Abstract

Summary:Sleep remains a major mystery of biology, with little understood about its basic function. One of the most commonly proposed functions for sleep is the consolidation of memory1–3. However, as conditions like starvation require the organism to be awake and active4, the ability to switch to a memory consolidation mechanism that is not contingent on sleep may confer an evolutionary advantage. Here, we identify a novel adaptive circuit-based mechanism that enables Drosophila to form sleep-dependent and sleep-independent memory. Flies fed after appetitive conditioning needed increased sleep for memory consolidation, but flies starved after training did not require sleep to form memories. Memory in fed flies is mediated by the anterior-posterior α’/β’ neurons of the mushroom body (MB), while memory under starvation is mediated by medial α’/β’ neurons. Sleep-dependent and sleep-independent memory rely upon distinct dopaminergic neurons and corresponding MB output neurons. However, sleep and memory are coupled such that mushroom body neurons required for sleep-dependent memory also promote sleep. Flies lacking Neuropeptide F display sleep-dependent memory even when starved, suggesting that circuit selection is determined by hunger. This plasticity in memory circuits enables flies to retain essential information in changing environments.

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