Abstract

Many animals adjust their reproductive behavior according to nutritional state and food availability. Drosophila females for instance decrease their sexual receptivity following starvation. Insulin signaling, which regulates many aspects of insect physiology and behavior, also affects reproduction in females. We show that insulin signaling is involved in the starvation-induced reduction in female receptivity. More specifically, females mutant for the insulin-like peptide 5 (dilp5) were less affected by starvation compared to the other dilp mutants and wild-type flies. Knocking-down the insulin receptor, either in all fruitless-positive neurons or a subset of these neurons dedicated to the perception of a male aphrodisiac pheromone, decreased the effect of starvation on female receptivity. Disrupting insulin signaling in some parts of the brain, including the mushroom bodies even abolished the effect of starvation. In addition, we identified fruitless-positive neurons in the dorso-lateral protocerebrum and in the mushroom bodies co-expressing the insulin receptor. Together, our results suggest that the interaction of insulin peptides determines the tuning of female sexual behavior, either by acting on pheromone perception or directly in the central nervous system.

Highlights

  • Adjusting reproductive behavior to nutrient availability is a common feature in many animals

  • We found that female sexual receptivity was significantly reduced after a period of starvation

  • Several insulin peptides produced in specific spatiotemporal patterns acting through one single receptor enables a fine-scale regulation of behaviors in response to changes in physiology

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Summary

Introduction

Adjusting reproductive behavior to nutrient availability is a common feature in many animals. Females of many animal species decrease their sexual receptivity to male courtship in response to food deprivation (Kauffman and Rissman, 2004; Pierce et al, 2007; Franssen et al, 2008; Lebreton et al, 2015). Mating modifies food preference in females (Carvalho et al, 2006; Walker et al, 2015) while feeding regulates their mating behavior (Lebreton et al, 2015, 2016). The molecular mechanisms regulating feeding behavior after mating are fairly well described and involve the transfer of a male component during copulation called Sex Peptide (Carvalho et al, 2006; Ribeiro and Dickson, 2010; Walker et al, 2015). The mechanisms by which feeding and starvation regulate sexual receptivity remain unknown

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