Abstract
Sleep is important for memory consolidation and is responsive to waking experience. Clock circuitry is uniquely positioned to coordinate interactions between processes underlying memory and sleep need. Flies increase sleep both after exposure to an enriched social environment and after protocols that induce long-term memory. We found that flies mutant for rutabaga, period, and blistered were deficient for experience-dependent increases in sleep. Rescue of each of these genes within the ventral lateral neurons (LNVs) restores increased sleep after social enrichment. Social experiences that induce increased sleep were associated with an increase in the number of synaptic terminals in the LNV projections into the medulla. The number of synaptic terminals was reduced during sleep and this decline was prevented by sleep deprivation.
MeSH Terms
Adenylyl Cyclases/genetics,physiology
Animals
Biological Clocks/genetics
Brain/physiology
Circadian Rhythm/genetics
Drosophila Proteins/genetics,metabolism,physiology
Drosophila melanogaster/cytology,genetics,physiology
ErbB Receptors/genetics,metabolism
Female
Genes, Insect
Male
Memory
Models, Animal
Mutation
Neuronal Plasticity
Neurons/physiology,ultrastructure
Nuclear Proteins/genetics,physiology
Period Circadian Proteins
Presynaptic Terminals/physiology,ultrastructure
Receptors, Invertebrate Peptide/genetics,metabolism
Serum Response Factor/genetics,physiology
Sleep/physiology
Sleep Deprivation
Social Behavior
Synapses/physiology
Chemicals
Drosophila Proteins
Nuclear Proteins
PER protein, Drosophila
Period Circadian Proteins
Receptors, Invertebrate Peptide
Serum Response Factor
bs protein, Drosophila
Egfr protein, Drosophila
ErbB Receptors
Adenylyl Cyclases
Rut protein, Drosophila
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Donlea Jeffrey M
Department of Anatomy and Neurobiology, Washington University in St. Louis, 660 South Euclid Avenue, St. Louis, Missouri, USA.
Ramanan Narendrakumar
Shaw Paul J
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