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    <responseDate>2026-10-14T18:55:45Z</responseDate>
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            <header>
                <identifier>oai:data.mendeley.com/k2n7jwx9rn.1</identifier>
                <datestamp>2025-10-02T14:20:14Z</datestamp>
            </header>
            <metadata><oai_dc:dc xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
    <dc:creator id="https://orcid.org/0000-0003-1770-8323">Wehr, Michael</dc:creator>
    <dc:title>TAOK2 controls synaptic plasticity and anxiety through ERK and calcium signaling</dc:title>
    <dc:publisher>Mendeley Data</dc:publisher>
    <dc:description>The kinase 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 ERK/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, driving behavioral
abnormalities, and position TAOK2 as a potential drug target for neuropsychiatric disorders.</dc:description>
    <dc:subject>Animal Behavior</dc:subject>
    <dc:subject>Next Generation Sequencing</dc:subject>
    <dc:subject>Single-Cell RNA Sequencing</dc:subject>
    <dc:contributor>Ma, Wenbo</dc:contributor>
    <dc:contributor>Warnhoff, Inanna</dc:contributor>
    <dc:contributor>Stephan, Marius</dc:contributor>
    <dc:contributor>Ma, Xiao</dc:contributor>
    <dc:contributor>Dehne, Kerstin</dc:contributor>
    <dc:contributor>Volkmann, Paul</dc:contributor>
    <dc:contributor id="https://orcid.org/0000-0002-7408-6842">Kannaiyan, Nirmal</dc:contributor>
    <dc:contributor>Brankatschk, Ben</dc:contributor>
    <dc:contributor id="https://orcid.org/0000-0001-8171-3333">Jensen, Niels</dc:contributor>
    <dc:contributor id="https://orcid.org/0000-0002-0667-3420">Rossner, Moritz J</dc:contributor>
    <dc:contributor>Scheuss, Volker</dc:contributor>
    <dc:type>Dataset</dc:type>
    <dc:identifier>doi:10.17632/k2n7jwx9rn.1</dc:identifier>
    <dc:identifier>oai:data.mendeley.com/k2n7jwx9rn.1</dc:identifier>
    <dc:rights>Creative Commons Attribution 4.0 International</dc:rights>
    <dc:rights>http://creativecommons.org/licenses/by/4.0</dc:rights>
    <dc:relation>https://data.mendeley.com/datasets/k2n7jwx9rn</dc:relation>
    <dc:date>2025-10-02T14:20:14Z</dc:date>
</oai_dc:dc></metadata>
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