4.7 Article

Drosophila DH31 Neuropeptide and PDF Receptor Regulate Night-Onset Temperature Preference

Journal

JOURNAL OF NEUROSCIENCE
Volume 36, Issue 46, Pages 11739-11754

Publisher

SOC NEUROSCIENCE
DOI: 10.1523/JNEUROSCI.0964-16.2016

Keywords

circadian rhythm; DH31; Drosophila; PDFR; temperature preference behavior; thermoregulation

Categories

Funding

  1. Cincinnati Children's Hospital
  2. Japan Science and Technology (JST)/Precursory Research for Embryonic Science and Technology (PRESTO)
  3. March of Dimes
  4. National Institutes of Health R01 Grant [GM107582]

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Body temperature exhibits rhythmic fluctuations over a 24 h period (Refinetti and Menaker, 1992) and decreases during the night, which is associated with sleep initiation (Gilbert et al., 2004; Krauchi, 2007 a, b). However, the underlying mechanism of this temperature decrease is largely unknown. We have previously shown that Drosophila exhibit a daily temperature preference rhythm (TPR), in which their preferred temperatures increase during the daytime and then decrease at the transition from day to night (night-onset) (Kaneko et al., 2012). Because Drosophila are small ectotherms, their body temperature is very close to that of the ambient temperature (Stevenson, 1985), suggesting that their TPR generates their body temperature rhythm. Here, we demonstrate that the neuropeptide diuretic horm one 31 (DH31) and pigment-dispersing factor receptor (PDFR) contribute to regulate the preferred temperature decrease at night-onset. We show that PDFR and tethered-DH31 expression in dorsal neurons 2 (DN2s) restore the preferred temperature decrease at night-onset, suggesting that DH31 acts on PDFR in DN2s. Notably, we previously showed that the molecular clock in DN2s is important for TPR. Although PDF (another ligand of PDFR) is a critical factor for locomotor activity rhythms, Pdf mutants exhibit normal preferred temperature decreases at night-onset. This suggests that DH31-PDFR signaling specifically regulates a preferred temperature decrease at night-onset. Thus, we propose that night-onset TPR and locomotor activity rhythms are differentially controlled not only by clock neurons but also by neuropeptide signaling in the brain.

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