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Neural Mechanisms of Action-Selection During Sensory Conflict

Project description

Neuronal mechanisms of selecting an appropriate action

Neuronal mechanisms of action selection, or how the brain evaluates sensory conflicting options and selects an appropriate action, remains unknown. The EU-funded CourtEscape project aims to study neural mechanisms that govern the selection between competing options. Researchers will develop a novel assay where Drosophila fruit fly males will be confronted with visual threats during mating creating a conflict between survival and reproduction. The objective is to identify neurons whose involvement prevents males from blocking courtship in response to the threat, using optogenetic tools in combination with a behavioural screen. The ultimate goal of the project is to build a map of the neural network of action selection.

Objective

Prioritising the most urgent goal according to the context and physiological needs is crucial for the success of any organism. Action-selection processes are often disrupted in neuropathologies, such as Parkinson's disease, Alzheimer's disease and addiction; however, the underlying neuronal mechanisms are not well understood. Crucially, how the brain evaluates sensory conflicting options and selects an appropriate action remains unknown. I will tackle this question using a novel assay in which Drosophila fruit fly males are confronted with visual threats during courtship, which creates a conflict between survival and reproduction. Capitalising on refined genetic tools, I aim to unravel neural mechanisms that govern the selection between competing options. I will carry out a behavioural screen to identify neurons that allow the fly to choose between courting a mate and escaping a threat. From an in silico screen of Gal4 fly lines targeting defined cells, I will select lines based on their potential connectivity with courtship-command neurons. Using optogenetic tools, I will identify neurons that, when activated or inhibited, prevent males from blocking courtship in response to the threat. Next, I will ask if these cells respond to the threat in live Ca2+ imaging studies, and test if they are linked with the courtship circuitry using pre and post-synaptic markers and GRASP (to test potential synaptic connections). To probe if candidate neurons are functionally linked, I will manipulate the activity of upstream cells, and test the responses in downstream cells with Ca2+ imaging. This will allow me to build a map of the neural network of action-selection. Finally, I will test how external and internal state variables modulate action-selection. This study will provide insights into fundamental brain processes that may work in other animals, including humans.

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MSCA-IF - Marie Skłodowska-Curie Individual Fellowships (IF)

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Call for proposal

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(opens in new window) H2020-MSCA-IF-2020

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Coordinator

THE UNIVERSITY OF BIRMINGHAM
Net EU contribution

Net EU financial contribution. The sum of money that the participant receives, deducted by the EU contribution to its linked third party. It considers the distribution of the EU financial contribution between direct beneficiaries of the project and other types of participants, like third-party participants.

€ 212 933,76
Address
Edgbaston
B15 2TT Birmingham
United Kingdom

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Region
West Midlands (England) West Midlands Birmingham
Activity type
Higher or Secondary Education Establishments
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Total cost

The total costs incurred by this organisation to participate in the project, including direct and indirect costs. This amount is a subset of the overall project budget.

€ 212 933,76
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