Evidence map›Paper›PMID 22068330›Full record

ArticleMolecular systems biology2011

Modularity and hormone sensitivity of the Drosophila melanogaster insulin receptor/target of rapamycin interaction proteome.

Timo Glatter, Ralf B Schittenhelm, Oliver Rinner, Katarzyna Roguska, Alexander Wepf, Martin A Jünger, Katja Köhler, Irena Jevtov, Hyungwon Choi, Alexander Schmidt and 5 more

Open access · goldAbstract read
In one paragraph

Article in Molecular systems biology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
3.3field-weighted citation impact, top 7% 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

41 citing papers in PubMed, 62 citations in OpenAlex.

  1. Article
  2. Review
  3. International journal of molecular sciences · 2022
    Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. On the Fly: Recent Progress on Autophagy and Aging in Drosophila.Frontiers in cell and developmental biology · 2019
    Review
  11. Article
  12. Article
  13. Review
  14. BioMed research international · 2018
    Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Regulation of mTORC1 by PI3K signaling.Trends in cell biology · 2015
    Review
  20. 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

15 authors at 4 institutions in 2 countries.

Timo GlatterDepartment of Biology, Institute of Molecular Systems Biology, ETH Zurich, Zurich, Switzerland.
Ralf B Schittenhelm
Oliver Rinner
Katarzyna Roguska
Alexander Wepf
Martin A Jünger
Katja Köhler
Irena Jevtov
Hyungwon Choi
Alexander Schmidt
Alexey I Nesvizhskii
Hugo Stocker
Ernst Hafen
Ruedi Aebersold
Matthias Gstaiger
ETH Zurich · CHMichigan Medicine · USUniversity of Basel · CHUniversity of Zurich · CH

Funding

COMPUTATIONAL TOOLS FOR MASS SPECTROMETRY-BASED INTERACTOME DATAR01GM094231 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Alexey I Nesvizhskii · 2010 to 2026
$5.4M
NIGMS NIH HHS R01 GM094231
6 · The paper itself

Abstract

Genetic analysis in Drosophila melanogaster has been widely used to identify a system of genes that control cell growth in response to insulin and nutrients. Many of these genes encode components of the insulin receptor/target of rapamycin (InR/TOR) pathway. However, the biochemical context of this regulatory system is still poorly characterized in Drosophila. Here, we present the first quantitative study that systematically characterizes the modularity and hormone sensitivity of the interaction proteome underlying growth control by the dInR/TOR pathway. Applying quantitative affinity purification and mass spectrometry, we identified 97 high confidence protein interactions among 58 network components. In all, 22% of the detected interactions were regulated by insulin affecting membrane proximal as well as intracellular signaling complexes. Systematic functional analysis linked a subset of network components to the control of dTORC1 and dTORC2 activity. Furthermore, our data suggest the presence of three distinct dTOR kinase complexes, including the evolutionary conserved dTTT complex (Drosophila TOR, TELO2, TTI1). Subsequent genetic studies in flies suggest a role for dTTT in controlling cell growth via a dTORC1- and dTORC2-dependent mechanism.

Indexed as

AnimalsCell LineDrosophila melanogasterDrosophila ProteinsMass SpectrometryProtein Interaction MapsProtein KinasesProteomeReceptor, InsulinSignal TransductionTOR Serine-Threonine KinasesTranscription FactorsDrosophila ProteinsProtein KinasesProteomeReceptor, Insulintarget of rapamycin protein, DrosophilaTOR Serine-Threonine KinasesTranscription Factors

Identifiers

PMID22068330
PMCPMC3261712
OpenAlexW2161010425

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.