp mutants, the imp mutant flies exhibited an extension of life span; in contrast, starvation tolerance was reduced. These results further reinforce the possibility that imp is involved in sugar metabolism by modulating insulin expression.

Indexed as

AnimalsBlood GlucoseBody WeightDiabetes Mellitus, Type 2Disease Models, AnimalDrosophila melanogasterDrosophila ProteinsFemaleGene Expression ProfilingGreen Fluorescent ProteinsHyperglycemiaInsulinInsulin-Like Growth Factor Binding Protein 2MalePolymorphism, GeneticRatsBlood GlucoseDrosophila ProteinsGreen Fluorescent ProteinsInsulinInsulin-Like Growth Factor Binding Protein 2

Identifiers

PMID25821834
PMCPMC4363715
OpenAlexW2052634311

What OpenQuestion holds

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LicenceCC BY
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.