Skip to main content
Biochemical Journal logoLink to Biochemical Journal
. 1997 Jan 1;321(Pt 1):151–156. doi: 10.1042/bj3210151

Novel isoform of syntaxin 1 is expressed in mammalian cells.

M N Jagadish 1, J T Tellam 1, S L Macaulay 1, K H Gough 1, D E James 1, C W Ward 1
PMCID: PMC1218049  PMID: 9003414

Abstract

Syntaxin 1A has been identified previously as a neural-cell-specific, membrane-anchored receptor protein required for docking and fusion of synaptic vesicles with the presynaptic plasma membrane. Syntaxin 1A consists of 288 amino acid residues including a 265-residue N-terminal region exposed to the cytoplasm and a C-terminal hydrophobic stretch of 23 residues believed to anchor syntaxin to the plasma membrane. Using a human fat-cell library we have isolated a novel cDNA clone of syntaxin 1A containing an insert of 91 bp in codon 226. This insert and subsequent frame shift generated a cDNA that codes for a truncated protein of 260 residues without the C-terminal transmembrane domain characteristic of the syntaxin family. Analysis of the deduced amino acid sequence of the new cDNA clone, termed syntaxin 1C, showed that it was identical for the first 226 residues with the previously described neural syntaxin 1A, and diverged thereafter. The truncated protein lacked the botulinum neurotoxin C cleavage site (Lys253-Ala254), a feature of the syntaxin 1A protein, because of the novel C-terminal domain of 34 residues. The new C-terminal region contained a single cysteine residue and was moderately rich in proline, with three repeats of a PXP motif. The insert occurred within the region encoding the coiled-coil motifs required for interactions with synaptobrevin, alpha-SNAP (SNAP being soluble N-ethylmaleimide-sensitive factor attachment protein) and n-Sec1/Munc-18 (n-Sec1 being the rat brain homologue of yeast Sec1p and Munc-18 the mammalian homologue of Caenorhabditis elegans unc-18, but five residues outside the domain previously mapped as being required for binding SNAP-25. Interaction studies in vitro suggested that unlike syntaxin 1A, which binds to both Munc-18a and- 18b, syntaxin 1C binds only to Munc-18b. The new isoform syntaxin 1C, which might be generated by alternative splicing of the syntaxin 1 gene, was expressed in several human tissues, including brain. Immuno-precipitation and immunoblotting with the monoclonal antibody HPC-1 and a polyclonal antibody raised against a peptide corresponding to the unique C-terminal 35 residues of syntaxin 1C failed to detect syntaxin 1C at the protein level in extracts of muscle, fat or brain.

Full Text

The Full Text of this article is available as a PDF (337.5 KB).

