EFA6A, an exchange factor for Arf6, regulates early steps in ciliogenesis.


Journal

Journal of cell science
ISSN: 1477-9137
Titre abrégé: J Cell Sci
Pays: England
ID NLM: 0052457

Informations de publication

Date de publication:
22 01 2021
Historique:
received: 28 05 2020
accepted: 20 11 2020
entrez: 23 1 2021
pubmed: 24 1 2021
medline: 22 6 2021
Statut: epublish

Résumé

Ciliogenesis is a coordinated process initiated by the recruitment and fusion of pre-ciliary vesicles at the distal appendages of the mother centriole through mechanisms that remain unclear. Here, we report that EFA6A (also known as PSD), an exchange factor for the small G protein Arf6, is involved in early stage of ciliogenesis by promoting the fusion of distal appendage vesicles forming the ciliary vesicle. EFA6A is present in the vicinity of the mother centriole before primary cilium assembly and prior to the arrival of Arl13B-containing vesicles. During ciliogenesis, EFA6A initially accumulates at the mother centriole and later colocalizes with Arl13B along the ciliary membrane. EFA6A depletion leads to the inhibition of ciliogenesis, the absence of centrosomal Rab8-positive structures and the accumulation of Arl13B-positive vesicles around the distal appendages. Our results uncover a novel fusion machinery, comprising EFA6A, Arf6 and Arl13B, that controls the coordinated fusion of ciliary vesicles docked at the distal appendages of the mother centriole.

Identifiants

pubmed: 33483367
pii: 237326
doi: 10.1242/jcs.249565
pii:
doi:

Substances chimiques

Guanine Nucleotide Exchange Factors 0
ADP-Ribosylation Factors EC 3.6.5.2

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© 2021. Published by The Company of Biologists Ltd.

Déclaration de conflit d'intérêts

Competing interestsThe authors declare no competing or financial interests.

Auteurs

Mariagrazia Partisani (M)

Institut de Pharmacologie Moléculaire et Cellulaire (IPMC), UMR 7275 CNRS-Université Côte d'Azur, 660, route des lucioles, 06560 Valbonne, France.

Carole L Baron (CL)

Institut de Pharmacologie Moléculaire et Cellulaire (IPMC), UMR 7275 CNRS-Université Côte d'Azur, 660, route des lucioles, 06560 Valbonne, France.

Rania Ghossoub (R)

Centre de Recherche en Cancérologie de Marseille (CRCM), Inserm, U1068-CNRS UMR7258, Aix-Marseille Université, Institut Paoli-Calmettes, 13009 Marseille, France.

Racha Fayad (R)

Institut de Pharmacologie Moléculaire et Cellulaire (IPMC), UMR 7275 CNRS-Université Côte d'Azur, 660, route des lucioles, 06560 Valbonne, France.

Sophie Pagnotta (S)

Centre Commun de Microscopie Appliquée (CCMA), Université Côte d'Azur Parc Valrose, 06103 Nice cedex 2, France.

Sophie Abélanet (S)

Institut de Pharmacologie Moléculaire et Cellulaire (IPMC), UMR 7275 CNRS-Université Côte d'Azur, 660, route des lucioles, 06560 Valbonne, France.

Eric Macia (E)

Institut de Pharmacologie Moléculaire et Cellulaire (IPMC), UMR 7275 CNRS-Université Côte d'Azur, 660, route des lucioles, 06560 Valbonne, France.

Frédéric Brau (F)

Institut de Pharmacologie Moléculaire et Cellulaire (IPMC), UMR 7275 CNRS-Université Côte d'Azur, 660, route des lucioles, 06560 Valbonne, France.

Sandra Lacas-Gervais (S)

Centre Commun de Microscopie Appliquée (CCMA), Université Côte d'Azur Parc Valrose, 06103 Nice cedex 2, France.

Alexandre Benmerah (A)

Université de Paris, Imagine Institute, Laboratory of Inherited Kidney Diseases, INSERM UMR 1163, F-75015, Paris, France.

Frédéric Luton (F)

Institut de Pharmacologie Moléculaire et Cellulaire (IPMC), UMR 7275 CNRS-Université Côte d'Azur, 660, route des lucioles, 06560 Valbonne, France.

Michel Franco (M)

Institut de Pharmacologie Moléculaire et Cellulaire (IPMC), UMR 7275 CNRS-Université Côte d'Azur, 660, route des lucioles, 06560 Valbonne, France franco@ipmc.cnrs.fr.

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Classifications MeSH