Molecular cloning and functional characterization of HMGB1 and HMGB2 in large yellow croaker Larimichthys crocea

High mobility group box 1 (HMGB1) and HMGB2 have been demonstrated to be key regulators not only in DNA recombination, replication, gene transcription, but also in host inflammation and immune responses. In the present study, orthologs of HMGB1 and HMGB2 named Lc-HMGB1 and Lc-HMGB2 were characterized in large yellow croaker ( Larimichthys crocea ). The ORFs of Lc-HMGB1 and Lc-HMGB2 are 621 bp and 648 bp, encoding proteins of 206 aa and 215 aa, with the putative Lc- HMGB1 and Lc- HMGB2 proteins both contain two HMG domains, respectively. The genome organizations of Lc-HMGB1 and Lc-HMGB2 are both composed of four exons and three introns, which are conserved in vertebrates. Lc- HMGB1 and Lc- HMGB2 were identified as cell nucleus localized proteins, and were ubiquitously distributed in the examined organs/tissues. Additionally, Lc-HMGB1 was significantly up-regulated under LPS and PGN stimulation, whereas the stimulation of poly I:C, LPS, PGN, and Pseudomonas plecoglossicida infection could significantly induce Lc-HMGB2 expression in vivo . Notably, both Lc- HMGB1 and Lc- HMGB2 overexpression could significantly up-regulated the expression of diverse immune-related genes, including IFN1 , IRF3 , ISG15 , ISG56 , RSAD2 , g-type lysozyme , and TNF-α . Moreover, overexpression of Lc- HMGB1 could also induce the expression of IRF7 and Mx . These results collectively indicate that Lc -HMGB1 and Lc -HMGB2 play important roles in host immune responses against pathogen infection. • Lc -HMGB1 and Lc -HMGB2 were located in the cell nucleus. • Lc-HMGB1 can be induced by LPS and PGN stimulation. • Lc-HMGB2 can be induced by poly I:C, LPS, PGN, and Pseudomonas plecoglossicida stimulation. • Lc -HMGB1 and Lc -HMGB2 overexpression can induce antiviral, antibacterial, and inflammatory-related gene expression.