Hakubi Center, Kyoto University Graduate School of Medicine, Konoecho, Yoshida, Sakyo-ku, Kyoto, Kyoto, 606-8315, Japan.
Laboratory for Phyloinformatics, RIKEN Center for Biosystems Dynamics Research, Kobe, 650-0047, Japan.
Nat Commun. 2021 Jan 27;12(1):628. doi: 10.1038/s41467-021-20898-x.
Consolidated memory can be preserved or updated depending on the environmental change. Although such conflicting regulation may happen during memory updating, the flexibility of memory updating may have already been determined in the initial memory consolidation process. Here, we explored the gating mechanism for activity-dependent transcription in memory consolidation, which is unexpectedly linked to the later memory updating in Drosophila. Through proteomic analysis, we discovered that the compositional change in the transcriptional repressor, which contains the histone deacetylase Rpd3 and CoRest, acts as the gating mechanism that opens and closes the time window for activity-dependent transcription. Opening the gate through the compositional change in Rpd3/CoRest is required for memory consolidation, but closing the gate through Rpd3/CoRest is significant to limit future memory updating. Our data indicate that the flexibility of memory updating is determined through the initial activity-dependent transcription, providing a mechanism involved in defining memory state.
根据环境变化,整合后的记忆可以被保存或更新。虽然在记忆更新过程中可能会发生这种相互冲突的调节,但记忆更新的灵活性可能已经在初始的记忆巩固过程中确定了。在这里,我们探讨了记忆巩固过程中活性依赖性转录的门控机制,出乎意料的是,它与果蝇后来的记忆更新有关。通过蛋白质组学分析,我们发现转录抑制因子的组成变化,其中包含组蛋白去乙酰化酶 Rpd3 和 CoRest,作为门控机制,开启和关闭活性依赖性转录的时间窗口。通过 Rpd3/CoRest 的组成变化打开门是记忆巩固所必需的,但通过 Rpd3/CoRest 关闭门对于限制未来的记忆更新是至关重要的。我们的数据表明,记忆更新的灵活性是通过初始的活性依赖性转录来决定的,为定义记忆状态提供了一种机制。