| Literature DB >> 28951451 |
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.Entities:
Keywords: E2-2; ITF2; Pitt–Hopkins syndrome; bHLH; neuronal activity; schizophrenia
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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