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Aalto M. K., Ronne H., Keränen S. Yeast syntaxins Sso1p and Sso2p belong to a family of related membrane proteins that function in vesicular transport. EMBO J. 1993 Nov;12(11):4095–4104. doi: 10.1002/j.1460-2075.1993.tb06093.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Bassham D. C., Gal S., da Silva Conceiço A., Raikhel N. V. An Arabidopsis syntaxin homologue isolated by functional complementation of a yeast pep12 mutant. Proc Natl Acad Sci U S A. 1995 Aug 1;92(16):7262–7266. doi: 10.1073/pnas.92.16.7262. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Bennett M. K., Calakos N., Scheller R. H. Syntaxin: a synaptic protein implicated in docking of synaptic vesicles at presynaptic active zones. Science. 1992 Jul 10;257(5067):255–259. doi: 10.1126/science.1321498. [DOI] [PubMed] [Google Scholar]
  4. Bennett M. K., García-Arrarás J. E., Elferink L. A., Peterson K., Fleming A. M., Hazuka C. D., Scheller R. H. The syntaxin family of vesicular transport receptors. Cell. 1993 Sep 10;74(5):863–873. doi: 10.1016/0092-8674(93)90466-4. [DOI] [PubMed] [Google Scholar]
  5. Blasi J., Chapman E. R., Yamasaki S., Binz T., Niemann H., Jahn R. Botulinum neurotoxin C1 blocks neurotransmitter release by means of cleaving HPC-1/syntaxin. EMBO J. 1993 Dec;12(12):4821–4828. doi: 10.1002/j.1460-2075.1993.tb06171.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Chapman E. R., An S., Barton N., Jahn R. SNAP-25, a t-SNARE which binds to both syntaxin and synaptobrevin via domains that may form coiled coils. J Biol Chem. 1994 Nov 4;269(44):27427–27432. [PubMed] [Google Scholar]
  7. De Camilli P. The eighth Datta Lecture. Molecular mechanisms in synaptic vesicle recycling. FEBS Lett. 1995 Aug 1;369(1):3–12. doi: 10.1016/0014-5793(95)00739-v. [DOI] [PubMed] [Google Scholar]
  8. Harrison S. D., Broadie K., van de Goor J., Rubin G. M. Mutations in the Drosophila Rop gene suggest a function in general secretion and synaptic transmission. Neuron. 1994 Sep;13(3):555–566. doi: 10.1016/0896-6273(94)90025-6. [DOI] [PubMed] [Google Scholar]
  9. Hata Y., Slaughter C. A., Südhof T. C. Synaptic vesicle fusion complex contains unc-18 homologue bound to syntaxin. Nature. 1993 Nov 25;366(6453):347–351. doi: 10.1038/366347a0. [DOI] [PubMed] [Google Scholar]
  10. Hata Y., Südhof T. C. A novel ubiquitous form of Munc-18 interacts with multiple syntaxins. Use of the yeast two-hybrid system to study interactions between proteins involved in membrane traffic. J Biol Chem. 1995 Jun 2;270(22):13022–13028. doi: 10.1074/jbc.270.22.13022. [DOI] [PubMed] [Google Scholar]
  11. Hayashi T., McMahon H., Yamasaki S., Binz T., Hata Y., Südhof T. C., Niemann H. Synaptic vesicle membrane fusion complex: action of clostridial neurotoxins on assembly. EMBO J. 1994 Nov 1;13(21):5051–5061. doi: 10.1002/j.1460-2075.1994.tb06834.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Hirai Y. Molecular cloning of human epimorphin: identification of isoforms and their unique properties. Biochem Biophys Res Commun. 1993 Mar 31;191(3):1332–1337. doi: 10.1006/bbrc.1993.1363. [DOI] [PubMed] [Google Scholar]
  13. Hosono R., Hekimi S., Kamiya Y., Sassa T., Murakami S., Nishiwaki K., Miwa J., Taketo A., Kodaira K. I. The unc-18 gene encodes a novel protein affecting the kinetics of acetylcholine metabolism in the nematode Caenorhabditis elegans. J Neurochem. 1992 Apr;58(4):1517–1525. doi: 10.1111/j.1471-4159.1992.tb11373.x. [DOI] [PubMed] [Google Scholar]
  14. Ibaraki K., Horikawa H. P., Morita T., Mori H., Sakimura K., Mishina M., Saisu H., Abe T. Identification of four different forms of syntaxin 3. Biochem Biophys Res Commun. 1995 Jun 26;211(3):997–1005. doi: 10.1006/bbrc.1995.1910. [DOI] [PubMed] [Google Scholar]
  15. Inoue A., Obata K., Akagawa K. Cloning and sequence analysis of cDNA for a neuronal cell membrane antigen, HPC-1. J Biol Chem. 1992 May 25;267(15):10613–10619. [PubMed] [Google Scholar]
  16. Jacobsson G., Bean A. J., Scheller R. H., Juntti-Berggren L., Deeney J. T., Berggren P. O., Meister B. Identification of synaptic proteins and their isoform mRNAs in compartments of pancreatic endocrine cells. Proc Natl Acad Sci U S A. 1994 Dec 20;91(26):12487–12491. doi: 10.1073/pnas.91.26.12487. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Jagadish M. N., Fernandez C. S., Hewish D. R., Macaulay S. L., Gough K. H., Grusovin J., Verkuylen A., Cosgrove L., Alafaci A., Frenkel M. J. Insulin-responsive tissues contain the core complex protein SNAP-25 (synaptosomal-associated protein 25) A and B isoforms in addition to syntaxin 4 and synaptobrevins 1 and 2. Biochem J. 1996 Aug 1;317(Pt 3):945–954. doi: 10.1042/bj3170945. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Katagiri H., Terasaki J., Murata T., Ishihara H., Ogihara T., Inukai K., Fukushima Y., Anai M., Kikuchi M., Miyazaki J. A novel isoform of syntaxin-binding protein homologous to yeast Sec1 expressed ubiquitously in mammalian cells. J Biol Chem. 1995 Mar 10;270(10):4963–4966. doi: 10.1074/jbc.270.10.4963. [DOI] [PubMed] [Google Scholar]
