TY - JOUR
T1 - A Zebrafish Genetic Screen Identifies Neuromedin U as a Regulator of Sleep/Wake States
AU - Chiu, Cindy N.
AU - Rihel, Jason
AU - Lee, Daniel A.
AU - Singh, Chanpreet
AU - Mosser, Eric A.
AU - Chen, Shijia
AU - Sapin, Viveca
AU - Pham, Uyen
AU - Engle, Jae
AU - Niles, Brett J.
AU - Montz, Christin J.
AU - Chakravarthy, Sridhara
AU - Zimmerman, Steven
AU - Salehi-Ashtiani, Kourosh
AU - Vidal, Marc
AU - Schier, Alexander F.
AU - Prober, David A.
N1 - Publisher Copyright:
© 2016 Elsevier Inc.
PY - 2016/2/17
Y1 - 2016/2/17
N2 - Neuromodulation of arousal states ensures that an animal appropriately responds to its environment and engages in behaviors necessary for survival. However, the molecular and circuit properties underlying neuromodulation of arousal states such as sleep and wakefulness remain unclear. To tackle this challenge in a systematic and unbiased manner, we performed a genetic overexpression screen to identify genes that affect larval zebrafish arousal. We found that the neuropeptide neuromedin U (Nmu) promotes hyperactivity and inhibits sleep in zebrafish larvae, whereas nmu mutant animals are hypoactive. We show that Nmu-induced arousal requires Nmu receptor 2 and signaling via corticotropin releasing hormone (Crh) receptor 1. In contrast to previously proposed models, we find that Nmu does not promote arousal via the hypothalamic-pituitary-adrenal axis, but rather probably acts via brainstem crh-expressing neurons. These results reveal an unexpected functional and anatomical interface between the Nmu system and brainstem arousal systems that represents a novel wake-promoting pathway. Video Abstract: Chiu et al. perform a genetic screen in zebrafish and identify Nmu as a regulator of sleep/wake behaviors. They show that Nmu overexpression activates brainstem Crh neurons and that Nmu-induced arousal requires Crh signaling, thus identifying a novel vertebrate arousal circuit.
AB - Neuromodulation of arousal states ensures that an animal appropriately responds to its environment and engages in behaviors necessary for survival. However, the molecular and circuit properties underlying neuromodulation of arousal states such as sleep and wakefulness remain unclear. To tackle this challenge in a systematic and unbiased manner, we performed a genetic overexpression screen to identify genes that affect larval zebrafish arousal. We found that the neuropeptide neuromedin U (Nmu) promotes hyperactivity and inhibits sleep in zebrafish larvae, whereas nmu mutant animals are hypoactive. We show that Nmu-induced arousal requires Nmu receptor 2 and signaling via corticotropin releasing hormone (Crh) receptor 1. In contrast to previously proposed models, we find that Nmu does not promote arousal via the hypothalamic-pituitary-adrenal axis, but rather probably acts via brainstem crh-expressing neurons. These results reveal an unexpected functional and anatomical interface between the Nmu system and brainstem arousal systems that represents a novel wake-promoting pathway. Video Abstract: Chiu et al. perform a genetic screen in zebrafish and identify Nmu as a regulator of sleep/wake behaviors. They show that Nmu overexpression activates brainstem Crh neurons and that Nmu-induced arousal requires Crh signaling, thus identifying a novel vertebrate arousal circuit.
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U2 - 10.1016/j.neuron.2016.01.007
DO - 10.1016/j.neuron.2016.01.007
M3 - Article
C2 - 26889812
AN - SCOPUS:84958212456
SN - 0896-6273
VL - 89
SP - 842
EP - 856
JO - Neuron
JF - Neuron
IS - 4
ER -