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• W2616831711 endingPage "893" @default.
• W2616831711 startingPage "889" @default.
• W2616831711 abstract "The transcription factors Oct-1 and Oct-2 bind differentially to three octamer binding sequences corresponding to the octamer binding site from the H2B promoter [ATGCTAATAA], a simple TAATGARAT motif, found in herpes simplex virus IE4/5 genes [GCGGTAATGAGAT], and a perfect consensus overlapping octamer/TAATGARAT motif [ATGCTAATGAGAT]. By comparing the effects of protein kinase A, protein kinase C and casein kinase 2 in vitro on the binding of Oct-1 and Oct-2 to the three motifs, we show that the actions of these kinases regulate Oct-1 and Oct-2 DNA binding independently of each other in a binding-site-specific manner. Inhibition of cellular phosphatases also regulate Oct-1 and Oct-2 DNA binding in a binding-site-specific manner. Both kinase and phosphatase activity are important for regulating the DNA binding activity of Oct-1 and Oct-2 because, in the presence of phosphatase inhibitors, protein kinase A attenuates the binding of both Oct-1 and Oct-2 to the octamer binding site but enhances binding when phosphatase inhibitors are omitted. Thus the DNA specificity of Oct-1 and Oct-2 can be regulated in vitro by the action of different kinases." @default.
• W2616831711 created "2017-05-26" @default.
• W2616831711 creator A5002956062 @default.
• W2616831711 creator A5018944500 @default.
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• W2616831711 date "1996-05-01" @default.
• W2616831711 modified "2023-09-28" @default.
• W2616831711 title "Oct-1 [corrected] and Oct-2 DNA-binding site specificity is regulated in vitro by different kinases" @default.
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• W2616831711 doi "https://doi.org/10.1042/bj3150889" @default.
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• W2616831711 hasPublicationYear "1996" @default.
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