Science SignalingNeurosciencePeer-reviewed journal article
Neurodevelopmental disorder associated mutations in TAOK1 reveal its function as a plasma membrane remodeling kinase
Abstract
Mutations in TAOK1, a serine-threonine kinase encoding gene are strongly associated with both autism spectrum disorder (ASD) and neurodevelopmental delay (NDD). However, molecular function of this evolutionarily conserved kinase and the mechanisms through which TAOK1 mutations lead to neuropathology are unknown. Here, we showed that TAOK1 is highly expressed in neurons within the brain, and has a functional role in remodeling the plasma membrane through direct association with phosphoinositides. We characterized four NDD-associated TAOK1 mutations, and demonstrated that these mutations render TAOK1 catalytically dead. Kinase dead TAOK1 mutants were aberrantly trapped in membrane-bound state, which induced exuberant membrane protrusions. Expression of TAOK1 disease mutants in hippocampal neurons led to abnormal growth of the dendritic arbor. The coiled-coil region C-terminal to the kinase domain are predicted to fold into a triple helix. We showed that this triple helix directly bound phospholipids, and was required for both TAOK1 membrane association and induction of aberrant protrusions. Further, TAOK1 mutants were rescued from their membrane-trapped state by exogenous expression of the isolated kinase domain. Utilizing mass-spectrometry, we identified critical residues in the triple helix phosphorylated by TAOK1 that autoregulated its plasma membrane association. These findings define a previously unknown function of TAOK1 as a unique plasma membrane remodeling kinase, and reveal the underlying mechanisms through which TAOK1 dysfunction leads to neurodevelopmental disorders.
- Citations
- 20
- FWCI
- 3.48
- Field percentile
- top 6%
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Tsc1 Deletion in Purkinje Neurons Disrupts the Axon Initial Segment, Impairing Excitability and Cerebellar Function
Samuel P. Brown, Achintya K. Jena, … Joseph L. Ransdell·Neurobiology of DiseasePeer-reviewed·Feb 25, 2025
- A complex of MAST1 and 14-3-3 regulates Tau phosphorylation in the developing cortex
Sumire Antonioli, Patrick Heisterkamp, … Thomas A. Leonard·Proceedings of the National Academy of SciencesPeer-reviewed·Sep 17, 2026
- ALS and FTD-associated missense mutations in TBK1 differentially disrupt mitophagy
O. Harding, C. S. Evans, … E. L. F. Holzbaur·bioRxiv·Apr 12, 2021
- Dystonia-associated TorsinA-ΔE mutation induces a gain-of-function interaction with XPO1 via its N-terminal hydrophobic segment
Haochen Cui, Yuntian Duan, … Baojin Ding·bioRxiv·Aug 21, 2026
- KIF1A-mediated trafficking is required for neuronal autophagy in human neurons
Carris Temera Borland, Jacob Popolow, Erika L.F. Holzbaur·bioRxiv·Jul 24, 2026
- The fine-tuning of synapse development by oxidative stress and autophagy requires presynaptic ATM kinase
Matthew J. Taylor, Syed Azan Ahmed, … Richard I. Tuxworth·bioRxiv·Apr 25, 2024