Transcriptional regulation of type I interferon gene expression by interferon regulatory factor-3 in Japanese flounder, Paralichthys olivaceus
► Japanese flounder type I IFN gene was cloned and clustered with Acanthopterygii. ► The poly I:C-responsible region (−634 to −179bp) was found in IFN promoter. ► Transcriptional activity of IFN promoter was enhanced by the flounder IRF3. ► The activity of IFN promoter was induced by RLRs after poly...
Gespeichert in:
Veröffentlicht in: | Developmental and comparative immunology 2012-04, Vol.36 (4), p.697-706 |
---|---|
Hauptverfasser: | , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | ► Japanese flounder type I IFN gene was cloned and clustered with Acanthopterygii. ► The poly I:C-responsible region (−634 to −179bp) was found in IFN promoter. ► Transcriptional activity of IFN promoter was enhanced by the flounder IRF3. ► The activity of IFN promoter was induced by RLRs after poly I:C-stimulation.
Type I interferon (IFN) induces the antiviral response in innate immunity. The type I IFN gene cloned from Japanese flounder (Paralichthys olivaceus) has a length of 1189bp and consisting of 5 exons and 4 introns. In a phylogenetic tree of type I IFNs, Japanese flounder grouped with other Acanthopterygii. To gain insight into the transcriptional regulation of IFN gene, the 1.36kb 5′-upstream region including numerous canonical motifs to bind transcription factors [for example, IFN regulatory factor (IRF)] was analyzed. In HINAE cells using a luciferase reporter assay, poly I:C-responsive transcriptional activity was found in the region from −634 to −179bp. This region includes several IRF motifs. In the presence of poly I:C, overexpression of IRF3 and RLR strongly enhanced transcriptional activity. These results suggest that the transcriptional regulation of Japanese flounder type I IFN is regulated by IRF3 after triggering with dsRNA sensors. |
---|---|
ISSN: | 0145-305X 1879-0089 |
DOI: | 10.1016/j.dci.2011.10.008 |