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

机译:BET蛋白Brd4激活神经元的转录,BET抑制剂Jq1阻断小鼠的记忆

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摘要

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.
机译:转录的精确调控对于记忆形成的细胞机制至关重要。然而,神经元刺激与直接与组蛋白修饰相互作用以激活神经元转录的蛋白质之间的联系仍不清楚。 Brd4是溴结构域和末端外域(BET)蛋白家族的成员,该家族与乙酰化组蛋白结合,并且是许多细胞类型(包括响应外部提示的转录)中转录的关键调控因子。小分子BET抑制剂正在临床试验中,但是关于Brd4在大脑中的功能几乎一无所知。在这里,我们显示Brd4介导了学习和记忆的转录调控。 Brd4功能的丧失会影响关键的突触蛋白,从而导致小鼠记忆力减退,但也会降低癫痫发作的敏感性。因此,Brd4提供了神经元激活与记忆形​​成过程中发生的转录反应之间的关键联系。

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