Monday 4 June 2018, 1.00PM
Speaker(s): Prof Stephan Sigrist, Free University Berlin
Recently, high throughput electron microscopy has started to reveal complete wiring diagrams of single circuits and whole brain regions, for example in the Drosophila olfactory sensory and learning center. However, efficacy, timing, and frequency tuning of synaptic vesicle release are highly diversified across the development of brain circuitry. Systematic knowledge regarding the functional features of synapse types will be required for a satisfactory understanding and functional modeling of neural circuits. Using light superresolution microscopy, we provide evidence that presynaptic active zone scaffold protein diversity controls functional diversity across Drosophila brain synapses: distinct patterns of scaffold complexes differentially recruit specific Unc13 isoforms to steer transmission dynamics in a neuron-specific manner by conferring diverse nanometer-precise positioning of vesicle release sites to Ca2+ channels. In this manner, a compositional code of such stereotypic release modules diversifies synapse response properties. Our analysis provides ‘nanoscopic molecular fingerprints’ of synapse types which helps in understanding specific synaptic features in circuit modeling.
1. Fulterer A, Andlauer TFM, Ender A, et al. Active Zone Scaffold Protein Ratios Tune Functional Diversity across Brain Synapses. Cell reports 2018;23:1259-74.
2. Bohme MA, Beis C, Reddy-Alla S, et al. Active zone scaffolds differentially accumulate Unc13 isoforms to tune Ca(2+) channel-vesicle coupling. Nature neuroscience 2016;19:1311-20.
1 Freie Universität Berlin, Institute for Biology/Genetics, Takustrasse 6, 14195 Berlin, Germany
2 NeuroCure, Charité, Charitéplatz 1, 10117 Berlin, Germany