4.8 Article

CDKL kinase regulates the length of the ciliary proximal segment

Journal

CURRENT BIOLOGY
Volume 31, Issue 11, Pages 2359-+

Publisher

CELL PRESS
DOI: 10.1016/j.cub.2021.03.068

Keywords

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Funding

  1. Canadian Institutes of Health Research (CIHR) [MOP-142243, PJT-156042]
  2. Vanier Canada Graduate Scholarship
  3. Michael Smith Foundation for Health Research (MSFHR) senior scholar award
  4. Science Foundation Ireland (SFI)
  5. Biotechnology and Biological Sciences Research Council (BBSRC) [16/BBSRC/3394]
  6. Science Foundation Ireland (SFI) [16/BBSRC/3394] Funding Source: Science Foundation Ireland (SFI)

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Cilia play essential roles in cell motility, fluid flow, and signaling, and are divided into subcompartments with variable structures and functions. CDKL-1, a kinase related to the human CDKL family, controls the length of a specific ciliary subdomain and influences cilium-dependent processes. Overall, cilium length is regulated by various pathways and CDKL-1 is crucial for the construction of a specific ciliary compartment and contributes to development and sensory physiology.
Cilia are organelles found throughout most unicellular eukaryotes and different metazoan cell types. To accomplish their essential roles in cell motility, fluid flow, and signaling, cilia are divided into subcompartments with variable structures, compositions, and functions. How these specific subcompartments are built remains almost completely unexplored. Here, we show that C. elegans CDKL-1, related to the human CDKL kinase family (CDKL1/CDKL2/CDKL3/CDKL4/CDKL5), specifically controls the length of the proximal segment, a ciliary subdomain conserved in evolution from Tetrahymena motile cilia to C. elegans chemosensory, mammalian olfactory, and photoreceptor non-motile cilia. CDKL-1 associates with intraflagellar transport (IFT), influences the distribution of the IFT anterograde motors heterotrimeric kinesin-II and homodimeric OSM-3-kinesin/KIF17 in the proximal segment, and shifts the boundary between the proximal and distal segments (PS/DS boundary). CDKL-1 appears to function independently from several factors that influence cilium length, namely the kinases DYF-5 (mammalian CILK1/MAK) and NEKL-1 (NEK9), as well as the depolymerizing kinesins KLP-13 (KIF19) and KLP-7 (KIF2). However, a different kinase, DYF-18 (CCRK), is needed for the correct localization and function of CDKL-1 and similarly influences the length of the proximal segment. Loss of CDKL-1, which affects proximal segment length without impairing overall ciliary microtubule structural integrity, also impairs cilium-dependent processes, namely cGMP-signaling-dependent body length control and CO2 avoidance. Collectively, our findings suggest that cilium length is regulated by various pathways and that the IFT-associated kinase CDKL-1 is essential for the construction of a specific ciliary compartment and contributes to development and sensory physiology.

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