您好,欢迎访问中国水产科学研究院 机构知识库!

Gene cloning and expression analysis of IRF1 in half-smooth tongue sole (Cynoglossus semilaevis)

文献类型: 外文期刊

作者: Lu, Yang 1 ; Wang, Qilong 1 ; Liu, Yang 3 ; Shao, Changwei 1 ; Chen, Songlin 1 ; Sha, Zhenxia 1 ;

作者机构: 1.Chinese Acad Fisheries Sci, Yellow Sea Fisheries Res Inst, Minist Agr, Key Lab Sustainable Utilizat Marine Fisheries Res, Qingdao 266071, Peoples R China

2.Shanghai Ocean Univ, Coll Fisheries & Life Sci, Shanghai 201306, Peoples R China

3.Dalian Ocean Univ, Key Lab North Mariculture & Stock Enhancement Nor, Minist Agr, Dalian 116023, Peoples R China

关键词: IRF1;Cynoglossus semilaevis;Expression;Vibrio anguillarum;Lymphocystis disease virus (LCDV)

期刊名称:MOLECULAR BIOLOGY REPORTS ( 影响因子:2.316; 五年影响因子:2.357 )

ISSN:

年卷期:

页码:

收录情况: SCI

摘要: Interferon regulatory factor 1 (IRF1) was known to play key roles in antiviral defense in several species, and some other important biological processes. In this report, full length cDNA of IRF1 from Cynoglossus semilaevis (CsIRF1) was identified. It was of 1,455 bp, containing a 5' UTR of 104 bp, a 3' UTR of 541 bp with a poly (A) tail and an ORF of 810 bp encoding a putative protein of 269 amino acids. The putative CsIRF1protein contained one conserved IRF domain (1-113aa), and two low complexity regions (140-158aa and 230-242aa, respectively). Phylogenetic analysis showed that CsIRF1 was conserved in the teleost evolutionary branch, which was independent of mammalian, birds and amphibians. Additionally, CsIRF1 had the 96 % homology with marine fishes, while 66 % with freshwater fishes. The expression profiles of CsIRF1was analyzed by quantitative real-time PCR in healthy tissues and in immune tissues challenged with different pathogens [Vibrio anguillarum and Lymphocystis disease virus (LCDV)], respectively. CsIRF1 was widely expressed in healthy tissues of Cynoglossus semilaevis and with the highest expression in blood, as much as 19 times of that in liver. V. anguillarum and LCDV both induced the CsIRF1 gene expression distinctly in liver, with the peak value reached to 98-fold at 6 h and 25-fold at 24 h, respectively. The bacteria induced CsIRF1 suddenly up-expression in each detected tissues. However, at the initial stage of the challenge of virus LCDV, the CsIRF1 expression in blood and spleen were up regulated; on the contrary, its expression in liver and head kidney were down regulated, 0.3 and 0.4-fold 6 h post virus injection, respectively. These results suggested that CsIRF1 gene might involve in not only antiviral activity but also antibacterial procedure, indicating its vital role in Cynoglossus semilaevis innate defense system.

  • 相关文献

[1]MHC polymorphism and disease resistance to vibrio anguillarum in 8 families of half-smooth tongue sole (Cynoglossus semilaevis). Du, Min,Chen, Song-lin,Liu, Yang,Yang, Jing-feng,Du, Min,Du, Min,Liu, Yan-hong. 2011

[2]Transcriptome analysis revealed changes of multiple genes involved in immunity in Cynoglossus semilaevis during Vibrio anguillarum infection. Zhang, Xiang,Chen, Songlin,Chen, Yadong,Shao, Changwei,Wang, Qilong,Lu, Yang,Gong, Guangye,Sha, Zhenxia,Zhang, Xiang,Ding, Shaoxiong,Wang, Shaolin,Liu, Yang.

[3]Identification and characterization of Cynoglossus semilaevis microRNA response to Vibrio anguillarum infection through high-throughput sequencing. Sha, Zhenxia,Gong, Guangye,Lu, Yang,Wang, Lei,Chen, Songlin,Gong, Guangye,Lu, Yang,Wang, Shaolin,Wang, Qilong.

[4]Expression Profiling Analysis of the microRNA Response of Cynoglossus semilaevis to Vibrio anguillarum and Other Stimuli. Gong, Guangye,Sha, Zhenxia,Chen, Songlin,Yan, Hui,Chen, Yadong,Wang, Tianzi,Li, Chao,Yan, Hui.

[5]Expression Profile Analysis of miR-221 and miR-222 in Different Tissues and Head Kidney Cells of Cynoglossus semilaevis, Following Pathogen Infection. Yan, Hui,Chen, Yadong,Gong, Guangye,Chen, Xuejie,Wang, Tianzi,Chen, Songlin,Sha, Zhenxia,Chen, Yadong,Chen, Songlin,Sha, Zhenxia,Zhou, Shun,Li, Chao.

