# TAOK2 controls synaptic plasticity and anxiety via ERK and calcium signaling

**Authors:** Wenbo Ma, Inanna Warnhoff, Marius Stephan, Xiao Ma, Kerstin Dehne, Paul Volkmann, Nirmal Kannaiyan, Ben Brankatschk, Niels Jensen, Moritz J. Rossner, Volker Scheuss, Michael C. Wehr

PMC · DOI: 10.1016/j.isci.2025.113712 · iScience · 2025-10-09

## TL;DR

TAOK2 is important for brain cell communication and behavior, and its loss causes problems in signaling and anxiety-like behavior in mice.

## Contribution

This study reveals that TAOK2 regulates synaptic plasticity and anxiety via ERK and calcium signaling in excitatory neurons.

## Key findings

- TAOK2 loss disrupts ERK/MAPK and calcium signaling in cortical neurons.
- TAOK2-deficient neurons show reduced synaptic density and connectivity.
- TAOK2 knockout mice display anxiety-related behavior in open field tests.

## Abstract

The kinase thousand and one amino acid kinase 2 (TAOK2) regulates dendritic architecture and synaptic plasticity and is implicated in neurodevelopmental and neuropsychiatric disorders, including autism and schizophrenia. Here, we investigated TAOK2 function by creating an Emx1-Cre-driven, excitatory-neuron-specific conditional Taok2 knockout (Taok2 cKO) mouse line. Pathway profiling in Taok2 cKO primary cortical neurons revealed impaired extracellular regulated kinase (ERK)/mitogen-activated protein kinase (MAPK) and calcium signaling after AMPA, BDNF, or bicuculline stimulation. These results were validated by reduced p-ERK1/2 protein levels and decreased calcium flux. Cultured Taok2 cKO neurons displayed reduced synaptic density and connectivity. Single-nucleus RNA sequencing of medial prefrontal cortex identified dysregulated gene expression enriched for postsynaptic MAPK and calcium pathways within cortical layers 2/3 and 4/5. Taok2 cKO mice exhibited an anxiety-related thigmotactic behavior in the open field test. Our findings demonstrate that TAOK2 loss in excitatory cortical neurons disrupts synaptic signaling and connectivity, drives behavioral abnormalities, and positions TAOK2 as a potential drug target for neuropsychiatric disorders.

•TAOK2 loss in excitatory cortical neurons disrupts ERK/MAPK and calcium signaling•TAOK2-deficient neurons show reduced synaptic density and connectivity in culture•snRNA-seq reveals transcriptional changes in cortical postsynaptic signaling•Taok2 conditional knockout mice display anxiety-related behavior in open field test

TAOK2 loss in excitatory cortical neurons disrupts ERK/MAPK and calcium signaling

TAOK2-deficient neurons show reduced synaptic density and connectivity in culture

snRNA-seq reveals transcriptional changes in cortical postsynaptic signaling

Taok2 conditional knockout mice display anxiety-related behavior in open field test

Molecular neuroscience; Cellular neuroscience; Transcriptomics

## Linked entities

- **Genes:** TAOK2 (TAO kinase 2) [NCBI Gene 9344], EPHB2 (EPH receptor B2) [NCBI Gene 2048], MAPK (mitogen activated kinase-like protein) [NCBI Gene 7446652]
- **Proteins:** PERK12 (Protein kinase superfamily protein)
- **Chemicals:** AMPA (PubChem CID 1221), bicuculline (PubChem CID 2376)
- **Diseases:** autism (MONDO:0005260), schizophrenia (MONDO:0005090)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** Taok2 (TAO kinase 2) [NCBI Gene 381921] {aka 1110033K02Rik, B230344N16, MAP3K17, PSK, PSK1, TAO1}, Bdnf (brain derived neurotrophic factor) [NCBI Gene 12064], Mapk1 (mitogen-activated protein kinase 1) [NCBI Gene 26413] {aka 9030612K14Rik, ERK, Erk2, MAPK2, PRKM2, Prkm1}, Emx1 (empty spiracles homeobox 1) [NCBI Gene 13796]
- **Diseases:** behavioral abnormalities (MESH:D001523), anxiety (MESH:D001007), autism (MESH:D001321), schizophrenia (MESH:D012559)
- **Chemicals:** calcium (MESH:D002118), bicuculline (MESH:D001640), AMPA (MESH:D018350)
- **Species:** Mus musculus (house mouse, species) [taxon 10090]

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12590003/full.md

## References

74 references — full list in the complete paper: https://tomesphere.com/paper/PMC12590003/full.md

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Source: https://tomesphere.com/paper/PMC12590003