Abstract
By computer search, we identified one potential NF-κB binding site in the HPV16 long control region (LCR) at position 7554-7563 having two mismatches in comparison to the consensus NF-κB binding site of the lg(K) L promoter. Bandshift experiments with nuclear extracts from HeLa cells or purified glutathione S-transferase-p65 fusion protein clearly demonstrated that NF-κB is able to bind to this region of the LCR. However, in comparison to NF-κB binding on a consensus probe, the affinity of NF-κB for this site is about 250-fold reduced. When mutations were introduced into this NF-κB binding site, the activity of the LCR was increased, strongly suggesting that NF-κB was acting as a transcriptional repressor in the context of the HPV16 LCR. In addition, overexpression of NF-κB p65 repressed the activity of the HPV16 LCR, strengthening this conclusion. (C) 2000 Academic Press.
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CITATION STYLE
Fontaine, V., Van Der Meijden, E., De Graaf, J., Ter Schegget, J., & Struyk, L. (2000). A functional NF-κB binding site in the human papillomavirus type 16 long control region. Virology, 272(1), 40–49. https://doi.org/10.1006/viro.2000.0363
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