4.8 Article

A nutrient-specific gut hormone arbitrates between courtship and feeding

Journal

NATURE
Volume 602, Issue 7898, Pages 632-+

Publisher

NATURE PORTFOLIO
DOI: 10.1038/s41586-022-04408-7

Keywords

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Funding

  1. NINDS [P30 NS047101]
  2. National Science Foundation [1429810]
  3. NIH [R01DK127516, R01DK092640, R01DC009597, K99DC016338]
  4. Div Of Biological Infrastructure
  5. Direct For Biological Sciences [1429810] Funding Source: National Science Foundation

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This study explores the molecular and neuronal mechanisms underlying the transition from feeding to courtship in Drosophila melanogaster. The results show that feeding is prioritized over courtship in starved males, but the consumption of protein-rich food rapidly reverses this order. A gut-derived neuropeptide hormone called Diuretic hormone 31 (Dh31) plays a role in switching from feeding to courtship. The findings also reveal that Dh31 stimulates specific brain neurons through the circulation, leading to the prioritization of courtship over feeding through parallel pathways.
Animals must set behavioural priority in a context-dependent manner and switch from one behaviour to another at the appropriate moment(1-3). Here we probe the molecular and neuronal mechanisms that orchestrate the transition from feeding to courtship in Drosophila melanogaster. We find that feeding is prioritized over courtship in starved males, and the consumption of protein-rich food rapidly reverses this order within a few minutes. At the molecular level, a gut-derived, nutrient-specific neuropeptide hormone-Diuretic hormone 31 (Dh31)-propels a switch from feeding to courtship. We further address the underlying kinetics with calcium imaging experiments. Amino acids from food acutely activate Dh31(+) enteroendocrine cells in the gut, increasing Dh31 levels in the circulation. In addition, three-photon functional imaging of intact flies shows that optogenetic stimulation of Dh31(+) enteroendocrine cells rapidly excites a subset of brain neurons that express Dh31 receptor (Dh31R). Gut-derived Dh31 excites the brain neurons through the circulatory system within a few minutes, in line with the speed of the feeding-courtship behavioural switch. At the circuit level, there are two distinct populations of Dh31R(+) neurons in the brain, with one population inhibiting feeding through allatostatin-C and the other promoting courtship through corazonin. Together, our findings illustrate a mechanism by which the consumption of protein-rich food triggers the release of a gut hormone, which in turn prioritizes courtship over feeding through two parallel pathways.

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