Kupke Janina, Loizou Stefanos, Bengtson C Peter, Sticht Carsten, Oliveira Ana M M
Department of Neurobiology, Interdisciplinary Center for Neurosciences, Heidelberg University, Heidelberg, Germany.
Department of Neurobiology, Interdisciplinary Center for Neurosciences, Heidelberg University, Heidelberg, Germany; Department of Molecular and Cellular Cognition Research, Central Institute of Mental Health, Medical Faculty Mannheim, Heidelberg University, Mannheim, Germany.
Biol Psychiatry. 2025 Sep 1;98(5):394-403. doi: 10.1016/j.biopsych.2025.01.016. Epub 2025 Jan 27.
Long-term fear memory storage involves gradual reorganization of supporting brain regions over time, a process termed systems consolidation. Memories initially rely on the hippocampus but gradually shift dependence to the neocortex. Although hippocampal activity drives this transfer, the molecular basis of systems consolidation is largely unknown. DNA methylation changes accompany persistent fear memory formation in the hippocampus and cortex, but its causal role in memory storage and systems consolidation remains unclear.
We investigated the role of hippocampal DNA methylation in fear memory persistence through multiple approaches. Using recombinant adeno-associated virus (rAAV)-mediated gene transfer, we overexpressed or knocked down a DNA methyltransferase (DNMT3A2) in the dorsal hippocampus of mice and assessed its impact on fear memory duration. Engram tagging and manipulation tools were applied to study cortical fear engram stabilization. Finally, RNA sequencing analysis was used to identify transcriptional changes driven by DNMT3A2 overexpression.
Overexpression of hippocampal DNMT3A2 induced a persistent fear memory, while its knockdown impaired remote memory recall. RNA sequencing revealed that DNMT3A2 overexpression modified the expression of synaptic transmission regulatory genes. Furthermore, genetic engram tagging and manipulation revealed that hippocampal DNA methylation promoted the transfer of the fear memory trace from the hippocampus to the cortex and the stabilization of cortical fear memory traces.
Our findings demonstrate that hippocampal DNA methylation regulates the long-term storage of persistent fear memories by facilitating the transfer of memory traces from the hippocampus to the cortex and cortical stabilization. These results highlight DNA methylation as a key molecular mechanism underlying systems consolidation and long-term fear memory storage.
长期恐惧记忆的存储涉及支持性脑区随时间的逐渐重组,这一过程称为系统巩固。记忆最初依赖海马体,但逐渐将依赖性转移至新皮层。尽管海马体活动驱动这种转移,但系统巩固的分子基础在很大程度上尚不清楚。DNA甲基化变化伴随海马体和皮层中持续性恐惧记忆的形成,但其在记忆存储和系统巩固中的因果作用仍不清楚。
我们通过多种方法研究了海马体DNA甲基化在恐惧记忆持续性中的作用。利用重组腺相关病毒(rAAV)介导的基因转移,我们在小鼠背侧海马体中过表达或敲低一种DNA甲基转移酶(DNMT3A2),并评估其对恐惧记忆持续时间的影响。应用记忆印记标记和操纵工具来研究皮层恐惧记忆印记的稳定化。最后,使用RNA测序分析来鉴定由DNMT3A2过表达驱动的转录变化。
海马体DNMT3A2的过表达诱导了持续性恐惧记忆,而其敲低则损害了远期记忆的回忆。RNA测序显示,DNMT3A2过表达改变了突触传递调节基因的表达。此外,基因记忆印记标记和操纵表明,海马体DNA甲基化促进了恐惧记忆痕迹从海马体向皮层的转移以及皮层恐惧记忆痕迹的稳定化。
我们的研究结果表明,海马体DNA甲基化通过促进记忆痕迹从海马体向皮层的转移以及皮层稳定化来调节持续性恐惧记忆的长期存储。这些结果突出了DNA甲基化作为系统巩固和长期恐惧记忆存储潜在的关键分子机制。