Genome-wide translational profiling of amygdala Crh-expressing neurons reveals role for CREB in fear extinction learning.
Kenneth M McCulloughChris ChatzinakosJakob HartmannGalen MissigRachael L NeveRobert J FensterWilliam A CarlezonNikolaos P DaskalakisKerry James ResslerPublished in: Nature communications (2020)
Fear and extinction learning are adaptive processes caused by molecular changes in specific neural circuits. Neurons expressing the corticotropin-releasing hormone gene (Crh) in central amygdala (CeA) are implicated in threat regulation, yet little is known of cell type-specific gene pathways mediating adaptive learning. We translationally profiled the transcriptome of CeA Crh-expressing cells (Crh neurons) after fear conditioning or extinction in mice using translating ribosome affinity purification (TRAP) and RNAseq. Differential gene expression and co-expression network analyses identified diverse networks activated or inhibited by fear vs extinction. Upstream regulator analysis demonstrated that extinction associates with reduced CREB expression, and viral vector-induced increased CREB expression in Crh neurons increased fear expression and inhibited extinction. These findings suggest that CREB, within CeA Crh neurons, may function as a molecular switch that regulates expression of fear and its extinction. Cell-type specific translational analyses may suggest targets useful for understanding and treating stress-related psychiatric illness.
Keyphrases
- poor prognosis
- genome wide
- gene expression
- prefrontal cortex
- spinal cord
- dna methylation
- binding protein
- long non coding rna
- sars cov
- single cell
- induced apoptosis
- mental health
- cell death
- transcription factor
- cell proliferation
- cell cycle arrest
- oxidative stress
- endoplasmic reticulum stress
- signaling pathway
- skeletal muscle
- rna seq
- genome wide identification
- capillary electrophoresis
- quality control