Molecular cloning and multifunctional characterization of GRIM-19 (gene associated with retinoid-interferon-induced mortality 19) homologue from turbot (Scophthalmus maximus)

被引:6
作者
Wang, Na [1 ]
Wang, Xianli [2 ]
Yang, Changgeng [3 ]
Zhao, Xiaojie [4 ]
Zhang, Yuxi [5 ]
Wang, Tianzi [1 ]
Chen, Songlin [1 ]
机构
[1] Chinese Acad Fishery Sci, Yellow Sea Fisheries Res Inst, Qingdao 266071, Peoples R China
[2] Tongji Univ, Sch Med, Sarite Ctr Stem Cell Engn Translat Med, East Hosp,Stem Cell Res Ctr, Shanghai 200120, Peoples R China
[3] Chinese Acad Fishery Sci, Yangtze River Fisheries Res Inst, Key Lab Freshwater Biodivers Conservat & Utilizat, Minist Agr, Wuhan 430223, Peoples R China
[4] State Ocean Adm, Weifang Marine Environm Monitoring Cent Stn, Weifang 261041, Peoples R China
[5] Qingdao Agr Univ, Qingdao 266109, Peoples R China
基金
中国国家自然科学基金; 国家高技术研究发展计划(863计划);
关键词
GRIM-19; Turbot (Scophthalmus maximus); Immune response; Cell apoptosis; STAT3; NF-kappa B; DEATH REGULATOR GRIM-19; CELL-DEATH; PROTEIN; ACID; IDENTIFICATION; CANCER; COMBINATION; EXPRESSION; INTERACTS; PRODUCT;
D O I
10.1016/j.dci.2013.11.004
中图分类号
S9 [水产、渔业];
学科分类号
0908 ;
摘要
GRIM-19 (gene associated with retinoid-interferon-induced mortality 19), a novel cell death regulatory gene, plays important roles in cell apoptosis, embryogenesis, mitochondrial respiratory chain and immune response. To date, little information is known about fish GRIM-19 characteristics except orange-spotted grouper (Epinephelus coioides). Here a new GRIM-19 gene is identified and characterized from turbot (Scophthalmus maximus), an economic marine fish in China and Europe. Briefly, turbot GRIM-19 is a 595-bp gene encoding a 144 amino acids protein, which shares the closest relationship with Atlantic halibut (Hippoglossus hippoglossus). The expression of turbot grim-19 in liver, spleen and kidney is up-regulated by the infection of Vibrio anguillarum and LCDV (lymphocystis disease virus). Subsequently, a recombinant protein of turbot GRIM-19 is acquired and the anti-bacterial function is proved by liquid culture inhibition experiment. The subcellular location indicates that turbot GRIM-19 is co-localized with STAT3 in the cytoplasm, which is mainly determined by GRIM-19 41-84 amino acids and STAT3 1-321 amino acids. Finally, the involvements of turbot GRIM-19 in cell apoptosis and NF-kappa B pathway are investigated. All these data help to understand GRIM-19 function in fish, as well as provide the application possibility of GRIM-19 in fish disease resistance breeding. (C) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:96 / 105
页数:10
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