

FOLLOWUS
1. Institute of Oceanology Chinese Academy of Sciences
2. The First Institute of Oceanography State Oceanic Administration
3. Graduate University Chinese Academy of Sciences
4. Department of Physiology University of Toronto
纸质出版:2007
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Characterization of SNAP-25 gene from marine teleostean, Lateolabrax japonicus[J]. 海洋湖沼学报(英文), 2007,25(4):378-385.
Chen, K., Huang, X., Chai, Y. et al. Characterization of SNAP-25 gene from marine teleostean, Lateolabrax japonicus, ., Chin. J. Ocean. Limnol. 25, 378–385 (2007). https://doi.org/10.1007/s00343-007-0378-0
Characterization of SNAP-25 gene from marine teleostean, Lateolabrax japonicus[J]. 海洋湖沼学报(英文), 2007,25(4):378-385. DOI: 10.1007/s00343-007-0378-0.
Chen, K., Huang, X., Chai, Y. et al. Characterization of SNAP-25 gene from marine teleostean, Lateolabrax japonicus, ., Chin. J. Ocean. Limnol. 25, 378–385 (2007). https://doi.org/10.1007/s00343-007-0378-0 DOI:
The t-SNARE protein SNAP-25 (synaptosome-associated protein of 25 kDa) plays an essential role in regulating fusion between the vesicle and plasma membranes during exocytosis. To clone and characterize SNAP-25 gene
the first step in the functional study of SNARE proteins in marine teleostean
was to obtain the cDNA of sea perch SNAP-25 (SPsn25) by RT-PCR and RACE-PCR amplification of a Japanese sea perch. The full-length cDNA of 831bp contains a CDS of 615 bp
coding 204 amino acid residues
and a 5 UTR of 219bp. Bioinformatic analysis revealed that SPsn25 corresponds with SNAP-25a isoform and shares 91.1% identity with SNAP-25a of a goldfish and a zebrafish. The SPsn25 expression in both mRNA and protein levels in the Japanese sea perch had been identified through semi-quantitative RT-PCR and Western Blot assay. Together
these data again confirmed the nerve tissue specificity of the fish SNAP-25 gene expression.
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