Fife organizes synaptic vesicles and calcium channels for high-probability neurotransmitter release

Author:

Bruckner Joseph J.1ORCID,Zhan Hong2ORCID,Gratz Scott J.2ORCID,Rao Monica1,Ukken Fiona2,Zilberg Gregory2ORCID,O’Connor-Giles Kate M.123ORCID

Affiliation:

1. Cell and Molecular Biology Training Program, University of Wisconsin-Madison, Madison, WI 53706

2. Laboratory of Cell and Molecular Biology, University of Wisconsin-Madison, Madison, WI 53706

3. Laboratory of Genetics, University of Wisconsin-Madison, Madison, WI 53706

Abstract

The strength of synaptic connections varies significantly and is a key determinant of communication within neural circuits. Mechanistic insight into presynaptic factors that establish and modulate neurotransmitter release properties is crucial to understanding synapse strength, circuit function, and neural plasticity. We previously identified Drosophila Piccolo-RIM-related Fife, which regulates neurotransmission and motor behavior through an unknown mechanism. Here, we demonstrate that Fife localizes and interacts with RIM at the active zone cytomatrix to promote neurotransmitter release. Loss of Fife results in the severe disruption of active zone cytomatrix architecture and molecular organization. Through electron tomographic and electrophysiological studies, we find a decrease in the accumulation of release-ready synaptic vesicles and their release probability caused by impaired coupling to Ca2+ channels. Finally, we find that Fife is essential for the homeostatic modulation of neurotransmission. We propose that Fife organizes active zones to create synaptic vesicle release sites within nanometer distance of Ca2+ channel clusters for reliable and modifiable neurotransmitter release.

Funder

National Institutes of Health

McKnight Foundation

National Science Foundation

University of Wisconsin-Madison

Publisher

Rockefeller University Press

Subject

Cell Biology

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