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Neural arithmetic of motion vision

Project description

Molecular insight into neuronal signal processing

Neurons possess the remarkable capacity to transform synaptic signals in a nonlinear fashion, a phenomenon that accounts for much of the brain’s computational power. However, little is known about the molecular mechanisms that allow a neuron to multiply or divide its input signals. Scientists of the EU-funded MOVIS project will use the motion vision circuit of the fruit fly Drosophila as a model system to address these problems. Drosophila constitutes an ideal model since the synaptic connectivity and the transcriptional activity of its nervous system are well characterised, and it can be manipulated and studied using molecular, biophysical, and behavioural methodologies. The project's work will provide a detailed mechanistic understanding of signal processing by single neurons.

Objective

Signal processing by neurons involves arithmetic operations, many of which are nonlinear. These nonlinearities are thought to account for much of the brain’s computational power, yet, little is known about the molecular mechanics that underlie even simple operations like multiplication and division in individual neurons. I will address this problem in the visual system of Drosophila, where the detection of motion represents a canonical example of nonlinear information processing: To perceive visual motion, the signals of adjacent photoreceptors are differentially delayed to coincide at the dendrites of the bushy T-cells, T4 and T5, where multiplication and/or division of these inputs are thought to give rise to direction selectivity. The proposed work will address the following questions: Are the dendritic transformations multiplicative, divisive, or both? Which synaptic inputs constitute the numerator and which the denominator? What receptors and ion channels account for the dendritic nonlinearities and how do they influence the visual perception of motion? The fruit fly enables me to bridge molecular biophysics and optomotor behaviour by granting genetic, electrical, optical, and molecular access to virtually all relevant neurons in a circuit of well-documented synaptic connectivity and transcriptional activity. I will use whole-cell patch clamp recordings in vivo, patch-seq, optogenetics, optomotor behaviour, RNA interference, and computational modelling to identify the biophysical basis of multiplicative and divisive operations in the dendrites of bushy T-cells. The answers will likely hold information that extends beyond the fly’s sense of sight and might uncover previously unknown ways of signal processing by single neurons at the molecular scale.

Fields of science (EuroSciVoc)

Keywords

Programme(s)

Topic(s)

Funding Scheme

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

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Call for proposal

(opens in new window) H2020-MSCA-IF-2019

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Coordinator

MAX-PLANCK-GESELLSCHAFT ZUR FORDERUNG DER WISSENSCHAFTEN EV
Net EU contribution
€ 174 806,40
Address
HOFGARTENSTRASSE 8
80539 MUNCHEN
Germany
Region
Berlin Berlin Berlin
Activity type
Research Organisations
Links
Total cost
€ 174 806,40