[6]Molecular cloning and expression analysis of Relish gene from the ridgetail white prawn Exopalaemon carinicauda. Ge, Qianqian,Ge, Qianqian,Li, Jitao,Li, Jian,Zhao, Fazhen,Ren, Hai,Liang, Junping,Duan, Yafei.

[7]cDNA cloning, tissues, embryos and larvae expression analysis of Sox10 in half-smooth tongue-sole, Cynoglossus semilaevis. Deng, Si-Ping,Chen, Song-Lin,Deng, Si-Ping,Chen, Song-Lin,Deng, Si-Ping.

[8]MHC polymorphism and disease resistance to Vibrio anguillarum in 12 selective Japanese flounder (Paralichthys olivaceus) families. Xu, Tian-jun,Chen, Song-lin,Ji, Xiang-shan,Tian, Yong-sheng,Xu, Tian-jun. 2008

[9]MHC class II alpha gene polymorphism and its association with resistance/susceptibility to Vibrio anguillarum in Japanese flounder (Paralichthys olivaceus). Xu, Tian-jun,Chen, Song-lin,Zhang, Yu-xi,Xu, Tian-jun. 2010

[10]Cloning, characterization, and expression of a novel member of proteasomal subunits gene in turbot, Scophthalmus maximus. Zhang Bo,Song Wenping,Zheng Debin,Ma Chao,Xiao Guangxia,Wang Xianli. 2015

[11]Effects of dietary supplementation of A3 alpha-peptidoglycan on innate immune responses and defense activity of Japanese flounder (Paralichthys olivaceus). Zhou, J,Song, XL,Huang, J,Wang, XH. 2006

[12]Molecular responses of calreticulin gene to Vibrio anguillarum and WSSV challenge in the ridgetail white prawn Exopalaemon carinicauda. Duan, Yafei,Liu, Ping,Li, Jitao,Li, Jian,Chen, Ping,Duan, Yafei,Wang, Yun. 2014

[13]Ability of Lactobacillus plantarum lipoteichoic acid to inhibit Vibrio anguillarum-induced inflammation and apoptosis in silvery pomfret (Pampus argenteus) intestinal epithelial cells. Gao, Quanxin,Min, Minghua,Zhang, Chenjie,Peng, Shiming,Shi, Zhaohong,Gao, Qian.

[14]A Genome Scan for Quantitative Trait Loci Associated with Vibrio anguillarum Infection Resistance in Japanese Flounder (Paralichthys olivaceus) by Bulked Segregant Analysis. Wang, Lei,Wang, Lei,Fan, Caixia,Liu, Yang,Zhang, Yingping,Deng, Han,Xu, Ying,Tian, Yongsheng,Liao, Xiaolin,Xie, Mingshu,Li, Wenlong,Chen, Songlin,Wang, Lei,Liu, Shoutang,Sun, Deqiang.

[15]Identification and expression analysis of fetuin B (FETUB) in turbot (Scophthalmus maximus L.) mucosal barriers following bacterial challenge. Li, Chao,Gao, Chengbin,Fu, Qiang,Chen, Jinghua,Su, Baofeng,Su, Baofeng.

[16]The responsive expression of a chitinase gene in the ridgetail white prawn Exopalaemon carinicauda against Vibrio anguillarum and WSSV challenge. Duan, Yafei,Liu, Ping,Li, Jitao,Li, Jian,Chen, Ping,Duan, Yafei,Wang, Yun.

[17]RNA-Seq analysis of immune-relevant genes in Lateolabrax japonicus during Vibrio anguillarum infection. Zhao, Chao,Fu, Mingjun,Wang, Chengyang,Qiu, Lihua,Wang, Chengyang,Zhao, Chao,Fu, Mingjun,Wang, Chengyang,Qiu, Lihua,Qiu, Lihua,Jiao, Zongyao.

[18]Molecular characterization and immune response expression of the QM gene from the scallop Chlamys farreri. Chen, Guofu,Zhang, Chunyun,Wang, Yue,Wang, Yuanyuan,Guo, Changlu,Wang, Chongming.

[19]The involvement of cathepsin F gene (CTSF) in turbot (Scophthalmus maximus L.) mucosal immunity. Gao, Chengbin,Fu, Qiang,Song, Huanhuan,Zhou, Shun,Li, Chao,Tan, Fenghua,Su, Baofeng,Su, Baofeng,Fu, Qiang.

[20]Identification, characterization and expression analysis of TLR5 in the mucosal tissues of turbot (Scophthalmus maximus L.) following bacterial challenge. Liu, Fengqiao,Fu, Qiang,Gao, Chengbin,Li, Chao,Su, Baofeng,Shang, Mei,Su, Baofeng,Shang, Mei,Tan, Fenghua.

作者其他论文 更多>>