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Synaptotagmin I: a major Ca2+ sensor for transmitter release at a central synapse.

Cell | Nov 18, 1994

Mice carrying a mutation in the synaptotagmin I gene were generated by homologous recombination. Mutant mice are phenotypically normal as heterozygotes, but die within 48 hr after birth as homozygotes. Studies of hippocampal neurons cultured from homozygous mutant mice reveal that synaptic transmission is severely impaired. The synchronous, fast component of Ca(2+)-dependent neurotransmitter release is decreased, whereas asynchronous release processes, including spontaneous synaptic activity (miniature excitatory postsynaptic current frequency) and release triggered by hypertonic solution or alpha-latrotoxin, are unaffected. Our findings demonstrate that synaptotagmin I function is required for Ca2+ triggering of synchronous neurotransmitter release, but is not essential for asynchronous or Ca(2+)-independent release. We propose that synaptotagmin I is the major low affinity Ca2+ sensor mediating Ca2+ regulation of synchronous neurotransmitter release in hippocampal neurons.

Pubmed ID: 7954835 RIS Download

Mesh terms: Animals | Animals, Newborn | Base Sequence | Brain | Calcium | Calcium-Binding Proteins | DNA Primers | Exons | Hippocampus | Homozygote | Hypertonic Solutions | Membrane Glycoproteins | Mice | Mice, Neurologic Mutants | Molecular Sequence Data | Mutagenesis | Mutation | Nerve Tissue Proteins | Neurons | Neurotransmitter Agents | Polymerase Chain Reaction | Reference Values | Restriction Mapping | Spider Venoms | Synapses | Synaptic Transmission | Synaptotagmin I | Synaptotagmins

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Associated grants

  • Agency: NINDS NIH HHS, Id: R0 NS 12961-17

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