1. Identification and characterization of a carboxypeptidase N1 from red lip mullet (Liza haematocheila); revealing its immune relevance.
- Author
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Perera NCN, Godahewa GI, Jung S, Kim MJ, Nam BH, and Lee J
- Subjects
- Amino Acid Sequence, Animals, Base Sequence, Carboxypeptidases chemistry, Fish Proteins chemistry, Fish Proteins genetics, Fish Proteins immunology, Gene Expression Profiling veterinary, Gram-Positive Bacterial Infections immunology, Lactococcus physiology, Phylogeny, Poly I-C pharmacology, Sequence Alignment veterinary, Carboxypeptidases genetics, Carboxypeptidases immunology, Fish Diseases immunology, Gene Expression Regulation immunology, Immunity, Innate genetics, Smegmamorpha genetics, Smegmamorpha immunology
- Abstract
Complement system orchestrates the innate and adaptive immunity via the activation, recruitment, and regulation of immune molecules to destroy pathogens. However, regulation of the complement is essential to avoid injuries to the autologous tissues. The present study unveils the characteristic features of an important complement component, anaphylatoxin inactivator from red lip mullet at its molecular and functional level. Mullet carboxypeptidase N1 (MuCPN1) cDNA sequence possessed an open reading frame of 1347 bp, which encoded a protein of 449 amino acids with a predicted molecular weight of 51 kDa. In silico analysis discovered two domains of PM14-Zn carboxypeptidase and a C-terminal domain of M14 N/E carboxypeptidase, two zinc-binding signature motifs, and an N-glycosylation site in the MuCPN1 sequence. Homology analysis revealed that most of the residues in the sequence are conserved among the other selected homologs. Phylogeny analysis showed that MuCPN1 closely cladded with the Maylandia zebra CPN1 and clustered together with the teleostean counterparts. A challenge experiment showed modulated expression of MuCPN1 upon polyinosinic:polycytidylic acid and Lactococcus garviae in head kidney, spleen, gill, and liver tissues. The highest upregulation of MuCPN1 was observed 24 h post infection against poly I:C in each tissue. Moreover, the highest relative expressions upon L. garviae challenge were observed at 24 h post infection in head kidney tissue and 48 h post infection in spleen, gill, and liver tissues. MuCPN1 transfected cells triggered a 2.2-fold increase of nitric oxide (NO) production upon LPS stimulation compared to the un-transfected controls suggesting that MuCPN1 is an active protease which releases arginine from complement C3a, C4a, and C5a. These results have driven certain way towards enhancing the understanding of immune role of MuCPN1 in the complement defense mechanism of red lip mullet., (Copyright © 2018 Elsevier Ltd. All rights reserved.)
- Published
- 2019
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