The MIR34B/C genomic region contains multiple potential regulators of multiciliogenesis

Author:

Cavard Amélie1,Redman Elisa1,Mercey Olivier2,Abelanet Sophie1,Plaisant Magali1,Arguel Marie‐Jeanne1,Magnone Virginie1,Ruiz García Sandra1,Rios Géraldine1,Deprez Marie1,Lebrigand Kévin1,Ponzio Gilles1,Caballero Ignacio3,Barbry Pascal1,Zaragosi Laure‐Emmanuelle1ORCID,Marcet Brice1

Affiliation:

1. Université Côte d'Azur, CNRS, IPMC Sophia‐Antipolis France

2. Institut de Biologie de l'École Normale Supérieure Paris France

3. ISP, INRA, Université Tours Nouzilly France

Abstract

The MIR449 genomic locus encompasses several regulators of multiciliated cell (MCC) formation (multiciliogenesis). The miR‐449 homologs miR‐34b/c represent additional regulators of multiciliogenesis that are transcribed from another locus. Here, we characterized the expression of BTG4, LAYN, and HOATZ, located in the MIR34B/C locus using single‐cell RNA‐seq and super‐resolution microscopy from human, mouse, or pig multiciliogenesis models. BTG4, LAYN, and HOATZ transcripts were expressed in both precursors and mature MCCs. The Layilin/LAYN protein was absent from primary cilia, but it was expressed in apical membrane regions or throughout motile cilia. LAYN silencing altered apical actin cap formation and multiciliogenesis. HOATZ protein was detected in primary cilia or throughout motile cilia. Altogether, our data suggest that the MIR34B/C locus may gather potential actors of multiciliogenesis.

Funder

Agence Nationale de la Recherche

Association Vaincre la Mucoviscidose

Canceropôle PACA

Chan Zuckerberg Initiative

Fondation ARC pour la Recherche sur le Cancer

Fondation pour la Recherche Médicale

H2020 Health

Ligue Contre le Cancer

Silicon Valley Community Foundation

Publisher

Wiley

Subject

Cell Biology,Genetics,Molecular Biology,Biochemistry,Structural Biology,Biophysics

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