Molecular characterization, tissue distribution and functional analysis of galectin 1-like 2 in grass carp (Ctenopharyngodon idella)

被引:11
作者
Zhu, Denghui [1 ,2 ]
Fu, Peipei [1 ,2 ,4 ]
Huang, Rong [1 ]
Xiong, Lv [1 ,2 ]
Wang, Yumeng [5 ]
He, Libo [1 ]
Liao, Lanjie [1 ]
Li, Yongming [1 ]
Zhu, Zuoyan [1 ]
Wang, Yaping [1 ,3 ]
机构
[1] Chinese Acad Sci, Inst Hydrobiol, State Key Lab Freshwater Ecol & Biotechnol, Wuhan 430072, Hubei, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
[3] Chinese Acad Sci, Innovat Acad Seed Design, Beijing 100101, Peoples R China
[4] Chinese Acad Sci, Inst Hydrobiol, Minist Agr, Key Lab Aquaculture Dis Control, Wuhan 430072, Hubei, Peoples R China
[5] Wuhan Univ, Wuhan 430072, Hubei, Peoples R China
基金
中国国家自然科学基金;
关键词
Galectin-1; Innate immunity; Grass carp reovirus; Microbial ligand binding; Subcellular localization; ZEBRAFISH DANIO-RERIO; TELEOST FISH; GENE FAMILY; EXPRESSION; INNATE; VIRUS; RECEPTORS; DIVERSITY; SECRETION; LECTINS;
D O I
10.1016/j.fsi.2019.09.041
中图分类号
S9 [水产、渔业];
学科分类号
0908 ;
摘要
Galectins, as an evolutionary conserved group of lectin superfamily, has the functions of pathogen recognition, anti-bacteria and anti-virus. In this study, a 405 bp cDNA sequence of galectin 1-like 2 (CiGal1-L2) was obtained from grass carp (Ctenopharyngodon idella), which encoded 134 amino acids with a predicted molecular mass of 15.143 kDa and an isoelectric point of 5.33. The sugar binding motifs (H-N-R, V-N and W-E-R) were detected in carbohydrate-binding domain (CRD). The amino acid sequence similarity showed that CiGall-L2 was 40.30-42.54% and 66.42-81.20% similarity to mammalian and fish counterparts, respectively. The phylogenetic tree showed that CiGal1-L2 was clustered with fish galectin-is and closely related to Cyprinus carpio. Real-time quantitative PCR (RT-qPCR) analysis revealed that CiGal1-L2 was widely expressed in all tested tissues. In addition, the expression of CiGal1-L2 was differentially up-regulated challenged with grass carp reovirus (GCRV), lipopolysaccharide (LPS) and polyinosinic:polycytidylic acid (poly I:C). The fluorescence of CiGal1-L2-GFP was distributed in the cytoplasm and nucleus of HEK 293T cells and showed a trend of nuclear translocation after LPS and poly I:C treatment. Finally, the recombinant CiGal1-L2 (rCiGal1-L2) protein showed strong binding ability to LPS. In conclusion, the results provided further insight into the immune roles of galectin-1 in teleost.
引用
收藏
页码:455 / 463
页数:9
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