  19. Kee Y., Lin R. C., Hsu S. C., Scheller R. H. Distinct domains of syntaxin are required for synaptic vesicle fusion complex formation and dissociation. Neuron. 1995 May;14(5):991–998. doi: 10.1016/0896-6273(95)90337-2. [DOI] [PubMed] [Google Scholar]
  20. Koh S., Yamamoto A., Inoue A., Inoue Y., Akagawa K., Kawamura Y., Kawamoto K., Tashiro Y. Immunoelectron microscopic localization of the HPC-1 antigen in rat cerebellum. J Neurocytol. 1993 Nov;22(11):995–1005. doi: 10.1007/BF01218356. [DOI] [PubMed] [Google Scholar]
  21. Kutay U., Ahnert-Hilger G., Hartmann E., Wiedenmann B., Rapoport T. A. Transport route for synaptobrevin via a novel pathway of insertion into the endoplasmic reticulum membrane. EMBO J. 1995 Jan 16;14(2):217–223. doi: 10.1002/j.1460-2075.1995.tb06994.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Li C., Ullrich B., Zhang J. Z., Anderson R. G., Brose N., Südhof T. C. Ca(2+)-dependent and -independent activities of neural and non-neural synaptotagmins. Nature. 1995 Jun 15;375(6532):594–599. doi: 10.1038/375594a0. [DOI] [PubMed] [Google Scholar]
  23. Pevsner J., Hsu S. C., Scheller R. H. n-Sec1: a neural-specific syntaxin-binding protein. Proc Natl Acad Sci U S A. 1994 Feb 15;91(4):1445–1449. doi: 10.1073/pnas.91.4.1445. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Rothman J. E. Mechanisms of intracellular protein transport. Nature. 1994 Nov 3;372(6501):55–63. doi: 10.1038/372055a0. [DOI] [PubMed] [Google Scholar]
  25. Schiavo G., Shone C. C., Bennett M. K., Scheller R. H., Montecucco C. Botulinum neurotoxin type C cleaves a single Lys-Ala bond within the carboxyl-terminal region of syntaxins. J Biol Chem. 1995 May 5;270(18):10566–10570. doi: 10.1074/jbc.270.18.10566. [DOI] [PubMed] [Google Scholar]
  26. Schulze K. L., Broadie K., Perin M. S., Bellen H. J. Genetic and electrophysiological studies of Drosophila syntaxin-1A demonstrate its role in nonneuronal secretion and neurotransmission. Cell. 1995 Jan 27;80(2):311–320. doi: 10.1016/0092-8674(95)90414-x. [DOI] [PubMed] [Google Scholar]
  27. Sumitani S., Ramlal T., Liu Z., Klip A. Expression of syntaxin 4 in rat skeletal muscle and rat skeletal muscle cells in culture. Biochem Biophys Res Commun. 1995 Aug 15;213(2):462–468. doi: 10.1006/bbrc.1995.2154. [DOI] [PubMed] [Google Scholar]
  28. Söllner T., Bennett M. K., Whiteheart S. W., Scheller R. H., Rothman J. E. A protein assembly-disassembly pathway in vitro that may correspond to sequential steps of synaptic vesicle docking, activation, and fusion. Cell. 1993 Nov 5;75(3):409–418. doi: 10.1016/0092-8674(93)90376-2. [DOI] [PubMed] [Google Scholar]
  29. Söllner T. SNAREs and targeted membrane fusion. FEBS Lett. 1995 Aug 1;369(1):80–83. doi: 10.1016/0014-5793(95)00594-y. [DOI] [PubMed] [Google Scholar]
  30. Söllner T., Whiteheart S. W., Brunner M., Erdjument-Bromage H., Geromanos S., Tempst P., Rothman J. E. SNAP receptors implicated in vesicle targeting and fusion. Nature. 1993 Mar 25;362(6418):318–324. doi: 10.1038/362318a0. [DOI] [PubMed] [Google Scholar]
  31. Südhof T. C. The synaptic vesicle cycle: a cascade of protein-protein interactions. Nature. 1995 Jun 22;375(6533):645–653. doi: 10.1038/375645a0. [DOI] [PubMed] [Google Scholar]
  32. Tagaya M., Toyonaga S., Takahashi M., Yamamoto A., Fujiwara T., Akagawa K., Moriyama Y., Mizushima S. Syntaxin 1 (HPC-1) is associated with chromaffin granules. J Biol Chem. 1995 Jul 7;270(27):15930–15933. doi: 10.1074/jbc.270.27.15930. [DOI] [PubMed] [Google Scholar]
  33. Tellam J. T., McIntosh S., James D. E. Molecular identification of two novel Munc-18 isoforms expressed in non-neuronal tissues. J Biol Chem. 1995 Mar 17;270(11):5857–5863. doi: 10.1074/jbc.270.11.5857. [DOI] [PubMed] [Google Scholar]
  34. Walch-Solimena C., Blasi J., Edelmann L., Chapman E. R., von Mollard G. F., Jahn R. The t-SNAREs syntaxin 1 and SNAP-25 are present on organelles that participate in synaptic vesicle recycling. J Cell Biol. 1995 Feb;128(4):637–645. doi: 10.1083/jcb.128.4.637. [DOI] [PMC free article] [PubMed] [Google Scholar]
  35. Yoshida A., Oho C., Omori A., Kuwahara R., Ito T., Takahashi M. HPC-1 is associated with synaptotagmin and omega-conotoxin receptor. J Biol Chem. 1992 Dec 15;267(35):24925–24928. [PubMed] [Google Scholar]
  36. Zhang R., Maksymowych A. B., Simpson L. L. Cloning and sequence analysis of a cDNA encoding human syntaxin 1A, a polypeptide essential for exocytosis. Gene. 1995 Jul 4;159(2):293–294. doi: 10.1016/0378-1119(95)00152-v. [DOI] [PubMed] [Google Scholar]

Articles from Biochemical Journal are provided here courtesy of The Biochemical Society

RESOURCES