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Nat Neurosci. 2015 Oct;18(10):1464-73. doi: 10.1038/nn.4095. Epub 2015 Aug 24.

BET protein Brd4 activates transcription in neurons and BET inhibitor Jq1 blocks memory in mice.

Author information

1
Laboratory of Chromatin Biology and Epigenetics, The Rockefeller University, New York, New York, USA.
2
Laboratory of Molecular Neuro-oncology, The Rockefeller University, New York, New York, USA.

Abstract

Precise regulation of transcription is crucial for the cellular mechanisms underlying memory formation. However, the link between neuronal stimulation and the proteins that directly interact with histone modifications to activate transcription in neurons remains unclear. Brd4 is a member of the bromodomain and extra-terminal domain (BET) protein family, which binds acetylated histones and is a critical regulator of transcription in many cell types, including transcription in response to external cues. Small molecule BET inhibitors are in clinical trials, yet almost nothing is known about Brd4 function in the brain. Here we show that Brd4 mediates the transcriptional regulation underlying learning and memory. The loss of Brd4 function affects critical synaptic proteins, which results in memory deficits in mice but also decreases seizure susceptibility. Thus Brd4 provides a critical link between neuronal activation and the transcriptional responses that occur during memory formation.

PMID:
26301327
PMCID:
PMC4752120
DOI:
10.1038/nn.4095
[Indexed for MEDLINE]
Free PMC Article

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