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组蛋白赖氨酸甲基化:记忆和行为的关键调节因子。

Histone lysine methylation: critical regulator of memory and behavior.

出版信息

Rev Neurosci. 2013;24(4):375-87. doi: 10.1515/revneuro-2013-0008.

Abstract

Histone lysine methylation is a well-established transcriptional mechanism for the regulation of gene expression changes in eukaryotic cells and is now believed to function in neurons of the central nervous system to mediate the process of memory formation and behavior. In mature neurons, methylation of histone proteins can serve to both activate and repress gene transcription. This is in stark contrast to other epigenetic modifications, including histone acetylation and DNA methylation, which have largely been associated with one transcriptional state in the brain. In this review, we discuss the evidence for histone methylation mechanisms in the coordination of complex cognitive processes such as long-term memory formation and storage. In addition, we address the current literature highlighting the role of histone methylation in intellectual disability, addiction, schizophrenia, autism, depression, and neurodegeneration. Further, we discuss histone methylation within the context of other epigenetic modifications and the potential advantages of exploring this newly identified mechanism of cognition, emphasizing the possibility that this molecular process may provide an alternative locus for intervention in long-term psychopathologies that cannot be clearly linked to genes or environment alone.

摘要

组蛋白赖氨酸甲基化是真核细胞中基因表达变化调控的一种成熟的转录机制,现在被认为在中枢神经系统的神经元中发挥作用,介导记忆形成和行为的过程。在成熟的神经元中,组蛋白的甲基化既可以激活也可以抑制基因转录。这与其他表观遗传修饰形成鲜明对比,包括组蛋白乙酰化和 DNA 甲基化,它们在很大程度上与大脑中的一种转录状态相关。在这篇综述中,我们讨论了组蛋白甲基化机制在协调复杂认知过程(如长期记忆形成和存储)中的证据。此外,我们还讨论了当前的文献强调了组蛋白甲基化在智力障碍、成瘾、精神分裂症、自闭症、抑郁和神经退行性变中的作用。此外,我们还在其他表观遗传修饰的背景下讨论了组蛋白甲基化,并强调了探索这一新发现的认知机制的可能性,指出该分子过程可能为长期精神病理学提供一个替代的干预靶点,这些精神病理学不能仅归因于基因或环境。

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