2014
DOI: 10.1016/j.dci.2014.07.019
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Molecular cloning and functional characterization of the NFIL3/E4BP4 transcription factor of grass carp, Ctenopharyngodon idella

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Cited by 20 publications
(6 citation statements)
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“…The factor that there was more expression of TRAF6 in survivors of breeding strain compared with those of non-breeding strain, is in line with the resistant related SNP on TRAF6 ( 62 ) and suggests the possible repression on the production of type I IFN ( 63 ). In addition, nuclear factor, interleukin 3 regulated (NFIL3) can control Treg cell function via directly binding to and negatively regulates the expression of Foxp3 ( 64 ), and has been revealed stimulating both proinflammatory (e.g., NF-kappa B [NF-κB]) and anti-inflammatory factors (e.g., IL10) in carp ( 65 ). Thus, the upregulated NFIL3 in the survivors of the breeding strain for group SvC-B may suggest the extensive activation of immune cells, with diminished immune regulation.…”
Section: Discussionmentioning
confidence: 99%
“…The factor that there was more expression of TRAF6 in survivors of breeding strain compared with those of non-breeding strain, is in line with the resistant related SNP on TRAF6 ( 62 ) and suggests the possible repression on the production of type I IFN ( 63 ). In addition, nuclear factor, interleukin 3 regulated (NFIL3) can control Treg cell function via directly binding to and negatively regulates the expression of Foxp3 ( 64 ), and has been revealed stimulating both proinflammatory (e.g., NF-kappa B [NF-κB]) and anti-inflammatory factors (e.g., IL10) in carp ( 65 ). Thus, the upregulated NFIL3 in the survivors of the breeding strain for group SvC-B may suggest the extensive activation of immune cells, with diminished immune regulation.…”
Section: Discussionmentioning
confidence: 99%
“…Primers were designed according to the RNA-Seq results, using Primer Premier 5 (Premier, Canada) ( S1 Table ) [ 43 ]. The arithmetic mean value of the 18S rRNA [ 44 46 ] and β -actin [ 47 49 ] genes of grass carp served as internal control value, to normalize the expression levels. After total RNA from each sample at each time point was extracted, reverse transcription was used to synthesize cDNA using the PrimeScript ™ RT reagent Kit with gDNA Eraser (Takara, Shanghai, China), according to the manufacturer’s instructions.…”
Section: Methodsmentioning
confidence: 99%
“…The ORF of Ctenopharyngodon idella tlr5 ( Citlr5 ) was amplified from grass carp cDNA and individually cloned into the pEGFP-N1 vector (Promega) by directional cloning. Invasion and proliferation assays were performed as previously described 17 . Using the Lipofectamin 2000 (Invitrogen) transfection reagent, 2 × 10 5 Ctenopharyngodon idella kidney (CIK) cells cellswere transfected with 1 μg pEGFP-N1-CiTLR5 plasmids or 50 nM cid-miRn-115 and miR-142a-3p agomir (GenePharm, China).…”
Section: Methodsmentioning
confidence: 99%