Dzip1 and Fam92 form a ciliary transition zone complex with cell type specific roles in Drosophila

Author:

Lapart Jean-André1ORCID,Gottardo Marco2,Cortier Elisabeth1,Duteyrat Jean-Luc1,Augière Céline1,Mangé Alain3ORCID,Jerber Julie1,Solassol Jérôme3,Gopalakrishnan Jay2,Thomas Joëlle1ORCID,Durand Bénédicte1ORCID

Affiliation:

1. Institut NeuroMyoGène, CNRS UMR 5310, INSERM U1217, Université Claude Bernard Lyon 1, Lyon, France

2. Institute of Human Genetics, Universitätsklinikum Düsseldorf, Heinrich-Heine-Universität Düsseldorf, Düsseldorf, Germany

3. IRCM, INSERM, Université de Montpellier, ICM, Montpellier, France

Abstract

Cilia and flagella are conserved eukaryotic organelles essential for cellular signaling and motility. Cilia dysfunctions cause life-threatening ciliopathies, many of which are due to defects in the transition zone (TZ), a complex structure of the ciliary base. Therefore, understanding TZ assembly, which relies on ordered interactions of multiprotein modules, is of critical importance. Here, we show that Drosophila Dzip1 and Fam92 form a functional module which constrains the conserved core TZ protein, Cep290, to the ciliary base. We identify cell type specific roles of this functional module in two different tissues. While it is required for TZ assembly in all Drosophila ciliated cells, it also regulates basal-body growth and docking to the plasma membrane during spermatogenesis. We therefore demonstrate a novel regulatory role for Dzip1 and Fam92 in mediating membrane/basal-body interactions and show that these interactions exhibit cell type specific functions in basal-body maturation and TZ organization.

Funder

Agence Nationale de la Recherche

Fondation pour la Recherche Médicale

Université Claude Bernard Lyon 1

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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