A role for Cep70 in centriole amplification in multiciliated cells

Sun Kim (1) , Eva Brotslaw (1) , Virginie Thome (2) , Jen Mitchell (1) , Rosa Ventrella (1) , Caitlin Collins (1) , Brian Mitchell (1)

1 Department of Cell and Developmental Biology, Lurie Comprehensive Cancer Center, Northwestern University, Feinberg School of Medicine
2 IBDM - Institut de Biologie du Développement de Marseille

Centriole amplification in multiciliated cells occurs in a pseudo-cell cycle regulated process that typically utilizes a poorly characterized molecularly dense structure called the deuterosome. We identified the centrosomal protein Cep70 as a novel deuterosome-associated protein that forms a complex with other deuterosome proteins, CCDC78 and Deup1. Cep70 dynamically associates with deuterosomes during centriole amplification in the ciliated epithelia of Xenopus embryos. Cep70 is not found in nascent deuterosomes prior to amplification. However, it becomes localized at deuterosomes at the onset of centriole biogenesis and remains there after the completion of centriole amplification. Deuterosome localization requires a conserved C-terminal "Cep70" motif. Depletion of Cep70 using morpholino oligos or CRISPR/Cas9 editing in F0 embryos leads to a severe decrease in centriole formation in both endogenous MCCs, as well as ectopically induced MCCs. Consistent with a decrease in centrioles, endogenous MCCs have defects in the process of radial intercalation. We propose that Cep70 represents a novel regulator of centriole biogenesis in MCCs.

Mots clés: Multiciliated cell; Cep70; Deuterosome; Centriole amplification; Radial intercalation

Domaines: Sciences du Vivant [q-bio]

Sun Kim, Eva Brotslaw, Virginie Thome, Jen Mitchell, Rosa Ventrella, et al.. A role for Cep70 in centriole amplification in multiciliated cells. Developmental Biology, 2021, 471, pp.10-17. ⟨10.1016/j.ydbio.2020.11.011⟩. ⟨hal-03590986⟩