Journal
JOURNAL OF VIROLOGY
Volume 75, Issue 9, Pages 4283-4296Publisher
AMER SOC MICROBIOLOGY
DOI: 10.1128/JVI.75.9.4283-4296.2001
Keywords
-
Categories
Ask authors/readers for more resources
Infection with high-risk human papillomaviruses (HPV) is a major risk factor for development of cervical cancer. Expression of the HPV E6 and E7 oncoproteins increases in differentiating keratinocytes, resulting in inactivation of the p53 and retinoblastoma proteins, two important transcriptional regulators. We used cDNA microarrays to examine global alterations in gene expression in differentiating cervical keratinocytes after infection with retroviruses encoding HPV type 16 (HPV-16) E6 and E7, Expression of 80 cellular genes (approximately 4% of the genes on the array) was altered reproducibly by E6 and/or E7, Cluster analysis classified these genes into three Functional groups: (i) interferon (IFN)-responsive genes, (ii) genes stimulated by NF-kappaB, and (iii) genes regulated in cell cycle progression and DNA synthesis. HPV-16 E6 or a dominant negative p53 protein downregulated multiple IFN-responsive genes. E6 decreased expression of IFN-alpha and -beta, downregulated nuclear STAT-I protein, and decreased binding of STAT-I to the IFN-stimulated response element. E7 alone was less effective; however, coexpression of E6 and E7 downregulated IFN-responsive genes more efficiently than E6, The HPV-16 E6 protein also stimulated expression of multiple genes known to be inducible by NF-kappaB and AP-I, E6 enhanced expression of functional components of the NF-kappaB signal pathway, including p50, NIK, and TRAF-interacting protein, and increased binding to NF-kappaB and AP-I DNA consensus binding sites. Secretion of interleukin-8, RANTES, macrophage inflammatory protein la, and 10-kappa Da IFN gamma -inducible protein were increased in differentiating keratinocytes by E6, Thus, high-level expression of the HPV-16 E6 protein in differentiating keratinocytes directly alters expression of genes that influence host resistance to infection and immune function.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available