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 |
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Format: | Artikel |
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. |
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ISSN: | 0028-0836 1476-4687 |
DOI: | 10.1038/35065004 |