CEP164C regulates flagellum length in stable flagella

Author:

Atkins Madison1,Týč Jiří1ORCID,Shafiq Shahaan1,Ahmed Manu1,Bertiaux Eloïse23,De Castro Neto Artur Leonel1,Sunter Jack1ORCID,Bastin Philippe2ORCID,Dean Samuel Dale4ORCID,Vaughan Sue1ORCID

Affiliation:

1. Biological and Medical Sciences, Oxford Brookes University, Oxford, UK

2. Trypanosome Cell Biology Unit and Institut National de la Santé et de la Recherche Médicale U1201, Institut Pasteur, Paris, France

3. Sorbonne Université école doctorale complexité du vivant, Paris, France

4. Warwick Medical School, University of Warwick, Coventry, UK

Abstract

Cilia and flagella are required for cell motility and sensing the external environment and can vary in both length and stability. Stable flagella maintain their length without shortening and lengthening and are proposed to “lock” at the end of growth, but molecular mechanisms for this lock are unknown. We show that CEP164C contributes to the locking mechanism at the base of the flagellum in Trypanosoma brucei. CEP164C localizes to mature basal bodies of fully assembled old flagella, but not to growing new flagella, and basal bodies only acquire CEP164C in the third cell cycle after initial assembly. Depletion of CEP164C leads to dysregulation of flagellum growth, with continued growth of the old flagellum, consistent with defects in a flagellum locking mechanism. Inhibiting cytokinesis results in CEP164C acquisition on the new flagellum once it reaches the old flagellum length. These results provide the first insight into the molecular mechanisms regulating flagella growth in cells that must maintain existing flagella while growing new flagella.

Funder

Biotechnology and Biological Sciences Research Council

Wellcome Trust

Institut Pasteur

La Fondation pour la Recherche Médicale

Publisher

Rockefeller University Press

Subject

Cell Biology

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