Department of Biology, School of Arts and Sciences, University of Pennsylvania, Philadelphia, PA, USA.
Neuropsychopharmacology. 2013 Jan;38(1):62-76. doi: 10.1038/npp.2012.86. Epub 2012 Jun 6.
Long-term memory formation requires transcription and protein synthesis. Over the past few decades, a great amount of knowledge has been gained regarding the molecular players that regulate the transcriptional program linked to memory consolidation. Epigenetic mechanisms have been shown to be essential for the regulation of neuronal gene expression, and histone acetylation has been one of the most studied and best characterized. In this review, we summarize the lines of evidence that have shown the relevance of histone acetylation in memory in both physiological and pathological conditions. Great advances have been made in identifying the writers and erasers of histone acetylation marks during learning. However, the identities of the upstream regulators and downstream targets that mediate the effect of changes in histone acetylation during memory consolidation remain restricted to a handful of molecules. We outline a general model by which corepressors and coactivators regulate histone acetylation during memory storage and discuss how the recent advances in high-throughput sequencing have the potential to radically change our understanding of how epigenetic control operates in the brain.
长期记忆的形成需要转录和蛋白质合成。在过去的几十年中,人们已经获得了大量关于调节与记忆巩固相关的转录程序的分子参与者的知识。表观遗传机制对于神经元基因表达的调节至关重要,组蛋白乙酰化已成为研究最多和最具特征的机制之一。在这篇综述中,我们总结了组蛋白乙酰化在生理和病理条件下与记忆相关的证据。在识别学习过程中组蛋白乙酰化标记的写入器和擦除器方面已经取得了很大的进展。然而,介导记忆巩固过程中组蛋白乙酰化变化的上游调节剂和下游靶标仍然仅限于少数几种分子。我们概述了一个一般模型,其中核心抑制剂和共激活剂在记忆存储过程中调节组蛋白乙酰化,并讨论了高通量测序的最新进展如何有可能彻底改变我们对表观遗传控制在大脑中运作方式的理解。