A third member of the synapsin gene family

  1. Hung-Teh Kao*,,,§,
  2. Barbara Porton*,,
  3. Andrew J. Czernik*,
  4. Jian Feng*,
  5. Glenn Yiu*,
  6. Monika Häring*,
  7. Fabio Benfenati, and
  8. Paul Greengard*
  1. *Laboratory of Molecular and Cellular Neuroscience, The Rockefeller University, 1230 York Avenue, New York, NY 10021-6399; Department of Psychiatry, Cornell University Medical College, 525 East 68th Street, New York, NY 10021-4899; and Department of Neuroscience, University of Roma Tor Vergata, Via di Tor Vergata 135, 00133 Roma, Italy
  1. Contributed by Paul Greengard

Abstract

Synapsins are a family of neuron-specific synaptic vesicle-associated phosphoproteins that have been implicated in synaptogenesis and in the modulation of neurotransmitter release. In mammals, distinct genes for synapsins I and II have been identified, each of which gives rise to two alternatively spliced isoforms. We have now cloned and characterized a third member of the synapsin gene family, synapsin III, from human DNA. Synapsin III gives rise to at least one protein isoform, designated synapsin IIIa, in several mammalian species. Synapsin IIIa is associated with synaptic vesicles, and its expression appears to be neuron-specific. The primary structure of synapsin IIIa conforms to the domain model previously described for the synapsin family, with domains A, C, and E exhibiting the highest degree of conservation. Synapsin IIIa contains a novel domain, termed domain J, located between domains C and E. The similarities among synapsins I, II, and III in domain organization, neuron-specific expression, and subcellular localization suggest a possible role for synapsin III in the regulation of neurotransmitter release and synaptogenesis. The human synapsin III gene is located on chromosome 22q12–13, which has been identified as a possible schizophrenia susceptibility locus. On the basis of this localization and the well established neurobiological roles of the synapsins, synapsin III represents a candidate gene for schizophrenia.

Footnotes

  • H.-T.K. and B.P. were equal contributors.

  • § To whom reprint requests should be addressed at: The Rockefeller University, 1230 York Avenue, Box 296, New York, NY 10021-6399. e-mail: kaoh{at}rockvax.rockefeller.edu.

  • Data deposition: The sequence reported in this paper has been deposited in the GenBank database (accession no. AF046873).

  • ABBREVIATIONS:
    CaM K,
    Ca2+/calmodulin-dependent protein kinase;
    UTR,
    untranslated region
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