Evidence map›Paper›PMID 28321204›Full record

ArticleFrontiers in endocrinology2017

A Comprehensive View of the β-Arrestinome.

Pascale Crépieux, Anne Poupon, Nathalie Langonné-Gallay, Eric Reiter, Javier Delgado, Martin H Schaefer, Thomas Bourquard, Luis Serrano, Christina Kiel

Abstract read
In one paragraph

Article in Frontiers in endocrinology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
–field-weighted citation impact
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.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Review
  6. Scaffolding of Mitogen-Activated Protein Kinase Signaling by β-Arrestins.International journal of molecular sciences · 2022
    Review
  7. Article
  8. Review
  9. ERβ Regulation of Gonadotropin Responses during Folliculogenesis.International journal of molecular sciences · 2021
    Review
  10. Review
  11. Review
  12. Differential Regulation of GPCRs-Are GRK Expression Levels the Key?Frontiers in cell and developmental biology · 2021
    Review
  13. FSH for the Treatment of Male Infertility.International journal of molecular sciences · 2020
    Review
  14. GPCRomics: An Approach to Discover GPCR Drug Targets.Trends in pharmacological sciences · 2019
    Review
  15. Molecular Mechanisms of Action of FSH.Frontiers in endocrinology · 2019
    Review
  16. Review
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

9 authors.

Pascale CrépieuxINRA, UMR85, Unité Physiologie de la Reproduction et des Comportements, Nouzilly, France; «Biology and Bioinformatics of Signaling Systems (BIOS)» Group, CNRS, UMR7247, Nouzilly, France; Université François Rabelais, Tours, France; IFCE, Nouzilly, France.
Anne PouponINRA, UMR85, Unité Physiologie de la Reproduction et des Comportements, Nouzilly, France; «Biology and Bioinformatics of Signaling Systems (BIOS)» Group, CNRS, UMR7247, Nouzilly, France; Université François Rabelais, Tours, France; IFCE, Nouzilly, France.
Nathalie Langonné-GallayINRA, UMR85, Unité Physiologie de la Reproduction et des Comportements, Nouzilly, France; «Biology and Bioinformatics of Signaling Systems (BIOS)» Group, CNRS, UMR7247, Nouzilly, France; Université François Rabelais, Tours, France; IFCE, Nouzilly, France.
Eric ReiterINRA, UMR85, Unité Physiologie de la Reproduction et des Comportements, Nouzilly, France; «Biology and Bioinformatics of Signaling Systems (BIOS)» Group, CNRS, UMR7247, Nouzilly, France; Université François Rabelais, Tours, France; IFCE, Nouzilly, France.
Javier DelgadoEMBL/CRG Systems Biology Research Unit, Centre for Genomic Regulation (CRG), Barcelona Institute of Science and Technology, Barcelona, Spain; Universitat Pompeu Fabra (UPF), Barcelona, Spain.
Martin H SchaeferEMBL/CRG Systems Biology Research Unit, Centre for Genomic Regulation (CRG), Barcelona Institute of Science and Technology, Barcelona, Spain; Universitat Pompeu Fabra (UPF), Barcelona, Spain.
Thomas BourquardINRA, UMR85, Unité Physiologie de la Reproduction et des Comportements, Nouzilly, France; «Biology and Bioinformatics of Signaling Systems (BIOS)» Group, CNRS, UMR7247, Nouzilly, France; Université François Rabelais, Tours, France; IFCE, Nouzilly, France.
Luis SerranoEMBL/CRG Systems Biology Research Unit, Centre for Genomic Regulation (CRG), Barcelona Institute of Science and Technology, Barcelona, Spain; Universitat Pompeu Fabra (UPF), Barcelona, Spain; Institució Catalana de Recerca i Estudis Avançats, Barcelona, Spain.
Christina KielEMBL/CRG Systems Biology Research Unit, Centre for Genomic Regulation (CRG), Barcelona Institute of Science and Technology, Barcelona, Spain; Universitat Pompeu Fabra (UPF), Barcelona, Spain.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

G protein-coupled receptors (GPCRs) are membrane receptors critically involved in sensing the environment and orchestrating physiological processes. As such, they transduce extracellular signals such as hormone, neurotransmitters, ions, and light into an integrated cell response. The intracellular trafficking, internalization, and signaling ability of ligand-activated GPCRs are controlled by arrestins, adaptor proteins that they interact with upon ligand binding. β-arrestins 1 and 2 in particular are now considered as hub proteins assembling multiprotein complexes to regulate receptor fate and transduce diversified cell responses. While more than 400 β-arrestin interaction partners have been identified so far, much remains to be learnt on how discrimination between so many binding partners is accomplished. Here, we gathered the interacting partners of β-arrestins through database mining and manual curation of the literature to map the β-arrestin interactome (β-arrestinome). We discussed several parameters that determine compatible (AND) or mutually exclusive (XOR) binding of β-arrestin interactors, such as structural constraints, intracellular abundance, or binding affinity.

Indexed as

G protein-coupled receptorshub proteinsprotein/protein interaction networksystems biologyβ-arrestins

Identifiers

PMID28321204
PMCPMC5337525

What OpenQuestion holds

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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.