4.8 Article

Balancing the length of the distal tip by septins is key for stability and signalling function of primary cilia

期刊

EMBO JOURNAL
卷 41, 期 1, 页码 -

出版社

WILEY
DOI: 10.15252/embj.2021108843

关键词

cilia length; segmentation; KIF7; septins; sonic hedgehog signalling; transition zone

资金

  1. Heidelberg Biosciences International Graduate School (HBIGS)
  2. Deutsche Forschungsgemeinschaft (DFG) [SFB873]
  3. Deutsche Forschungsgemeinschaft Heisenberg Professorship [PE1883/3, PE1883/4]
  4. Cluster of Excellence 3DMM2O [EXC-2082/1-390761711]
  5. Projekt DEAL

向作者/读者索取更多资源

Understanding the segmentation of primary cilia is important for controlling their length and signaling functions. Perturbations leading to cilia over-elongation have been shown to impact different segments of the cilia axonemes, influencing cilia behavior. Septins have been identified as novel repressors of distal segment (DS) growth.
Primary cilia are antenna-like organelles required for signalling transduction. How cilia structure is mechanistically maintained at steady-state to promote signalling is largely unknown. Here, we define that mammalian primary cilia axonemes are formed by proximal segment (PS) and distal segment (DS) delineated by tubulin polyglutamylation-rich and -poor regions, respectively. The analysis of proximal/distal segmentation indicated that perturbations leading to cilia over-elongation influenced PS or DS length with a different impact on cilia behaviour. We identified septins as novel repressors of DS growth. We show that septins control the localisation of MKS3 and CEP290 required for a functional transition zone (TZ), and the cilia tip accumulation of the microtubule-capping kinesin KIF7, a cilia-growth inhibitor. Live-cell imaging and analysis of sonic-hedgehog (SHH) signalling activation established that DS over-extension increased cilia ectocytosis events and decreased SHH activation. Our data underlines the importance of understanding cilia segmentation for length control and cilia-dependent signalling.

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