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The zebrafish mutant dreammist implicates sodium homeostasis in sleep regulation.


ABSTRACT: Sleep is a nearly universal feature of animal behaviour, yet many of the molecular, genetic, and neuronal substrates that orchestrate sleep/wake transitions lie undiscovered. Employing a viral insertion sleep screen in larval zebrafish, we identified a novel gene, dreammist (dmist), whose loss results in behavioural hyperactivity and reduced sleep at night. The neuronally expressed dmist gene is conserved across vertebrates and encodes a small single-pass transmembrane protein that is structurally similar to the Na+,K+-ATPase regulator, FXYD1/Phospholemman. Disruption of either fxyd1 or atp1a3a, a Na+,K+-ATPase alpha-3 subunit associated with several heritable movement disorders in humans, led to decreased night-time sleep. Since atpa1a3a and dmist mutants have elevated intracellular Na+ levels and non-additive effects on sleep amount at night, we propose that Dmist-dependent enhancement of Na+ pump function modulates neuronal excitability to maintain normal sleep behaviour.

SUBMITTER: Barlow IL 

PROVIDER: S-EPMC10406431 | biostudies-literature | 2023 Aug

REPOSITORIES: biostudies-literature

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The zebrafish mutant <i>dreammist</i> implicates sodium homeostasis in sleep regulation.

Barlow Ida L IL   Mackay Eirinn E   Wheater Emily E   Goel Aimee A   Lim Sumi S   Zimmerman Steve S   Woods Ian I   Prober David A DA   Rihel Jason J  

eLife 20230807


Sleep is a nearly universal feature of animal behaviour, yet many of the molecular, genetic, and neuronal substrates that orchestrate sleep/wake transitions lie undiscovered. Employing a viral insertion sleep screen in larval zebrafish, we identified a novel gene, <i>dreammist</i> (<i>dmist</i>), whose loss results in behavioural hyperactivity and reduced sleep at night. The neuronally expressed <i>dmist</i> gene is conserved across vertebrates and encodes a small single-pass transmembrane prote  ...[more]

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