Engram-specific transcriptome profiling of contextual memory consolidation.
Priyanka Rao-RuizJonathan J CoueyIvo M MarceloChristian G BouwkampDenise E SlumpMariana R MatosRolinka J van der LooGabriela J MartinsMirjam C G N van den HoutWilfred F J Van IJckenRui M CostaMichel C van den OeverSteven A KushnerPublished in: Nature communications (2019)
Sparse populations of neurons in the dentate gyrus (DG) of the hippocampus are causally implicated in the encoding of contextual fear memories. However, engram-specific molecular mechanisms underlying memory consolidation remain largely unknown. Here we perform unbiased RNA sequencing of DG engram neurons 24 h after contextual fear conditioning to identify transcriptome changes specific to memory consolidation. DG engram neurons exhibit a highly distinct pattern of gene expression, in which CREB-dependent transcription features prominently (P = 6.2 × 10-13), including Atf3 (P = 2.4 × 10-41), Penk (P = 1.3 × 10-15), and Kcnq3 (P = 3.1 × 10-12). Moreover, we validate the functional relevance of the RNAseq findings by establishing the causal requirement of intact CREB function specifically within the DG engram during memory consolidation, and identify a novel group of CREB target genes involved in the encoding of long-term memory.