Summary
A hallmark of the nervous system is its rich cell-type diversity, its intricate connectivity and its coordinated patterns of activity. Behavior largely is an emergent property of this complexity. Thus, to understand behavior, we must define neurons’ molecular, cellular and functional properties. This task has proven especially challenging for motor circuits with their readily apparent output in motor activity but astonishingly heterogeneous populations of neurons. To parse this complexity, I propose a novel approach harnessing the unique behavioral switch during Xenopus frog metamorphosis. The metamorphic transition from simple swimming to more complex, coordinated limb movement offers an ideal opportunity to study the expansion and diversification of two motor circuits in one organism. Here, I aim to define the molecular, functional and behavioral features of swim2limb circuit complexification during frog metamorphosis— a crucial step in developing this new model (Aim 1: OBSERVE). Next, I will identify the developmental mechanisms that drive the profound change in circuit composition and output, and evaluate the contribution of increasing cellular heterogeneity to pre- and post-metamorphic neuron activity and behavior (Aim 2: PERTURB). Finally, to define the conserved and divergent circuit features for swimming and walking across evolution, I will expand to a cross-species approach comparing frogs/mice and fish/tadpoles (Aim 3: COMPARE). Such intra- and inter- species approaches will deepen our understanding of the origin of tetrapod motor complexity and its relationship to motor circuit composition and output. My work will be the first comprehensive study of the genetics, activity, and behavior of a swim-to-limb transition in a single organism. It will draw bridges between studies of motor control from different species and generate hypotheses and knowledge for understanding motor circuit development, function, and dysfunction all the way to a clinical setting.
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| Web resources: | https://cordis.europa.eu/project/id/101041551 |
| Start date: | 01-09-2022 |
| End date: | 31-08-2027 |
| Total budget - Public funding: | 1 500 000,00 Euro - 1 500 000,00 Euro |
Cordis data
Original description
A hallmark of the nervous system is its rich cell-type diversity, its intricate connectivity and its coordinated patterns of activity. Behavior largely is an emergent property of this complexity. Thus, to understand behavior, we must define neurons’ molecular, cellular and functional properties. This task has proven especially challenging for motor circuits with their readily apparent output in motor activity but astonishingly heterogeneous populations of neurons. To parse this complexity, I propose a novel approach harnessing the unique behavioral switch during Xenopus frog metamorphosis. The metamorphic transition from simple swimming to more complex, coordinated limb movement offers an ideal opportunity to study the expansion and diversification of two motor circuits in one organism. Here, I aim to define the molecular, functional and behavioral features of swim2limb circuit complexification during frog metamorphosis— a crucial step in developing this new model (Aim 1: OBSERVE). Next, I will identify the developmental mechanisms that drive the profound change in circuit composition and output, and evaluate the contribution of increasing cellular heterogeneity to pre- and post-metamorphic neuron activity and behavior (Aim 2: PERTURB). Finally, to define the conserved and divergent circuit features for swimming and walking across evolution, I will expand to a cross-species approach comparing frogs/mice and fish/tadpoles (Aim 3: COMPARE). Such intra- and inter- species approaches will deepen our understanding of the origin of tetrapod motor complexity and its relationship to motor circuit composition and output. My work will be the first comprehensive study of the genetics, activity, and behavior of a swim-to-limb transition in a single organism. It will draw bridges between studies of motor control from different species and generate hypotheses and knowledge for understanding motor circuit development, function, and dysfunction all the way to a clinical setting.Status
SIGNEDCall topic
ERC-2021-STGUpdate Date
09-02-2023
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