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      A zebrafish genetic screen identifies neuromedin U as a regulator of sleep/wake states

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          Summary

          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 corticotrophin-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 likely 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.

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          Author and article information

          Journal
          8809320
          1600
          Neuron
          Neuron
          Neuron
          0896-6273
          1097-4199
          12 January 2016
          17 February 2016
          17 February 2017
          : 89
          : 4
          : 842-856
          Affiliations
          [1 ]Division of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA, 91125, USA
          [2 ]Department of Cell and Developmental Biology, University College London, London, WC1E 6BT, UK
          [3 ]Departments of Molecular and Cellular Biology, and Stem Cell and Regenerative Biology, Harvard University, Cambridge, MA, 02138, USA
          [4 ]Center for Cancer Systems Biology and Department of Cancer Biology, Dana-Farber Cancer Institute, and Department of Genetics, Harvard Medical School, Boston, MA 02115, USA
          [5 ]Center for Brain Science, Harvard University, Cambridge, MA, 02138, USA
          [6 ]Division of Sleep Medicine, Harvard University, Cambridge, MA, 02138, USA
          Author notes
          [*]

          co-first authors,

          [$]

          co-second authors.

          [†]

          Department of Neurobiology, Northwestern University, Evanston, IL, 60208

          [‡]

          Program in Biological Sciences, Northwestern University, Evanston, IL, 60208

          [§]

          Division of Science and Math, and Center for Genomics and Systems Biology (CGSB), New York University Abu Dhabi, Abu Dhabi, United Arab Emirates.

          Article
          PMC4851465 PMC4851465 4851465 nihpa750662
          10.1016/j.neuron.2016.01.007
          4851465
          26889812
          b750203b-57cd-4f6a-a701-d8afeb641408
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