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The genetic network downstream of tcf mediated Wnt/beta-catenin signaling during the establishment of brain asymmetries

Antragsteller Dr. Matthias Carl
Fachliche Zuordnung Entwicklungsbiologie
Förderung Förderung von 2011 bis 2016
Projektkennung Deutsche Forschungsgemeinschaft (DFG) - Projektnummer 207735088
 
Erstellungsjahr 2016

Zusammenfassung der Projektergebnisse

With the help from the DFG, we have reached several milestones to understand asymmetric brain development and function. On the molecular level, we have identified the Wnt signaling molecule Tcf7l2 as a key regulator of all habenular neuronal types and habenular asymmetry. On the network level, we have uncovered the previously unknown origin of the ventral habenula. Furthermore, the development of novel tools and an unprecedented in vivo imaging assay in combination with focal laser ablations allowed us to unravel a novel mechanism of neural network development. On the functional level, we have established an amenable brain structure as a model to study the functional importance of neuroanatomical asymmetries. Our work has opened the field for further investigations on all three levels. The conserved habenular neurotransmittersystem is a central regulator of various behaviors and has been implicated to play a key role in the pathophysiology of depression and schizophrenia. Therefore, it will be intriguing to further translate our findings into the medical field.

Projektbezogene Publikationen (Auswahl)

 
 

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