Literature DB >> 11444845

Identification of three new splice variants of the SNARE protein SNAP-23.

A Shukla1, T J Corydon, S Nielsen, H J Hoffmann, R Dahl.   

Abstract

SNAP-23 has an important role in protein-trafficking processes in mammalian cells and until yet two isoforms of SNAP-23 (SNAP-23a and SNAP-23b) have been described. In the present report, we have identified the existence of three new SNAP-23 isoforms (named SNAP-23c, SNAP-23d, and SNAP-23e), which arise from alternative splicing. By RT-PCR all five splice variants were shown to be expressed in four different human inflammatory cells (eosinophils, basophils, neutrophils, and peripheral blood mononuclear cells). Transfection of the human basophilic KU-812 cell line with plasmid constructs containing the cDNAs of the five splice variants located SNAP-23a and SNAP-23b primarily in the plasma membrane. The other three splice variants were localized both intracellularly and in the plasma membrane. Copyright 2001 Academic Press.

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Year:  2001        PMID: 11444845     DOI: 10.1006/bbrc.2001.5144

Source DB:  PubMed          Journal:  Biochem Biophys Res Commun        ISSN: 0006-291X            Impact factor:   3.575


  2 in total

Review 1.  How alternative splicing affects membrane-trafficking dynamics.

Authors:  R Eric Blue; Ennessa G Curry; Nichlas M Engels; Eunice Y Lee; Jimena Giudice
Journal:  J Cell Sci       Date:  2018-05-16       Impact factor: 5.285

2.  Alternative splicing of the human gene SYBL1 modulates protein domain architecture of Longin VAMP7/TI-VAMP, showing both non-SNARE and synaptobrevin-like isoforms.

Authors:  Marcella Vacca; Lara Albania; Floriana Della Ragione; Andrea Carpi; Valeria Rossi; Maria Strazzullo; Nicola De Franceschi; Ornella Rossetto; Francesco Filippini; Maurizio D'Esposito
Journal:  BMC Mol Biol       Date:  2011-05-24       Impact factor: 2.946

  2 in total

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