Experimentally induced active and quiet sleep engage non-overlapping transcriptomes in Drosophila

Author:

Anthoney Niki1,Tainton-Heap Lucy A.L.1,Luong Hang2,Notaras Eleni1,Zhao Qiongyi1,Perry Trent2ORCID,Batterham Philip2,Shaw Paul J.3,van Swinderen Bruno1ORCID

Affiliation:

1. Queensland Brain Institute, The University of Queensland, Brisbane, QLD 4072 Australia

2. School of BioSciences, The University of Melbourne, Melbourne, VIC 3052 Australia

3. Department of Neuroscience, Washington University School of Medicine, St. Louis, MO USA

Abstract

Sleep in mammals is broadly classified into two different categories: rapid eye movement (REM) sleep and slow wave sleep (SWS), and accordingly REM and SWS are thought to achieve a different set of functions. The fruit fly Drosophila melanogaster is increasingly being used as a model to understand sleep functions, although it remains unclear if the fly brain also engages in different kinds of sleep as well. Here, we compare two commonly used approaches for studying sleep experimentally in Drosophila: optogenetic activation of sleep-promoting neurons and provision of a sleep-promoting drug, Gaboxadol. We find that these different sleep-induction methods have similar effects on increasing sleep duration, but divergent effects on brain activity. Transcriptomic analysis reveals that drug-induced deep sleep (‘quiet’ sleep) mostly downregulates metabolism genes, whereas optogenetic ‘active’ sleep upregulates a wide range of genes relevant to normal waking functions. This suggests that optogenetics and pharmacological induction of sleep in Drosophila promote different features of sleep, which engage different sets of genes to achieve their respective functions.

Publisher

eLife Sciences Publications, Ltd

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