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Prof. Dr. Gaia Tavosanis
Kandidatin "Schatzmeisterin"
RWTH Aachen Tel.: (+49) 0221 80 20870 E-Mail: gaia.tavosanis@devbiol.rwth-aachen.de Lab Website: https://www.devbiol.rwth-aachen.de/prof-dr-gaia-tavosanis/ |
Curriculum Vitae |
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Scientific education
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| 1995-1999 | PhD student in the laboratory of Dr. C. Gonzalez, EMBL, Heidelberg, Germany |
| 1999 | Post-doctoral work in the laboratory of Dr. C. Gonzalez (EMBL- Cell Biology Postdoctoral Fellowship) |
| 2000-2002 | Post-doc in the laboratory of Prof. Dr. Yuh-Nung Jan, UCSF, San Francisco, CA, USA (DFG Postdoctoral Grant) |
| 2003-2011 | Junior Group Leader at the MPI of Neurobiology, Munich, Germany |
| 2011-2016 | Research Group Leader (W2 level) at the DZNE, Bonn, Germany |
| 2016-2022 | Research Group Leader (W3 level) at the DZNE, Bonn, Germany |
| 2017-2022 | Research Group Leader (W3 level) at the DZNE, Bonn |
| 2017-2022 | Full Professor of Neurogenetics (W3) at the University of Bonn |
| 2022-present | Full Professor, Chair of Developmental Biology (W3) at the RWTH Aachen |
My group investigates how architectural constrains in the nervous system define the processing of information- from the cellular to the circuit level. We implement high resolution imaging to investigate how dendrites differentiate in vivo and how they can be modified upon changes of sensory stimuli in the adult nervous system. We combine this microscopy approach with cutting-edge Drosophila genetics and molecular biology to investigate molecularly the cellular mechanisms of dendrite branching. Using these approaches, we have demonstrated that distinct molecular regulation of the cytoskeleton underlies the diversity of dendrite morphologies observed among neuronal types. Indeed, actin regulation and nucleation of microtubules both play a central role in our research, as major players in establishment and plasticity of cellular architecture. We postulate that same or similar molecular players are involved in the initial establishment and in the physiological dynamic remodelling of the adult nervous system. Therefore, we have identified and characterized circuits in the adult nervous system of Drosophila that allow us to address plastic changes and have demonstrated that developmental circuit assembly in Drosophila depends on modulation of input activity. To investigate the functional outcome of synaptic remodelling and of structural cellular modifications, we have established behavioural paradigms, including learning and memory essays, and have set up functional imaging using genetically encoded calcium indicators and two-photon microscopy. With these tools, we have reported circuit rewiring accompanying memory consolidation in the adult fly brain. Thus, we investigate the structural, molecular, functional and behavioural outcome of the nervous system plastic response to a modified environment.