Cloning and expression of a transcription factor activator protein-1 member identified from the swimming crab Portunus trituberculatus
Cell Stress and Chaperones, ISSN: 1355-8145, Vol: 23, Issue: 6, Page: 1275-1282
2018
- 5Citations
- 2Captures
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Metrics Details
- Citations5
- Citation Indexes5
- CrossRef4
- Captures2
- Readers2
Article Description
Transcription activator proteins are regulatory proteins that bind to the promoter regions of target genes. Transcription activator protein-1 (AP-1) regulates numerous genes related to the immune system, apoptosis, and proliferation. In this study, the full-length cDNA of AP-1 from Portunus trituberculatus ( PtAP-1 ) was identified by expressed sequence tag analysis and cDNA-end rapid amplification. The gene is 1183 bp and encodes a 256-amino acid protein with a predicted molecular mass and isoelectric point of 28.96 kDa and 8.90, respectively. PtAP-1 showed the highest expression level in the gonad tissue and the lowest expression level in blood, hemocyte, muscle, hepatopancreas, and gill, during the first 6 h of low-salinity stimulation (10%). Additionally, we observed steady decreases in PtAP-1 mRNA expression in the gill, but at 12 h, expression was initially upregulated, followed by a significant decrease until restoration to baseline levels at 48 h. Additionally, Vibrio alginolyticus challenge resulted in significant upregulation of PtAP-1 expression in the first 6 h, which was maintained at high levels for 48 h. From 48 to 72 h, we observed decreases in PtAP-1 levels, although they remained significantly higher than those detected at baseline. These results suggested that PtAP-1 is involved in the immune response and osmoregulation of crustaceans.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S1355814523008192; http://dx.doi.org/10.1007/s12192-018-0935-9; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85053908664&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/30255490; https://linkinghub.elsevier.com/retrieve/pii/S1355814523008192; https://dx.doi.org/10.1007/s12192-018-0935-9
Elsevier BV
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