High hedgehog signaling is transduced by a multikinase-dependent switch controlling the apico-basal distribution of the GPCR smoothened.


Journal

eLife
ISSN: 2050-084X
Titre abrégé: Elife
Pays: England
ID NLM: 101579614

Informations de publication

Date de publication:
09 09 2022
Historique:
received: 29 04 2022
accepted: 22 08 2022
entrez: 9 9 2022
pubmed: 10 9 2022
medline: 14 9 2022
Statut: epublish

Résumé

The oncogenic G-protein-coupled receptor (GPCR) Smoothened (SMO) is a key transducer of the hedgehog (HH) morphogen, which plays an essential role in the patterning of epithelial structures. Here, we examine how HH controls SMO subcellular localization and activity in a polarized epithelium using the

Identifiants

pubmed: 36083801
doi: 10.7554/eLife.79843
pii: 79843
pmc: PMC9462849
doi:
pii:

Substances chimiques

Drosophila Proteins 0
Hedgehog Proteins 0
Receptors, G-Protein-Coupled 0
Smoothened Receptor 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© 2022, Gonçalves Antunes et al.

Déclaration de conflit d'intérêts

MG, MS, VC, SC, AP, IB No competing interests declared

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Auteurs

Marina Gonçalves Antunes (M)

Université Paris Cité, CNRS, Institut Jacques Monod, Paris, France.

Matthieu Sanial (M)

Université Paris Cité, CNRS, Institut Jacques Monod, Paris, France.

Vincent Contremoulins (V)

Université Paris Cité, CNRS, Institut Jacques Monod, Paris, France.

Sandra Carvalho (S)

Université Paris Cité, CNRS, Institut Jacques Monod, Paris, France.

Anne Plessis (A)

Université Paris Cité, CNRS, Institut Jacques Monod, Paris, France.

Isabelle Becam (I)

Université Paris Cité, CNRS, Institut Jacques Monod, Paris, France.

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Classifications MeSH