| Literature DB >> 33627667 |
Huijie Zhao1,2, Qingxia Chen1,3, Fan Li1,2, Lihong Cui4, Lele Xie1, Qiongping Huang1, Xin Liang4, Jun Zhou5, Xiumin Yan6, Xueliang Zhu7,8,9,10.
Abstract
Multicilia are delicate motile machineries, and how they are accurately assembled is poorly understood. Here, we show that fibrogranular materials (FGMs), large arrays of electron-dense granules specific to multiciliated cells, are essential for their ultrastructural fidelity. Pcm1 forms the granular units that further network into widespread FGMs, which are abundant in spherical FGM cores. FGM cores selectively concentrate multiple important centriole-related proteins as clients, including Cep131 that specifically decorates a foot region of ciliary central pair (CP) microtubules. FGMs also tightly contact deuterosome-procentriole complexes. Disruption of FGMs in mouse cells undergoing multiciliogenesis by Pcm1 RNAi markedly deregulates centriolar targeting of FGM clients, elongates CP-foot, and alters deuterosome size, number, and distribution. Although the multicilia are produced in correct numbers, they display abnormal ultrastructure and motility. Our results suggest that FGMs organize deuterosomes and centriole-related proteins to facilitate the faithful assembly of basal bodies and multiciliary axonemes.Entities:
Year: 2021 PMID: 33627667 DOI: 10.1038/s41467-021-21506-8
Source DB: PubMed Journal: Nat Commun ISSN: 2041-1723 Impact factor: 14.919