Psychiatric Risk Gene Transcription Factor 4 Regulates Intrinsic Excitability of Prefrontal Neurons via Repression of SCN10a and KCNQ1

Matthew D D. Rannals, Gregory R R. Hamersky, Stephanie Cerceo C. Page, Morganne N N. Campbell, Aaron Briley, Ryan A A. Gallo, Ba Doi N Phan, Thomas M M. Hyde, Joel E E. Kleinman, Joo Heon H. Shin, Andrew E E. Jaffe, Daniel R R. Weinberger, Brady J J. Maher

Research output: Contribution to journalArticlepeer-review

Abstract

Transcription Factor 4 (TCF4) is a clinically pleiotropic gene associated with schizophrenia and Pitt-Hopkins syndrome (PTHS). To gain insight about the neurobiology of TCF4, we created an in vivo model of PTHS by suppressing Tcf4 expression in rat prefrontal neurons immediately prior to neurogenesis. This cell-autonomous genetic insult attenuated neuronal spiking by increasing the afterhyperpolarization. At the molecular level, using a novel technique called iTRAP that combined in utero electroporation and translating ribosome affinity purification, we identified increased translation of two ion channel genes, Kcnq1 and Scn10a. These ion channel candidates were validated by pharmacological rescue and molecular phenocopy. Remarkably, similar excitability deficits were observed in prefrontal neurons from a Tcf4+/tr mouse model of PTHS. Thus, we identify TCF4 as a regulator of neuronal intrinsic excitability in part by repression of Kcnq1 and Scn10a and suggest that this molecular function may underlie pathophysiology associated with neuropsychiatric disorders.

Original languageEnglish (US)
Pages (from-to)43-55
Number of pages13
JournalNeuron
Volume90
Issue number1
DOIs
StatePublished - Apr 6 2016

ASJC Scopus subject areas

  • Neuroscience(all)

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