| Literature DB >> 34782479 |
Jessica E Schwarz1,2, Anna N King1,2, Cynthia T Hsu1,2, Annika F Barber1,2, Amita Sehgal3,2.
Abstract
Sleep is controlled by homeostatic mechanisms, which drive sleep after wakefulness, and a circadian clock, which confers the 24-h rhythm of sleep. These processes interact with each other to control the timing of sleep in a daily cycle as well as following sleep deprivation. However, the mechanisms by which they interact are poorly understood. We show here that hugin + neurons, previously identified as neurons that function downstream of the clock to regulate rhythms of locomotor activity, are also targets of the sleep homeostat. Sleep deprivation decreases activity of hugin + neurons, likely to suppress circadian-driven activity during recovery sleep, and ablation of hugin + neurons promotes sleep increases generated by activation of the homeostatic sleep locus, the dorsal fan-shaped body (dFB). Also, mutations in peptides produced by the hugin + locus increase recovery sleep following deprivation. Transsynaptic mapping reveals that hugin + neurons feed back onto central clock neurons, which also show decreased activity upon sleep loss, in a Hugin peptide-dependent fashion. We propose that hugin + neurons integrate circadian and sleep signals to modulate circadian circuitry and regulate the timing of sleep.Entities:
Keywords: Drosophila; circadian rhythms; circuit; neuropeptides; sleep homeostasis
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Year: 2021 PMID: 34782479 PMCID: PMC8617458 DOI: 10.1073/pnas.2111183118
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 11.205