Nuclear-cytoplasmic translocation of MCIDAS couples transcription with massive de novo centriole biogenesis in multiciliated cells. Lu H, Goh KJ, Tan EK, James CT, Ghosh A, Boudjema AR, Lorenzini PA, Bingle CD, Maurer-Stroh S, Biswas NK, Meunier A, Dunn NR, Roy S. Cell Rep. 2025 Oct 28;44(10):116321. doi: 10.1016/j.celrep.2025.116321. Epub 2025 Sep 19. PMID: 40974574.
Abstract
Multiciliated cells (MCCs) bear numerous motile cilia that drive fluid flow, but how numerous centrioles for multiciliation are generated has remained unresolved. Here, we report that the "master" MCC transcriptional regulator, MCIDAS, moonlights in the cytoplasm to organize massive centriole biogenesis. Like MCIDAS, its co-transcriptional factors, E2F4 and E2F5, also undergo cytoplasmic accumulation, colocalizing with MCIDAS and forming procentrioles. MCIDAS loss inhibited E2F4/5 cytoplasmic accumulation and blocked centriole assembly. Furthermore, we show that the cytoplasmic accumulation of MCIDAS is mediated by CRM1-dependant nuclear export, and its inhibition specifically compromised centriole biogenesis. By contrast, on loss of parental centrioles and deuterosomes, which does not impair centriole formation, E2F4 cytoplasmic localization remained unaffected, establishing that the MCIDAS-E2F4/5 cytoplasmic complex represents the de novo centriole biogenesis pathway. We have also assembled a comprehensive list of MCIDAS targets, a resource which will enable further exposition of MCC biology and pathological mechanisms of motile ciliopathies.
