PUBLICATION
Mcidas mutant mice reveal a two-step process for the specification and differentiation of multiciliated cells in mammals
- Authors
- Lu, H., Anujan, P., Zhou, F., Zhang, Y., Chong, Y.L., Bingle, C.D., Roy, S.
- ID
- ZDB-PUB-200108-27
- Date
- 2019
- Source
- Development (Cambridge, England) 146(6): (Journal)
- Registered Authors
- Roy, Sudipto
- Keywords
- Cilia, Deuterosome, E2F, GMNC, MCIDAS, Multiciliated cell
- MeSH Terms
-
- Animals
- Basal Bodies/physiology
- Carrier Proteins/physiology
- Cell Cycle Proteins/genetics
- Cell Cycle Proteins/physiology*
- Cell Differentiation
- Cell Nucleus/physiology
- Cilia/physiology*
- Ciliopathies
- Gene Expression Regulation, Developmental
- HEK293 Cells
- Humans
- Mice
- Mice, Inbred C57BL
- Mice, Knockout
- Mice, Mutant Strains*
- Nuclear Proteins/genetics
- Nuclear Proteins/physiology*
- Protein Domains
- Zebrafish
- PubMed
- 30877126 Full text @ Development
Citation
Lu, H., Anujan, P., Zhou, F., Zhang, Y., Chong, Y.L., Bingle, C.D., Roy, S. (2019) Mcidas mutant mice reveal a two-step process for the specification and differentiation of multiciliated cells in mammals. Development (Cambridge, England). 146(6):.
Abstract
Motile cilia on multiciliated cells (MCCs) function in fluid clearance over epithelia. Studies with Xenopus embryos and individuals with the congenital respiratory disorder reduced generation of multiple motile cilia (RGMC), have implicated the nuclear protein MCIDAS (MCI), in the transcriptional regulation of MCC specification and differentiation. Recently, a paralogous protein, geminin coiled-coil domain containing (GMNC), was also shown to be required for MCC formation. Surprisingly, in contrast to the presently held view, we find that Mci mutant mice can specify MCC precursors. However, these precursors cannot produce multiple basal bodies, and mature into single ciliated cells. We identify an essential role for MCI in inducing deuterosome pathway components for the production of multiple basal bodies. Moreover, GMNC and MCI associate differentially with the cell-cycle regulators E2F4 and E2F5, which enables them to activate distinct sets of target genes (ciliary transcription factor genes versus basal body amplification genes). Our data establish a previously unrecognized two-step model for MCC development: GMNC functions in the initial step for MCC precursor specification. GMNC induces Mci expression that drives the second step of basal body production for multiciliation.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping