Molecular cloning and functional characterization of interferon regulatory factor 7 of the barbel chub, Squaliobarbus curriculus
- PMID: 28842371
- DOI: 10.1016/j.fsi.2017.08.024
Molecular cloning and functional characterization of interferon regulatory factor 7 of the barbel chub, Squaliobarbus curriculus
Abstract
The interferon regulatory factor 7 (IRF7) is a critical regulator of type-I interferon-dependent immune reaction that defense against virus. To investigate the antiviral function of IRF7 of barbel chub Squaliobarbus curriculus (ScIRF7), the cDNA of ScIRF7 was cloned and characterized. The full length cDNA of ScIRF7 was 1870 bp, consisted of 41 bp 5'-UTR, 560 bp 3'-UTR and a 1269 bp open reading frame (ORF). The ORF encoded 423 amino acids with a molecular weight of 49.426 KDa and a theoretical isoelectric point of 5.71. The putative ScIRF7 protein possesses typical domains of IRF family including a conserved N-terminal DBD-binding domain (DBD), a C-terminal IRF association domain and a serine-rich domain. In the DBD, four tryptophans were found to be highly conserved among all species, whilst in another conserved tryptophan site of mammals, the corresponding amino acids were methionine for fishes. The expression level of ScIRF7 was highest in the spleen and lowest in the liver. The expression level of IFN-β was highest in the gill and lowest in the liver. After GCRV infection, expression levels changes of ScIRF7 showed an overall tendency of firstly up-regulation and then down-regulation in the spleen and the gill; and expression levels of ScIRF7 in peripheral blood lymphocyte at 24 h post-infection was highest among all time points. In pEGFP-ScIRF7 overexpressing cells, the mRNA level of ScIRF7 was firstly up-regulation and then down-regulation; and the expression of IFN-β was significantly up-regulated at 12 h post-infection than that of control group (P < 0.05), which was significantly higher than those in pEGFP-N1 overexpressing cells. The results indicated that ScIRF7 may play a key role in immune responses of barbel chub Squaliobarbus curriculus against GCRV and may also functions in the Ctenopharyngodon idellus kidney cells.
Keywords: Ctenopharyngodon idellus kidney cell; Grass carp reovirus; IFN-β; Interferon regulatory factor 7; Squaliobarbus curriculus.
Copyright © 2017. Published by Elsevier Ltd.
Similar articles
-
Involvement of interferon regulatory factor 3 from the barbel chub Squaliobarbus curriculus in the immune response against grass carp reovirus.Gene. 2018 Mar 30;648:5-11. doi: 10.1016/j.gene.2018.01.048. Epub 2018 Jan 12. Gene. 2018. PMID: 29339070
-
Sequence and expression analysis of the cytoplasmic pattern recognition receptor melanoma differentiation-associated gene 5 from the barbel chub Squaliobarbus curriculus.Fish Shellfish Immunol. 2019 Nov;94:485-496. doi: 10.1016/j.fsi.2019.08.077. Epub 2019 Sep 5. Fish Shellfish Immunol. 2019. PMID: 31494278
-
Tlr22 structure and expression characteristic of barbel chub, Squaliobarbus curriculus provides insights into antiviral immunity against infection with grass carp reovirus.Fish Shellfish Immunol. 2017 Jul;66:120-128. doi: 10.1016/j.fsi.2017.04.018. Epub 2017 Apr 22. Fish Shellfish Immunol. 2017. PMID: 28442418
-
Structural comparison and expression function analysis of BF/C2 in Ctenopharyngodon idella and Squaliobarbus curriculus.Fish Shellfish Immunol. 2023 Nov;142:109154. doi: 10.1016/j.fsi.2023.109154. Epub 2023 Oct 10. Fish Shellfish Immunol. 2023. PMID: 37821003 Review.
-
IRF7: role and regulation in immunity and autoimmunity.Front Immunol. 2023 Aug 10;14:1236923. doi: 10.3389/fimmu.2023.1236923. eCollection 2023. Front Immunol. 2023. PMID: 37638030 Free PMC article. Review.
Cited by
-
Transcriptional regulation and signaling of type IV interferon in Carassius gibelio.Cell Commun Signal. 2025 Jul 11;23(1):335. doi: 10.1186/s12964-025-02342-5. Cell Commun Signal. 2025. PMID: 40646525 Free PMC article.
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Research Materials