Evidence map›Paper›PMID 25920570›Full record

ArticleDevelopmental cell2015

REPTOR and REPTOR-BP Regulate Organismal Metabolism and Transcription Downstream of TORC1.

Marcel Tiebe, Marilena Lutz, Adriana De La Garza, Tina Buechling, Michael Boutros, Aurelio A Teleman

Open access · bronzeAbstract read
In one paragraph

Article in Developmental cell, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 59 papers.

0numbers the graph read from it
0cells of the map it votes in
59citing papers in PubMed
4.1field-weighted citation impact, top 5% 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

59 citing papers in PubMed, 103 citations in OpenAlex.

  1. Article
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  7. Review
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  9. Article
  10. Parallel Evolution of Transcription Factors in Basal Metazoans.Methods in molecular biology (Clifton, N.J.) · 2024
    Article
  11. Article
  12. Article
  13. Article
  14. FOXO-mediated repression of Dicer1 regulates metabolism, stress resistance, and longevity inProceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  15. A novel geneeLife · 2023
    Article
  16. Article
  17. International journal of molecular sciences · 2022
    Review
  18. Article
  19. Article
  20. BMJ open diabetes research & care · 2022
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 1 institution in 1 country.

Marcel TiebeGerman Cancer Research Center (DKFZ), 69120 Heidelberg, Germany.
Marilena LutzGerman Cancer Research Center (DKFZ), 69120 Heidelberg, Germany.
Adriana De La GarzaGerman Cancer Research Center (DKFZ), 69120 Heidelberg, Germany.
Tina BuechlingDivision Signaling and Functional Genomics, German Cancer Research Center (DKFZ), 69120 Heidelberg, Germany; Department of Cell and Molecular Biology, Medical Faculty Mannheim, Heidelberg University, 69120 Heidelberg, Germany.
Michael BoutrosDivision Signaling and Functional Genomics, German Cancer Research Center (DKFZ), 69120 Heidelberg, Germany; Department of Cell and Molecular Biology, Medical Faculty Mannheim, Heidelberg University, 69120 Heidelberg, Germany.
Aurelio A TelemanGerman Cancer Research Center (DKFZ), 69120 Heidelberg, Germany. Electronic address: a.teleman@dkfz.de.
German Cancer Research Center · DE

Funding

European Research Council 260602
6 · The paper itself

Abstract

TORC1 regulates growth and metabolism, in part, by influencing transcriptional programs. Here, we identify REPTOR and REPTOR-BP as transcription factors downstream of TORC1 that are required for ∼ 90% of the transcriptional induction that occurs upon TORC1 inhibition in Drosophila. Thus, REPTOR and REPTOR-BP are major effectors of the transcriptional stress response induced upon TORC1 inhibition, analogous to the role of FOXO downstream of Akt. We find that, when TORC1 is active, it phosphorylates REPTOR on Ser527 and Ser530, leading to REPTOR cytoplasmic retention. Upon TORC1 inhibition, REPTOR becomes dephosphorylated in a PP2A-dependent manner, shuttles into the nucleus, joins its partner REPTOR-BP to bind target genes, and activates their transcription. In vivo functional analysis using knockout flies reveals that REPTOR and REPTOR-BP play critical roles in maintaining energy homeostasis and promoting animal survival upon nutrient restriction.

Indexed as

AnimalsDrosophila melanogasterDrosophila ProteinsGene Knockdown TechniquesHomeostasisMechanistic Target of Rapamycin Complex 1Multiprotein ComplexesPhosphorylationSignal TransductionTOR Serine-Threonine KinasesTranscription FactorsDrosophila ProteinsMechanistic Target of Rapamycin Complex 1Multiprotein ComplexesREPTOR-BP protein, DrosophilaREPTOR protein, DrosophilaTOR Serine-Threonine KinasesTranscription Factors

Identifiers

PMID25920570
PMCPMC4430829
OpenAlexW2150604652

What OpenQuestion holds

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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.