@article {34236,
	title = {GemC1 controls multiciliogenesis in the airway epithelium},
	journal = {*Equal contribution. EMBO reports},
	volume = {17},
	year = {2016},
	pages = {400-413},
	abstract = {Multiciliated cells are terminally differentiated, post-mitotic cells that form hundreds of motile cilia on their apical surface. Defects in multiciliated cells lead to disease, including mucociliary clearance disorders that result from ciliated cell disfunction in airways. The pathway controlling multiciliogenesis, however, remains poorly characterized. We showed that GemC1, previously implicated in cell cycle control, is a central regulator of ciliogenesis. GemC1 is specifically expressed in ciliated epithelia. Ectopic expression of GemC1 is sufficient to induce early steps of multiciliogenesis in airway epithelial cells ex vivo, upregulating McIdas and FoxJ1, key transcriptional regulators of multiciliogenesis. GemC1 directly transactivates the McIdas and FoxJ1 upstream regulatory sequences, and its activity is enhanced by E2F5 and inhibited by Geminin. GemC1-knockout mice are born with airway epithelia devoid of multiciliated cells. Our results identify GemC1 as an essential regulator of ciliogenesis in the airway epithelium and a candidate gene for mucociliary disorders.},
	isbn = {1469-221X},
	url = {https://pubmed.ncbi.nlm.nih.gov/26882546/},
	author = {Arbi, Marina and Pefani, Dafni-Eleftheria* and Kyrousi, Christina* and Lalioti, Maria-Eleni and Kalogeropoulou, Argyro and Papanastasiou, Anastasios D and Taraviras, Stavros and Lygerou, Zoi}
}
