Evidence map›Paper›PMID 37656621›Full record

ArticleCell reports2023

System-wide mapping of peptide-GPCR interactions in C. elegans.

Isabel Beets, Sven Zels, Elke Vandewyer, Jonas Demeulemeester, Jelle Caers, Esra Baytemur, Amy Courtney, Luca Golinelli, İlayda Hasakioğulları, William R Schafer and 3 more

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 73 papers.

0numbers the graph read from it
0cells of the map it votes in
73citing papers in PubMed
16.5field-weighted citation impact, top 1% 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

73 citing papers in PubMed, 111 citations in OpenAlex.

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13 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

13 authors at 5 institutions in 3 countries.

Isabel BeetsDepartment of Biology, KU Leuven, 3000 Leuven, Belgium. Electronic address: isabel.beets@kuleuven.be.
Sven ZelsDepartment of Biology, KU Leuven, 3000 Leuven, Belgium.
Elke VandewyerDepartment of Biology, KU Leuven, 3000 Leuven, Belgium.
Jonas DemeulemeesterThe Francis Crick Institute, London NW1 1AT, UK; VIB - KU Leuven Center for Cancer Biology, 3000 Leuven, Belgium; Department of Oncology, KU Leuven, 3000 Leuven, Belgium.
Jelle CaersDepartment of Biology, KU Leuven, 3000 Leuven, Belgium.
Esra BaytemurDepartment of Biology, KU Leuven, 3000 Leuven, Belgium.
Amy CourtneyNeurobiology Division, MRC Laboratory of Molecular Biology, Cambridge CB2 0QH, UK.
Luca GolinelliDepartment of Biology, KU Leuven, 3000 Leuven, Belgium.
İlayda HasakioğullarıDepartment of Biology, KU Leuven, 3000 Leuven, Belgium.
William R SchaferNeurobiology Division, MRC Laboratory of Molecular Biology, Cambridge CB2 0QH, UK.
Petra E VértesDepartment of Psychiatry, Behavioural and Clinical Neuroscience Institute, University of Cambridge, Cambridge CB2 3EB, UK.
Olivier MirabeauInstitut Pasteur, Université Paris Cité, Bioinformatics and Biostatistics Hub, Inserm U1224, Brain-Immune Communication Lab, 75015 Paris, France.
Liliane SchoofsDepartment of Biology, KU Leuven, 3000 Leuven, Belgium.
KU Leuven · BEMRC Laboratory of Molecular Biology · GBInserm · FRThe Francis Crick Institute · GBUniversity of Cambridge · GB

Funding

The neuropeptidergic connectome of Caenorhabitis elegantR01NS110391 · NINDS · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI BEETS, ISABEL, HOBERT, OLIVER · 2018 to 2021
$2.0M
Medical Research Council MC_U105185857NINDS NIH HHS R01 NS110391
6 · The paper itself

Abstract

Neuropeptides and peptide hormones are ancient, widespread signaling molecules that underpin almost all brain functions. They constitute a broad ligand-receptor network, mainly by binding to G protein-coupled receptors (GPCRs). However, the organization of the peptidergic network and roles of many peptides remain elusive, as our insight into peptide-receptor interactions is limited and many peptide GPCRs are still orphan receptors. Here we report a genome-wide peptide-GPCR interaction map in Caenorhabditis elegans. By reverse pharmacology screening of over 55,384 possible interactions, we identify 461 cognate peptide-GPCR couples that uncover a broad signaling network with specific and complex combinatorial interactions encoded across and within single peptidergic genes. These interactions provide insights into peptide functions and evolution. Combining our dataset with phylogenetic analysis supports peptide-receptor co-evolution and conservation of at least 14 bilaterian peptidergic systems in C. elegans. This resource lays a foundation for system-wide analysis of the peptidergic network.

Indexed as

NeuropeptidesPeptide HormonesAnimalsCaenorhabditis elegansPhylogenyReceptors, G-Protein-CoupledNeuropeptidesPeptide HormonesReceptors, G-Protein-CoupledC. elegansCP: Cell biologyCP: NeuroscienceGPCRinteractomeneuropeptidereverse pharmacology

Identifiers

PMID37656621
PMCPMC7615250
OpenAlexW4386315668

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.