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bioRxiv · 10.1101/2022.04.01.486686

Munc13 supports vesicle fusogenicity after disrupting active zone scaffolds and synaptic vesicle docking

Tan, C.·de Nola, G.·Qiao, C.·Imig, C.·Brose, N.·Kaeser, P. S.
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Abstract

Active zones consist of protein scaffolds that are tightly attached to the presynaptic plasma membrane. They dock and prime synaptic vesicles, couple them to Ca2+ entry, and target neurotransmitter release to postsynaptic receptor domains. Simultaneous RIM+ELKS ablation disrupts these scaffolds, abolishes vesicle docking and removes active zone-targeted Munc13, but some vesicles remain releasable. This enduring vesicular fusogenicity may be Munc13-independent or be mediated by non-active zone-anchored Munc13. We tested its Munc13-dependence by ablating Munc13-1 and Munc13-2 on top of RIM+ELKS in cultured hippocampal neurons. The hextuple knockout synapses lacked docked vesicles, but other ultrastructural features were near-normal despite the strong genetic manipulation. Removing Munc13 in addition to RIM+ELKS further impaired action potential-evoked release by decreasing the remaining pool of releasable vesicles. We conclude that Munc13 can support some fusogenicity without RIM and ELKS, and that presynaptic recruitment of Munc13, even without active zone-anchoring, suffices to generate some fusion-competent vesicles.

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Tan, C., de Nola, G., Qiao, C., Imig, C., Brose, N., Kaeser, P. S.. 2022-04-01. Munc13 supports vesicle fusogenicity after disrupting active zone scaffolds and synaptic vesicle docking. https://doi.org/10.1101/2022.04.01.486686

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