Opendata, web and dolomites

MicroCyFly SIGNED

Microcircuitry of the Drosophila visual system

Total Cost €

0

EC-Contrib. €

0

Partnership

0

Views

0

Project "MicroCyFly" data sheet

The following table provides information about the project.

Coordinator
JOHANNES GUTENBERG-UNIVERSITAT MAINZ 

Organization address
address: SAARSTRASSE 21
city: MAINZ
postcode: 55122
website: www.uni-mainz.de

contact info
title: n.a.
name: n.a.
surname: n.a.
function: n.a.
email: n.a.
telephone: n.a.
fax: n.a.

 Coordinator Country Germany [DE]
 Total cost 1˙497˙712 €
 EC max contribution 1˙497˙712 € (100%)
 Programme 1. H2020-EU.1.1. (EXCELLENT SCIENCE - European Research Council (ERC))
 Code Call ERC-2016-STG
 Funding Scheme ERC-STG
 Starting year 2017
 Duration (year-month-day) from 2017-07-01   to  2022-06-30

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    JOHANNES GUTENBERG-UNIVERSITAT MAINZ DE (MAINZ) coordinator 1˙196˙163.00
2    UNIVERSITAETSMEDIZIN GOETTINGEN - GEORG-AUGUST-UNIVERSITAET GOETTINGEN - STIFTUNG OEFFENTLICHEN RECHTS DE (GOETTINGEN) participant 301˙548.00

Map

 Project objective

Neural networks process sensory inputs into outputs that guide behavioral responses. The computations that take place can be complex, suggesting intricate circuit architecture. While we are starting to unravel the circuit components of a specific neural computation, the extraction of visual motion cues, we realize that the circuits are more complex than anticipated. Here, we aim to reveal the full microcircuitry of behaviorally relevant motion-detecting pathways with complex physiological properties. To understand the network implementation of a critical computation, we are studying motion detection in Drosophila. A hallmark is the extraction of direction-selective (DS) signals, which is achieved by spatiotemporal correlations of inputs. Neurons that are sufficient to set up DS signals have been identified, but are often not behaviorally necessary, suggesting redundant circuits at minimum. We have isolated a core visual pathway that is required for behavioral responses to motion cues, but displays physiological properties that are not in line with current models of motion detection. Recent data also show that DS neurons have complex receptive fields. Further, single neuronal inputs feed into both ON and OFF pathways, which later converge to control the behavioral output. What are the microcircuits that shape such receptive fields? And how do individual neurons, or individual synaptic connections contribute to one specific pathway and what is their specific computational role? We will dissect how complex receptive field properties and behavior are shaped by individual neurons. Further, we will develop a new tool to conditionally inactivate specific synaptic connection, Flp-TEV. This will allow to determine how individual synapses contribute to distinct downstream circuit properties, and behavior. We are thus proposing to map the circuit architecture of a behaviorally relevant visual pathway and understand how complex microcircuits perform relevant computation

Are you the coordinator (or a participant) of this project? Plaese send me more information about the "MICROCYFLY" project.

For instance: the website url (it has not provided by EU-opendata yet), the logo, a more detailed description of the project (in plain text as a rtf file or a word file), some pictures (as picture files, not embedded into any word file), twitter account, linkedin page, etc.

Send me an  email (fabio@fabiodisconzi.com) and I put them in your project's page as son as possible.

Thanks. And then put a link of this page into your project's website.

The information about "MICROCYFLY" are provided by the European Opendata Portal: CORDIS opendata.

More projects from the same programme (H2020-EU.1.1.)

CohoSing (2019)

Cohomology and Singularities

Read More  

PROTECHT (2020)

Providing RObust high TECHnology Tags based on linear carbon nanostructures

Read More  

Neuro-UTR (2019)

Mechanism and functional impact of ultra-long 3’ UTRs in the Drosophila nervous system

Read More