Literature DB >> 28951451

The Intellectual Disability and Schizophrenia Associated Transcription Factor TCF4 Is Regulated by Neuronal Activity and Protein Kinase A.

Mari Sepp1, Hanna Vihma2, Kaja Nurm2, Mari Urb2, Stephanie Cerceo Page3, Kaisa Roots2, Anu Hark2, Brady J Maher3,4,5, Priit Pruunsild2, Tõnis Timmusk1.   

Abstract

Transcription factor 4 (TCF4 also known as ITF2 or E2-2) is a basic helix-loop-helix (bHLH) protein associated with Pitt-Hopkins syndrome, intellectual disability, and schizophrenia (SCZ). Here, we show that TCF4-dependent transcription in cortical neurons cultured from embryonic rats of both sexes is induced by neuronal activity via soluble adenylyl cyclase and protein kinase A (PKA) signaling. PKA phosphorylates TCF4 directly and a PKA phosphorylation site in TCF4 is necessary for its transcriptional activity in cultured neurons and in the developing brain in vivo We also demonstrate that Gadd45g (growth arrest and DNA damage inducible gamma) is a direct target of neuronal-activity-induced, TCF4-dependent transcriptional regulation and that TCF4 missense variations identified in SCZ patients alter the transcriptional activity of TCF4 in neurons. This study identifies a new role for TCF4 as a neuronal-activity-regulated transcription factor, offering a novel perspective on the association of TCF4 with cognitive disorders.SIGNIFICANCE STATEMENT The importance of the basic helix-loop-helix transcription factor transcription factor 4 (TCF4) in the nervous system is underlined by its association with common and rare cognitive disorders. In the current study, we show that TCF4-controlled transcription in primary cortical neurons is induced by neuronal activity and protein kinase A. Our results support the hypotheses that dysregulation of neuronal-activity-dependent signaling plays a significant part in the etiology of neuropsychiatric and neurodevelopmental disorders.
Copyright © 2017 the authors 0270-6474/17/3710516-12$15.00/0.

Entities:  

Keywords:  E2-2; ITF2; Pitt–Hopkins syndrome; bHLH; neuronal activity; schizophrenia

Mesh:

Substances:

Year:  2017        PMID: 28951451      PMCID: PMC5656997          DOI: 10.1523/JNEUROSCI.1151-17.2017

Source DB:  PubMed          Journal:  J Neurosci        ISSN: 0270-6474            Impact factor:   6.167


  73 in total

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6.  Partial deletion of TCF4 in three generation family with non-syndromic intellectual disability, without features of Pitt-Hopkins syndrome.

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1.  Transcription Factor 4 loss-of-function is associated with deficits in progenitor proliferation and cortical neuron content.

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Review 2.  Modulation of Neocortical Development by Early Neuronal Activity: Physiology and Pathophysiology.

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3.  Analysis of the expression pattern of the schizophrenia-risk and intellectual disability gene TCF4 in the developing and adult brain suggests a role in development and plasticity of cortical and hippocampal neurons.

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Journal:  Mol Autism       Date:  2018-03-22       Impact factor: 7.509

4.  The Psychiatric Risk Gene Transcription Factor 4 (TCF4) Regulates Neurodevelopmental Pathways Associated With Schizophrenia, Autism, and Intellectual Disability.

Authors:  Marc P Forrest; Matthew J Hill; David H Kavanagh; Katherine E Tansey; Adrian J Waite; Derek J Blake
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5.  Daughterless, the Drosophila orthologue of TCF4, is required for associative learning and maintenance of the synaptic proteome.

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Review 7.  Transcription factor 4 and its association with psychiatric disorders.

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Journal:  Transl Psychiatry       Date:  2021-01-05       Impact factor: 6.222

8.  Enriched environment ameliorates adult hippocampal neurogenesis deficits in Tcf4 haploinsufficient mice.

Authors:  Katharina Braun; Benjamin M Häberle; Marie-Theres Wittmann; D Chichung Lie
Journal:  BMC Neurosci       Date:  2020-11-23       Impact factor: 3.288

Review 9.  Molecular and Cellular Function of Transcription Factor 4 in Pitt-Hopkins Syndrome.

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Review 10.  Functional Significance of the Adcy10-Dependent Intracellular cAMP Compartments.

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