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TNiK Is Required for Postsynaptic and Nuclear Signaling Pathways and Cognitive Function

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  • Marcelo P. Coba
  • Noboru H. Komiyama
  • Jess Nithianantharajah
  • Maksym V. Kopanitsa
  • Tim Indersmitten
  • Nathan G. Skene
  • Ellie J. Tuck
  • David G. Fricker
  • Kathryn A. Elsegood
  • Lianne E. Stanford
  • Nurudeen O. Afinowi
  • Lisa M. Saksida
  • Timothy J. Bussey
  • Thomas J. O'Dell
  • Seth G. N. Grant

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http://www.jneurosci.org/content/32/40/13987
Original languageEnglish
Pages (from-to)13987-13999
Number of pages13
JournalJournal of Neuroscience
Volume32
Issue number40
DOIs
Publication statusPublished - 3 Oct 2012

Abstract

Traf2 and NcK interacting kinase (TNiK) contains serine-threonine kinase and scaffold domains and has been implicated in cell proliferation and glutamate receptor regulation in vitro. Here we report its role in vivo using mice carrying a knock-out mutation. TNiK binds protein complexes in the synapse linking it to the NMDA receptor ( NMDAR) via AKAP9. NMDAR and metabotropic receptors bidirectionally regulate TNiK phosphorylation and TNiK is required for AMPA expression and synaptic function. TNiK also organizes nuclear complexes and in the absence of TNiK, there was a marked elevation in GSK3 beta and phosphorylation levels of its cognate phosphorylation sites on NeuroD1 with alterations in Wnt pathway signaling. We observed impairments in dentate gyrus neurogenesis in TNiK knock-out mice and cognitive testing using the touchscreen apparatus revealed impairments in pattern separation on a test of spatial discrimination. Object-location paired associate learning, which is dependent on glutamatergic signaling, was also impaired. Additionally, TNiK knock-out mice displayed hyperlocomotor behavior that could be rapidly reversed by GSK3 beta inhibitors, indicating the potential for pharmacological rescue of a behavioral phenotype. These data establish TNiK as a critical regulator of cognitive functions and suggest it may play a regulatory role in diseases impacting on its interacting proteins and complexes.

    Research areas

  • LONG-TERM POTENTIATION, AMPA RECEPTORS, MICE, PROGENITOR PROLIFERATION, DENTATE GYRUS, PROTEINS, SCHIZOPHRENIA, ADULT HIPPOCAMPAL NEUROGENESIS, SPATIAL-PATTERN SEPARATION, NEURONS

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