Title of article :
Molecular cloning, expression, and functional analysis of caspase-10 from Japanese flounder Paralichthys olivaceus
Author/Authors :
Kurobe، نويسنده , , Tomofumi and Hirono، نويسنده , , Ikuo and Kondo، نويسنده , , Hidehiro and Yamashita، نويسنده , , Michiaki and Aoki، نويسنده , , Takashi، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2007
Abstract :
We isolated and sequenced caspase-10 cDNA and gene from Japanese flounder, Paralichthys olivaceus. The Japanese flounder (JF)-caspase-10 cDNA consisted of 2282 bp and encoded 495 amino acid residues. The characteristic death effector domains (DEDs) of caspases were observed in JF-caspase-10 as well as the three aspartic acid residues (D-186, -382 and -392), which are potential cleavage sites for the large and small subunit structures. The amino acid residue (His-325) and pentapeptide (QACQG), which are involved in catalytic activity, were absolutely conserved in Japanese flounder-caspase-10. JF-caspase-10 gene has a length of 6.6 kb and consists of 11 exons and 10 introns similar to that of human. The strong expression of JF-caspase-10 mRNA was detected in the gills, peripheral blood leukocytes, spleen and posterior kidney, while the weak expression was observed in the head kidney, heart, intestine, skin and stomach. The over-expression analysis of JF-caspase-10 in Japanese flounder cell line HINAE was shown to induce apoptosis 24 h post-transfection using TUNEL assay.
Keywords :
Caspase-10 , gene cloning , RT-PCR , Over-expression analysis , TUNEL assay , Japanese flounder (Paralichthys olivaceus)
Journal title :
Fish and Shellfish Immunology
Journal title :
Fish and Shellfish Immunology