The core PCP protein Prickle2 regulates axon number and AIS maturation by binding to AnkG and modulating microtubule bundling

Author:

Dorrego-Rivas Ana1ORCID,Ezan Jerome1ORCID,Moreau Maïté M.1,Poirault-Chassac Sonia1,Aubailly Nathalie1,De Neve Julie1ORCID,Blanchard Camille1,Castets Francis2,Fréal Amélie3,Battefeld Arne4ORCID,Sans Nathalie1ORCID,Montcouquiol Mireille1ORCID

Affiliation:

1. Univ. Bordeaux, INSERM, Magendie, U1215, F-33077 Bordeaux, France.

2. Aix-Marseille Université, CNRS, Institut de Biologie du Développement de Marseille, UMR 7288, Case 907, 13288 Marseille Cedex 09, France.

3. Department of Functional Genomics, Vrije Universiteit (VU), Amsterdam, Netherlands.

4. Univ. Bordeaux, CNRS, IMN, UMR 5293, F-33000 Bordeaux, France.

Abstract

Core planar cell polarity (PCP) genes, which are involved in various neurodevelopmental disorders such as neural tube closure, epilepsy, and autism spectrum disorder, have poorly defined molecular signatures in neurons, mostly synapse-centric. Here, we show that the core PCP protein Prickle-like protein 2 (Prickle2) controls neuronal polarity and is a previously unidentified member of the axonal initial segment (AIS) proteome. We found that Prickle2 is present and colocalizes with AnkG480, the AIS master organizer, in the earliest stages of axonal specification and AIS formation. Furthermore, by binding to and regulating AnkG480, Prickle2 modulates its ability to bundle microtubules, a crucial mechanism for establishing neuronal polarity and AIS formation. Prickle2 depletion alters cytoskeleton organization, and Prickle2 levels determine both axon number and AIS maturation. Last, early Prickle2 depletion produces impaired action potential firing.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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