Synaptotagmin I functions as a calcium regulator of release probability

In all synapses, Ca 2+ triggers neurotransmitter release to initiate signal transmission. Ca 2+ presumably acts by activating synaptic Ca 2+ sensors, but the nature of these sensors—which are the gatekeepers to neurotransmission—remains unclear. One of the candidate Ca 2+ sensors in release is the s...

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Veröffentlicht in:Nature (London) 2001-03, Vol.410 (6824), p.41-49
Hauptverfasser: Fernández-Chacón, Rafael, Königstorfer, Andreas, Gerber, Stefan H., García, Jesús, Matos, Maria F., Stevens, Charles F., Brose, Nils, Rizo, Josep, Rosenmund, Christian, Südhof, Thomas C.
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Sprache:eng
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Zusammenfassung:In all synapses, Ca 2+ triggers neurotransmitter release to initiate signal transmission. Ca 2+ presumably acts by activating synaptic Ca 2+ sensors, but the nature of these sensors—which are the gatekeepers to neurotransmission—remains unclear. One of the candidate Ca 2+ sensors in release is the synaptic Ca 2+ -binding protein synaptotagmin I. Here we have studied a point mutation in synaptotagmin I that causes a twofold decrease in overall Ca 2+ affinity without inducing structural or conformational changes. When introduced by homologous recombination into the endogenous synaptotagmin I gene in mice, this point mutation decreases the Ca 2+ sensitivity of neurotransmitter release twofold, but does not alter spontaneous release or the size of the readily releasable pool of neurotransmitters. Therefore, Ca 2+ binding to synaptotagmin I participates in triggering neurotransmitter release at the synapse.
ISSN:0028-0836
1476-4687
DOI:10.1038/35065004