How sleep consolidates fear memories at the molecular level within individual engram neurons is unknown. Using activity-dependent tagging and sequencing, we profiled the DNA methylome and transcriptome of engram and non-engram nuclei from the basolateral amygdala (BLA) after contextual fear conditioning with and without post-learning sleep deprivation. Fear learning induces coordinated CpG and CpH DNA methylation remodeling specifically in engram neurons, with each showing unique temporal dynamics, revealing CpH methylation as a separate component of the engram's epigenetic signature. Interestingly, sleep deprivation partially reverses learning-induced methylation changes and impairs memory recall, indicating that sleep supports engram-specific epigenetic consolidation. Integrating the engram methylome with single-cell transcriptome profiling, we construct a multi-omic molecular atlas of the BLA fear engram and identify Mid1 as a learning- and sleep-regulated methylation target. BLA-wide and engram-specific Mid1 knockdown establishes its functional requirement for fear memory consolidation, providing an approach to identify behaviorally relevant epigenetic targets.
No takes yet. Share an insight, caveat, or question.
Chen et al. (2026) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: