Title of article :
Characterization of the BPI-like gene from a subtracted cDNA library of large yellow croaker (Pseudosciaena crocea) and induced expression by formalin-inactivated Vibrio alginolyticus and Nocardia seriolae vaccine challenges
Author/Authors :
Huang، نويسنده , , Yanqing and Lou، نويسنده , , Huifang and Wu، نويسنده , , Xinzhong and Chen، نويسنده , , Yanxia، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2008
Pages :
11
From page :
740
To page :
750
Abstract :
One expressed sequence tag (EST 64LF004 clone), which is from the subtracted cDNA library of the head kidney of large yellow croaker (Pseudosciaena crocea) stimulated with peptidoglycan (PG) by suppression subtractive hybridization (SSH) method, was cloned using RACE–PCR. The full length cDNA, which possesses typical structural features of a signal peptide, a conserved LPS binding domain and two bactericidal permeability-increasing (BPI) motifs as in higher vertebrates, was identified as a novel homologue, namely of the large yellow croaker BPI-like molecule (Pc-BPI-L). Phylogenetic analysis showed this Pc-BPI-L of large yellow croaker as the most ancestral branch in bony fish clade. The recombinant Pc-BPI-L protein expressed in the Tn-5B1-4 insect cells was successfully produced and confirmed to have the predicted size of 52 kDa by Western blot analysis. At the message level, Pc-BPI-L mRNA was ubiquitously expressed in all tissues examined. Following formalin-inactivated Vibrio alginolyticus and Nocardia seriolae treatment, Pc-BPI-L message was differentially up-regulated in primary immune organs. These results indicate that Pc-BPI-L might be involved in the immune response to bacterial infection.
Keywords :
Suppression subtraction hybridization , Lipopolysaccharide , Bactericidal permeability-increasing protein , Pc-BPI-like gene , Eukaryotic Expression , Large yellow croaker (Pseudosciaena crocea)
Journal title :
Fish and Shellfish Immunology
Serial Year :
2008
Journal title :
Fish and Shellfish Immunology
Record number :
2108294
Link To Document :
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