4.7 Article

CFEOM1-Associated Kinesin KIF21A Is a Cortical Microtubule Growth Inhibitor

期刊

DEVELOPMENTAL CELL
卷 27, 期 2, 页码 145-160

出版社

CELL PRESS
DOI: 10.1016/j.devcel.2013.09.010

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资金

  1. Human Frontier Science Program
  2. Fondation pour la Recherche Medicale (FRM, France)
  3. Marie-Curie Intra-European Fellowship for career development
  4. Netherlands Organization for Scientific Research ALW open program
  5. Erasmus MC
  6. ALW-VICI
  7. ZonMw-VIDI
  8. European Science Foundation
  9. Center for Translational Molecular Medicine (CTMM) [01C-204]

向作者/读者索取更多资源

Mechanisms controlling microtubule dynamics at the cell cortex play a crucial role in cell morphogenesis and neuronal development. Here, we identified kinesin-4 KIF21A as an inhibitor of microtubule growth at the cell cortex. In vitro, KIF21A suppresses microtubule growth and inhibits catastrophes. In cells, KIF21A restricts microtubule growth and participates in organizing microtubule arrays at the cell edge. KIF21A is recruited to the cortex by KANK1, which coclusters with liprin-alpha 1/beta 1 and the components of the LL5 beta-containing cortical microtubule attachment complexes. Mutations in KIF21A have been linked to congenital fibrosis of the extraocular muscles type 1 (CFEOM1), a dominant disorder associated with neurodevelopmental defects. CFEOM1-associated mutations relieve autoinhibition of the KIF21A motor, and this results in enhanced KIF21A accumulation in axonal growth cones, aberrant axon morphology, and reduced responsiveness to inhibitory cues. Our study provides mechanistic insight into cortical microtubule regulation and suggests that altered microtubule dynamics contribute to CFEOM1 pathogenesis.

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