Nutrigenomic regulation of sensory plasticity.
Ha Yeon SungAnoumid VaziriDaniel WilinskiRiley K R WoernerPeter L FreddolinoMonica DusPublished in: eLife (2023)
Diet profoundly influences brain physiology, but how metabolic information is transmuted into neural activity and behavior changes remains elusive. Here, we show that the metabolic enzyme O-GlcNAc Transferase (OGT) moonlights on the chromatin of the D. melanogaster gustatory neurons to instruct changes in chromatin accessibility and transcription that underlie sensory adaptations to a high-sugar diet. OGT works synergistically with the Mitogen Activated Kinase/Extracellular signal Regulated Kinase (MAPK/ERK) rolled and its effector stripe (also known as EGR2 or Krox20) to integrate activity information. OGT also cooperates with the epigenetic silencer Polycomb Repressive Complex 2.1 (PRC2.1) to decrease chromatin accessibility and repress transcription in the high-sugar diet. This integration of nutritional and activity information changes the taste neurons' responses to sugar and the flies' ability to sense sweetness. Our findings reveal how nutrigenomic signaling generates neural activity and behavior in response to dietary changes in the sensory neurons.
Keyphrases
- transcription factor
- gene expression
- genome wide
- dna damage
- spinal cord
- physical activity
- signaling pathway
- weight loss
- protein kinase
- dna methylation
- healthcare
- health information
- pi k akt
- multiple sclerosis
- white matter
- regulatory t cells
- immune response
- brain injury
- single cell
- blood brain barrier
- high intensity
- subarachnoid hemorrhage
- nuclear factor
- type iii
- cerebral ischemia