Zebrafish IRF1, IRF3, and IRF7 Differentially Regulate IFN Phi 1 and IFN Phi 3 Expression through Assembly of Homo- or Heteroprotein Complexes
Feng, Hui1,2; Zhang, Qi-Min1; Zhang, Yi-Bing1; Li, Zhi1; Zhang, Jun1; Xiong, Ya-Wei1; Wu, Min1; Gui, Jian-Fang1
刊名JOURNAL OF IMMUNOLOGY
2016-09-01
卷号197期号:5页码:1893-1904
ISSN号0022-1767
DOI10.4049/jimmunol.1600159
通讯作者Zhang, Yi-Bing(ybzhang@ihb.ac.cn)
英文摘要In mammals, IFN regulatory factor (IRF)1, IRF3, and IRF7 are three critical transcription factors that are pivotal for cooperative regulation of the type I IFN response. In this study, we explored the relative contribution of zebrafish (Danio rerio) IRF1 (DrIRF1), IRF3 (DrIRF3), and IRF7 (DrIRF7) (DrIRF1/3/7) to zebrafish IFN Phi 1 (DrIFN Phi 1) and IFN Phi 3 (DrIFN Phi 3) (DrIFN Phi 1/3) activation. Following spring viremia of carp virus infection, DrIFN Phi 1/3 and DrIRF1/3/7 transcripts are significantly induced in zebrafish tissues, which correlates with the replication of spring viremia of carp virus. DrIRF1/3/7 selectively bind to the IRF-binding element/IFN-stimulated regulatory element sites of DrIFN Phi 1/3 promoters, with the exception that DrIRF3 has no preference for two IRF-binding element/IFN-stimulated regulatory element motifs within the DrIFN Phi 3 promoter. Consistently, DrIRF3 alone activates DrIFN Phi 1, but not DrIFN Phi 3; DrIRF7 predominantly stimulates DrIFN Phi 3; and DrIRF1 has similar potential to DrIFN Phi 1 and DrIFN Phi 3. Strikingly, DrIRF3 facilitates the binding of DrIRF1 and DrIRF7 to both zebrafish IFN promoters, and so does DrIRF7 for the binding of DrIRF1, particularly to the DrIFN Phi 3 promoter. These binding properties correlate with differential responses of DrIFN Phi 1 and DrIFN Phi 3 to the combinatory stimulation of DrIRF1/3/7, depending on their relative amounts. Similar to the dual roles of human IRF3 in regulating IRF7-activated IFN alpha genes, DrIRF3 exerts dual effects on DrIRF1-mediated DrIFN Phi 3 gene expression: an inhibitory effect at lower concentrations and a synergistic effect at higher concentrations. These data provide evidence that fish and mammals have evolved a similar IRF-dependent regulatory mechanism fine-tuning IFN gene activation.
WOS关键词INTERFERON ANTIVIRAL RESPONSE ; CARP CARASSIUS-AURATUS ; I INTERFERON ; MOLECULAR CHARACTERIZATION ; TRANSCRIPTION FACTORS ; DENDRITIC CELLS ; SUBCELLULAR-LOCALIZATION ; AQUACULTURE ANIMALS ; FUNCTIONAL-ANALYSIS ; ATLANTIC SALMON
WOS研究方向Immunology
语种英语
出版者AMER ASSOC IMMUNOLOGISTS
WOS记录号WOS:000385002300037
内容类型期刊论文
源URL[http://ir.ihb.ac.cn/handle/342005/34143]  
专题水生生物研究所_鱼类生物学及渔业生物技术研究中心_期刊论文
通讯作者Zhang, Yi-Bing
作者单位1.Univ Chinese Acad Sci, Chinese Acad Sci, Inst Hydrobiol, State Key Lab Freshwater Ecol & Biotechnol, Wuhan 430072, Peoples R China
2.Univ North Carolina Chapel Hill, Lineberger Comprehens Canc Ctr, Chapel Hill, NC USA
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Feng, Hui,Zhang, Qi-Min,Zhang, Yi-Bing,et al. Zebrafish IRF1, IRF3, and IRF7 Differentially Regulate IFN Phi 1 and IFN Phi 3 Expression through Assembly of Homo- or Heteroprotein Complexes[J]. JOURNAL OF IMMUNOLOGY,2016,197(5):1893-1904.
APA Feng, Hui.,Zhang, Qi-Min.,Zhang, Yi-Bing.,Li, Zhi.,Zhang, Jun.,...&Gui, Jian-Fang.(2016).Zebrafish IRF1, IRF3, and IRF7 Differentially Regulate IFN Phi 1 and IFN Phi 3 Expression through Assembly of Homo- or Heteroprotein Complexes.JOURNAL OF IMMUNOLOGY,197(5),1893-1904.
MLA Feng, Hui,et al."Zebrafish IRF1, IRF3, and IRF7 Differentially Regulate IFN Phi 1 and IFN Phi 3 Expression through Assembly of Homo- or Heteroprotein Complexes".JOURNAL OF IMMUNOLOGY 197.5(2016):1893-1904.
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