2010
DOI: 10.1128/jvi.02291-09
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A Novel Inhibitor of the NF-κB Signaling Pathway Encoded by the Parapoxvirus Orf Virus

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Cited by 59 publications
(104 citation statements)
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“…Thus ORFV024 protein from the parapoxvirus orf virus was shown to block IKK activation although the mechanism of its activity is not clear [34], while two other unique parapoxvirus proteins, ORFV002 and ORFV121, were recently shown to also inhibit NFkB activation. ORFV002 antagonized p65 phosphorylation by interfering with the association of p65 with the mitogen and stress-activated kinase-1 (MSK1) which prevented p65 recruiting the coactivator p300 to NFkB-dependent promoters, thus suppressing transactivation [35].…”
Section: Direct Targeting Of Nfkb and Its Proximal Kinases By Poxvirusesmentioning
confidence: 99%
“…Thus ORFV024 protein from the parapoxvirus orf virus was shown to block IKK activation although the mechanism of its activity is not clear [34], while two other unique parapoxvirus proteins, ORFV002 and ORFV121, were recently shown to also inhibit NFkB activation. ORFV002 antagonized p65 phosphorylation by interfering with the association of p65 with the mitogen and stress-activated kinase-1 (MSK1) which prevented p65 recruiting the coactivator p300 to NFkB-dependent promoters, thus suppressing transactivation [35].…”
Section: Direct Targeting Of Nfkb and Its Proximal Kinases By Poxvirusesmentioning
confidence: 99%
“…HeLa cells stably expressing green fluorescent protein (GFP) (GFP/HeLa) or ORFV121-GFP (121GFP/ HeLa) fusion protein were established as previously described (11) and maintained in Dulbecco's modified essential medium (DMEM) supplemented with 10% FBS, 2 mM L-glutamine, gentamicin (50 g/ml), penicillin (100 g/ml), streptomycin (100 g/ml), and neomycin (G418; 500 g/ml; Gibco). ORFV strain OV-IA82 (10) was used to construct an ORFV121 deletion mutant virus (OV-IA82⌬121) in all procedures involving wild-type virus infection and in the cloning of viral genes.…”
Section: Cells and Virusesmentioning
confidence: 99%
“…Cells were inoculated with OV-IA82 (multiplicity of infection [MOI], 10) in the presence or absence of cytosine arabinoside (AraC; 40 g/ml) and harvested at 0, 1, 2, 3, 6, 12, and 24 h postinoculation (p.i.). RNA samples were processed and reverse transcribed as previously described (11). The transcription of ORFV121, ORFV024 (early control gene), and ORFV059 (late control gene) was assessed by PCR using primers 121Fw (5Ј-TCCAGCTGCCCGCGACGACGCGC-3Ј), 121Rv (5Ј-GGAGGTTGGGTCTGCCGGCGCCGCA-3Ј), 024Fw (5Ј-GCGGA CACAGCCACAACCACAGTC-3Ј), 024Rv (5Ј-CTAGCACGCGCTTTCGGT ACCGCC-3Ј), 059Fw (5Ј-ATGGATCCACCCGAAATCAC-3Ј), and 059Rv (5Ј-TCACACGATGGCCGTGACCAGC-3Ј), respectively.…”
Section: Cells and Virusesmentioning
confidence: 99%
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