Evidence map›Paper›PMID 33021744›Full record

ArticleThe EMBO journal2020

Glycolysis regulates Hedgehog signalling via the plasma membrane potential.

Stephanie Spannl, Tomasz Buhl, Ioannis Nellas, Salma A Zeidan, K Venkatesan Iyer, Helena Khaliullina, Carsten Schultz, André Nadler, Natalie A Dye, Suzanne Eaton

Erratum issuedOpen access · hybridAbstract read
In one paragraph

Article in The EMBO journal, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.4field-weighted citation impact, top 18% 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

16 citing papers in PubMed, 26 citations in OpenAlex.

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  7. Metabolomic analysis ofbioRxiv : the preprint server for biology · 2023
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  11. Cultivation and Live Imaging of Drosophila Imaginal Discs.Methods in molecular biology (Clifton, N.J.) · 2022
    Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 4 institutions in 2 countries.

Stephanie SpannlMax Planck Institute of Molecular Cell Biology and Genetics, Dresden, Germany.ORCID 0000-0001-5999-1564
Tomasz Buhl *Max Planck Institute of Molecular Cell Biology and Genetics, Dresden, Germany.
Ioannis Nellas *Max Planck Institute of Molecular Cell Biology and Genetics, Dresden, Germany.
Salma A ZeidanMax Planck Institute of Molecular Cell Biology and Genetics, Dresden, Germany.
K Venkatesan IyerMax Planck Institute of Molecular Cell Biology and Genetics, Dresden, Germany.
Helena KhaliullinaMax Planck Institute of Molecular Cell Biology and Genetics, Dresden, Germany.
Carsten SchultzCell Biology and Biophysics Unit, European Molecular Biology Laboratory, Heidelberg, Germany.ORCID 0000-0002-5824-2171
André NadlerMax Planck Institute of Molecular Cell Biology and Genetics, Dresden, Germany.
Natalie A DyeMax Planck Institute of Molecular Cell Biology and Genetics, Dresden, Germany.ORCID 0000-0002-4859-6670
Suzanne EatonMax Planck Institute of Molecular Cell Biology and Genetics, Dresden, Germany.
Max Planck Institute of Molecular Cell Biology and Genetics · DECenter for Systems Biology Dresden · DEMax Planck Institute for the Physics of Complex Systems · DEOregon Health & Science University · US

Funding

Deutsche Forschungsgemeinschaft (DFG) SFB/TRR 83Max-Planck-Gesellschaft (MPG)
6 · The paper itself

Abstract

Changes in cell metabolism and plasma membrane potential have been linked to shifts between tissue growth and differentiation, and to developmental patterning. How such changes mediate these effects is poorly understood. Here, we use the developing wing of Drosophila to investigate the interplay between cell metabolism and a key developmental regulator-the Hedgehog (Hh) signalling pathway. We show that reducing glycolysis both lowers steady-state levels of ATP and stabilizes Smoothened (Smo), the 7-pass transmembrane protein that transduces the Hh signal. As a result, the transcription factor Cubitus interruptus accumulates in its full-length, transcription activating form. We show that glycolysis is required to maintain the plasma membrane potential and that plasma membrane depolarization blocks cellular uptake of N-acylethanolamides-lipoprotein-borne Hh pathway inhibitors required for Smo destabilization. Similarly, pharmacological inhibition of glycolysis in mammalian cells induces ciliary translocation of Smo-a key step in pathway activation-in the absence of Hh. Thus, changes in cell metabolism alter Hh signalling through their effects on plasma membrane potential.

Indexed as

AnimalsAnimals, Genetically ModifiedBiological TransportCell MembraneDrosophila melanogasterDrosophila ProteinsEnergy MetabolismGene Expression RegulationGene Expression Regulation, DevelopmentalGene Knockdown TechniquesGlycolysisGramicidinHedgehog ProteinsLipoproteinsMembrane PotentialsMembrane ProteinsDrosophila Proteinsecd protein, DrosophilaGramicidinHedgehog ProteinslipophorinLipoproteinsMembrane ProteinsSmoothened Receptorsmo protein, DrosophilaTranscription Factorsendocannabinoidsglycolysishedgehog signallingmetabolismplasma membrane potential

Identifiers

PMID33021744
PMCPMC7604625
OpenAlexW3089647356

What OpenQuestion holds

Textmetadata
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.