Evidence map›Paper›PMID 25882208›Full record

ArticleNature communications2015

Dietary sugar promotes systemic TOR activation in Drosophila through AKH-dependent selective secretion of Dilp3.

Jung Kim, Thomas P Neufeld

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2015. 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
7.5field-weighted citation impact, top 2% 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

87 citing papers in PubMed, 185 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Pss knockdown in the midgut causes growth retardation in Drosophila similar to that in human LMHD.Developmental dynamics : an official publication of the American Association of Anatomists · 2026
    Article
  5. Article
  6. Article
  7. Article
  8. Lipid Metabolism in Relation to Carbohydrate Metabolism.Advances in experimental medicine and biology · 2026
    Review
  9. Article
  10. The insulin-like peptides Dilp2 and Dilp6 exhibit divergent responses to dietary sugar and protein inProceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  11. Article
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  13. Article
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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

2 authors at 1 institution in 1 country.

Jung KimDepartment of Genetics, Cell Biology and Development, University of Minnesota, 6-160 Jackson Hall, 321 Church St SE, Minneapolis, Minnesota 55455, USA.
Thomas P NeufeldDepartment of Genetics, Cell Biology and Development, University of Minnesota, 6-160 Jackson Hall, 321 Church St SE, Minneapolis, Minnesota 55455, USA.
University of Minnesota · US

Funding

Regulation of TOR Signaling and Autophagy in DrosophilaR01GM062509 · NIGMS · UNIVERSITY OF MINNESOTA TWIN CITIES · PI NEUFELD, THOMAS P. · 2001 to 2013
$3.8M
NIGMS NIH HHS R01 GM062509NIGMS NIH HHS R01 GM62509
6 · The paper itself

Abstract

Secreted ligands of the insulin family promote cell growth and maintain sugar homeostasis. Insulin release is tightly regulated in response to dietary conditions, but how insulin-producing cells (IPCs) coordinate their responses to distinct nutrient signals is unclear. Here we show that regulation of insulin secretion in Drosophila larvae has been segregated into distinct branches-whereas amino acids promote the secretion of Drosophila insulin-like peptide 2 (Dilp2), circulating sugars promote the selective release of Dilp3. Dilp3 is uniquely required for the sugar-mediated activation of TOR signalling and suppression of autophagy in the larval fat body. Sugar levels are not sensed directly by the IPCs, but rather by the adipokinetic hormone (AKH)-producing cells of the corpora cardiaca, and we demonstrate that AKH signalling is required in the IPCs for sugar-dependent Dilp3 release. Thus, IPCs integrate multiple cues to regulate the secretion of distinct insulin subtypes under varying nutrient conditions.

Indexed as

AnimalsAutophagyCorpora AllataDietary SucroseDrosophila melanogasterDrosophila ProteinsInsect HormonesInsulin-Secreting CellsIntercellular Signaling Peptides and ProteinsLarvaOligopeptidesPyrrolidonecarboxylic AcidSignal TransductionTOR Serine-Threonine KinasesDAKH peptideDietary SucroseDrosophila ProteinsILP3 protein, DrosophilaInsect HormonesIntercellular Signaling Peptides and ProteinsOligopeptidesPyrrolidonecarboxylic Acidtarget of rapamycin protein, DrosophilaTOR Serine-Threonine Kinases

Identifiers

PMID25882208
PMCPMC4402654
OpenAlexW2149200224

What OpenQuestion holds

Textmetadata
LicenceTDM
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.