Aug 2026· Nature Communications· Vol 17· 0 citations· 56 references
Medicine
TL;DR
An important role is identified for cilia and flagella associated protein 100 (CFAP100) in the transition zone assembly of the ciliary transition zone, providing insights into the physicochemical principle governing ciliogenesis.
Abstract
Cilia are microtubule-based cellular protrusions critical for cell signaling and motility. The ciliary transition zone connects axonemal microtubules to the ciliary membrane and functions as a gatekeeper by regulating selective targeting and sorting of proteins. However, the molecular mechanisms underlying its assembly remain incompletely understood. Herein, we identify an important role for cilia and flagella associated protein 100 (CFAP100) in the transition zone assembly. Cfap100 knockout mice exhibit ciliary defects in multiple organs, including the brain, trachea, and kidney. Super-resolution imaging reveals that CFAP100 forms a ring-like structure at the distal end of centrioles. Molecular analyses demonstrate that CFAP100 stimulates the transition zone assembly and interacts with nephrocystin-3 (NPHP3), a component of the inversin compartment that localizes adjacent to the transition zone. Further investigation shows that CFAP100 contains an intrinsically disordered region and forms dynamic biomolecular condensates during ciliogenesis, which are sufficient to promote transition zone assembly. Moreover, the phase separation capacity of CFAP100 correlates with its ability to recruit NPHP3. Together, our findings reveal a mechanism through which CFAP100 phase separation promotes ciliary transition zone assembly, providing insights into the physicochemical principle governing ciliogenesis. Here they identify CFAP100 as a critical regulator of ciliary transition zone assembly. Mechanistically, CFAP100 forms phase-separated condensates that promote transition zone organization, and recruits NPHP3 to facilitate ciliogenesis.
The basal body (BB) is essential for axoneme assembly and ciliary function, and its defects are associated with ciliogenesis disorders and ciliopathies1,2. However, the molecular basis of the BB’s region-specific transitions along the proximal-distal axis, and the mechanism by which ciliary central pair (CP) microtubul...
Zi-Yang Wang, Huan Yang, Hao Lang et al.· bioRxiv· 0 citations
How microtubule (MT) growth is locally sustained within cilia remains a central unanswered question in ciliogenesis. Here we identify RAT-1 as a regulator of ciliary tubulin homeostasis and MT growth. Genetic screens in Caenorhabditis elegans show that loss of RAT-1 suppresses the toxic effects of a mutant α-tubulin an...
A three-dimensional ultrastructural analysis reveals previously unrecognized intermediate stages in the formation of primary cilia and identifies the endocytotic protein GRAF1 as being essential during the early stages of ciliogenesis and for the delivery of plasma membrane-derived material to the developing ciliary me...
Kerstin N. Schmidt, Korbinian Buerger, Olga Maier et al.· Nature Communications· 0 citations
These findings uncover a conserved mechanism of B-tubule initiation and underscore the necessity for spatially restricted expression of MTD assembly factors during ciliogenesis.
Ming Li, Guang-Han Chen, Zhe Chen et al.· Proceedings of the National...· 0 citations
Ciliary shortening disrupts cilium-dependent signaling and tissue homeostasis and contributes to diverse ciliopathies and acquired disorders. However, the underlying mechanisms and pharmacological strategies for restoring ciliary length remain poorly understood. Here, we identify Kaempferol (Kae) as a previously unreco...
Xu-Yao Dai, Yi Zhao, Ruo-Dan Xu et al.· Cells· 0 citations
We use cookies to run the site and, with your consent, for analytics and to show ads.
See our Cookie Policy.