H2020Индивидуална стипендия2018–2020

sexual dimorphism · Sexually dimorphic neuronal circuits underlying social behaviours in Drosophila

„Хоризонт 2020“ — Действия „Мария Склодовска-Кюри“

Период
2018-09-01 → 2020-11-30
Финансиране от ЕС
195 455 €
Участници
1
Схема
MSCA-IF

Линиите свързват координатора с партньорите.

Накратко на български

Невронните вериги в мозъка на плодовите мухи се изследват, за да се разбере как един и същ феромон предизвиква различно поведение при мъжките и женските. Това помага да се разбере как генетично определените разлики в мозъка управляват социалните взаимодействия.

Този кратък обзор е генериран от изкуствен интелект

Кратко обяснение, генерирано от езиков модел по текста на CORDIS. Оригиналът е по-долу.

Резултати накратко

Sexually dimorphic neuronal circuits underlying social behaviours in Drosophila

Males and females show significant differences in social behaviours, which depend on sex-specific neuronal organization. These differences are critical for reproduction, parenting and other basic interactions between animals. However, the neural circuitry underlying sexually dimorphic patterns is mostly unknown. Sexually dimorphic behaviour in Drosophila is a key model system for revealing how genetically-determined properties of neuronal circuits define behaviour. Drosophila offers a unique model system to decipher the logic of dimorphic neuronal circuits, with its wealth of anatomical and neurogenetic tools, and a repertoire of dimorphic sexual behaviours. Although many sensory stimuli are integrated to regulate social behaviour, one of the best understood is the Drosophila male pheromone cVA, which promotes mating in females but repels other males and promotes inter-male aggression. Recent work from the host lab identified, for the first time, a sexually dimorphic switch in neuronal connectivity. The transcriptional master regulator fruitless rewires connections between pheromone responsive input neurons and two different target neuron populations in male and female brains. This study opened the question whether different target populations between males and females promote distinct behaviours. The current grant focused on three interdisciplinary aims that built on these results by establishing a causal role for specific wiring differences in regulating sexually dimorphic social behaviours; and studying how simple switches are assembled into more complex networks, at the interface of sensory processing and behavioural control. The main research questions were how is the pheromone processing pathway organized in male and female brains, and how do differences in this pathway between male and female affect sexual behaviour. Understanding the logic of sexually dimorphic circuits also teaches us how simple circuit motifs are assembled into complex networks, from sensory input to behavioural output. Conclusions of the action: Using the emerging Drosophila connectome (Figure 1A), we reconstructed the neuroanatomical map of brain connections in the pheromone processing circuitry. This neuroanatomical wiring map spans from sensory neurons (olfactory, gustatory and mechanical) to descending neurons controlling motor output. Based on the wiring map we identified five novel sets of neurons in key points transmitting pheromone information. We then identified genetic driver lines for each of these subsets, tested the functionality of the connectivity using functional imaging, and manipulated these neuronal subsets in the brain while flies were freely behaving, in both sexes. We uncovered how each neuronal subset contributes to dimorphic social behaviours, including male-male aggression, male-female courtship, female receptivity, and female egg laying. Our work provides a direct link between anatomical differences and functional differences, and pinpoint the roles of specific circuit elements in regulating sexual behaviours.

Текст от CORDIS, на английски · Данни: CORDIS, © Европейски съюз

Цел на проекта

Sex differences are basic for reproduction, parenting and other social interactions. Pheromone secretions that are differentially perceived by males and females, release stereotypical behaviours in many species. I will study how simple connectivity switches in a Drosophila sexually-dimorphic neuronal circuit are assembled into complex networks, from sensory processing to behavioural control. 11-cis-Vaccenyl-acetate (cVA) is a male-pheromone eliciting sex-specific responses: attracts females and repels males. Sex-specific wiring of olfactory neurons reroutes cVA information, forming a developmental switch in information flow. Central aSP-g neurons receive cVA innervation in females but not males, while this cluster is implicated in male-male aggressive behaviour. The role of aSP-g in social interactions was not compared between sexes, and that is my first aim. Next, I will find input and output neurons of aSP-g neurons in both sexes, by combining state-of-the-art anatomical, physiological and behavioural methodology: in-silico circuit-tracing methods to find neurons with overlapping innervations to aSP-g; and a unique electron-microscopy volume scan of a female brain to reconstruct aSP-g neurons and their synaptic partners. I will validate functional connectivity using photoactivation of output neurons while calcium-imaging target neurons. I aim to discover how sexually-specific wiring differences in homologous circuits regulate sexually-dimorphic social behaviours. These basic neuronal connectivity motifs may be conserved beyond flies.

Оригинален текст от CORDIS (на английски).

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Връзки

Данни: CORDIS, © Европейски съюз