Expression characterization, genomic structure and function analysis of fish ubiquitin-specific protease 18 (USP18) genes

被引:12
|
作者
Chen, Chen [1 ]
Zhang, Yi-Bing [1 ]
Gui, Jian-Fang [1 ]
机构
[1] Univ Chinese Acad Sci, Chinese Acad Sci, Inst Hydrobiol, State Key Lab Freshwater Ecol & Biotechnol, Wuhan 430072, Peoples R China
来源
DEVELOPMENTAL AND COMPARATIVE IMMUNOLOGY | 2015年 / 52卷 / 02期
基金
中国国家自然科学基金;
关键词
Ubiquitin-specific protease 18; Interferon-stimulated gene; Expression regulation; Subcellular localization; Promoter analysis; ANTIVIRAL RESPONSE; IMMUNE-RESPONSE; INTERFERON; ISG15; UBP43; ZEBRAFISH; SYSTEM; CELLS; STAT1; GASTRULATION;
D O I
10.1016/j.dci.2015.05.003
中图分类号
S9 [水产、渔业];
学科分类号
0908 ;
摘要
In mammals, USP18 (ubiquitin-specific protease 18) is an interferon (IFN) inducible protein and plays a role in regulation of IFN response upon viral infection. In this study, we first cloned a USP18 homologous gene from virally-infected crucian carp (Carassius auratus) blastula embryonic (CAB) cells, and later found in other fish species including zebrafish. All fish USP18 genes have 10 exons and 9 introns comparable toll exons and 10 introns in non-fish vertebrates. Expression analysis revealed that fish USP18 was significantly induced in vitro and in vivo by IFN and IFN stimuli. Using promoter-driven luciferase reporter assay system to explore the molecular mechanism underlying fish USP18 expression, fish USP18 was identified as a typical interferon (IFN)-stimulated gene (ISG). Intracellular poly(I:C)-triggered zebrafish USP18 expression was regulated through RLR-IFN pathway, which was consistent with the fact that fish USP18 gene promoter contained two typical IFN-stimulated response elements (ISREs). Further mutation assays revealed that the distant ISRE motif primarily contributed to the induction of zebrafish USPI8 by fish IFN and IFN stimuli. Functionally, fish USP18 inhibited poly(I:C)- and IFN-triggered activation of a common ISRE-containing promoter, and attenuated transcriptional expression of some ISGs including Stat1 and PKZ by recombinant IFN. Finally, we found that fish USP18 protein was expressed in cytoplasm and exhibited an ability to interact with ISG15. These results indicate that fish USPI8 likely exerts its function similar to mammalian homologs. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:112 / 122
页数:11
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