Mapping the spatial transcriptomic signature of the hippocampus during memory consolidation.
Yann VanrobaeysUtsav MukherjeeLucy LangmackStacy E BeyerEthan BahlLi-Chun LinJacob J MichaelsonTed AbelSnehajyoti ChatterjeePublished in: Nature communications (2023)
Memory consolidation involves discrete patterns of transcriptional events in the hippocampus. Despite the emergence of single-cell transcriptomic profiling techniques, mapping the transcriptomic signature across subregions of the hippocampus has remained challenging. Here, we utilized unbiased spatial sequencing to delineate transcriptome-wide gene expression changes across subregions of the dorsal hippocampus of male mice following learning. We find that each subregion of the hippocampus exhibits distinct yet overlapping transcriptomic signatures. The CA1 region exhibited increased expression of genes related to transcriptional regulation, while the DG showed upregulation of genes associated with protein folding. Importantly, our approach enabled us to define the transcriptomic signature of learning within two less-defined hippocampal subregions, CA1 stratum radiatum, and oriens. We demonstrated that CA1 subregion-specific expression of a transcription factor subfamily has a critical functional role in the consolidation of long-term memory. This work demonstrates the power of spatial molecular approaches to reveal simultaneous transcriptional events across the hippocampus during memory consolidation.
Keyphrases
- single cell
- rna seq
- gene expression
- cerebral ischemia
- transcription factor
- prefrontal cortex
- poor prognosis
- high throughput
- working memory
- cognitive impairment
- genome wide
- dna methylation
- high resolution
- binding protein
- cell proliferation
- subarachnoid hemorrhage
- spinal cord
- spinal cord injury
- long non coding rna
- single molecule
- blood brain barrier
- molecular dynamics simulations
- dna binding
- heat stress
- amino acid