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• W2437043699 abstract "Rift Valley fever (RVF) is a zoonotic disease that can cause severe illness in humans and livestock, triggering spontaneous abortion in almost 100% of pregnant ruminants. In this study, we demonstrate that signal transducer and activator of transcription 3 (STAT3) is phosphorylated on its conserved tyrosine residue (Y705) following RVFV infection. This phosphorylation was dependent on a major virulence factor, the viral nonstructural protein NSs. Loss of STAT3 had little effect on viral replication, but rather resulted in cells being more susceptible to RVFV-induced cell death. Phosphorylated STAT3 translocated to the nucleus, coinciding with inhibition of fos, jun, and nr4a2 gene expression, and the presence of STAT3 and NSs at the nr4a2 promoter. NSs was found predominantly in the cytoplasm of STAT3 null cells, indicating that STAT3 influences NSs nuclear localization. Collectively, these data demonstrate that STAT3 functions in a pro-survival capacity through modulation of NSs localization." @default.
• W2437043699 created "2016-06-24" @default.
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• W2437043699 date "2016-09-01" @default.
• W2437043699 modified "2023-10-06" @default.
• W2437043699 title "The role of signal transducer and activator of transcription 3 in Rift Valley fever virus infection" @default.
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• W2437043699 doi "https://doi.org/10.1016/j.virol.2016.06.004" @default.
• W2437043699 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/4969177" @default.
• W2437043699 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/27318793" @default.
• W2437043699 hasPublicationYear "2016" @default.
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