Effects of cellular differentiation, chromosomal integration and 5-aza-2′-deoxycytidine treatment on human papillomavirus-16 DNA methylation in cultured cell lines

• Published in: Virology (New York, N.Y.) Vol. 374; no. 2; pp. 292 - 303
• Main Authors: Kalantari, Mina, Lee, Denis, Calleja-Macias, Itzel E, Lambert, Paul F, Bernard, Hans-Ulrich
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 10-05-2008
• Subjects: Azacitidine - analogs & derivatives; Azacitidine - pharmacology; Cell Differentiation; Cervical Intraepithelial Neoplasia; Differentiation; DNA methylation; DNA Methylation - drug effects; Epithelial Cells - cytology; Epithelial Cells - virology; Extrachromosomal Inheritance - genetics; Female; HPV; Human papillomavirus 16; Human papillomavirus 16 - genetics; Human papillomavirus 16 - metabolism; Humans; Infectious Disease; Oncogene Proteins, Viral - metabolism; Papillomavirus; Papillomavirus E7 Proteins; Repressor Proteins - metabolism; Transcription; Tumor Cells, Cultured; Uterine Cervical Neoplasms; Virus Integration; Papillomavirus; DNA methylation; Transcription; Differentiation; HPV
• ISSN: 0042-6822; 1096-0341
• DOI: 10.1016/j.virol.2007.12.016

Abstract Human papillomavirus-16 (HPV-16) genomes in cell culture and in situ are affected by polymorphic methylation patterns, which can repress the viral transcription. In order to understand some of the underlying mechanisms, we investigated changes of the methylation of HPV-16 DNA in cell cultures in response to cellular differentiation, to recombination with cellular DNA, and to an inhibitor of methylation. Undifferentiated W12E cells, derived from a precancerous lesion, contained extrachromosomal HPV-16 DNA with a sporadically methylated enhancer–promoter segment. Upon W12E cell differentiation, the viral DNA was demethylated, suggesting a link between differentiation and the epigenetic state of HPV-16 DNA. The viral genomes present in two W12I clones, in which individual copies of the HPV-16 genome have integrated into cellular DNA (type 1 integrants), were unmethylated, akin to that seen in the cervical carcinoma cell line SiHa (also a type 1 integrant). This finding is consistent with hypomethylation being necessary for continued viral gene expression. In contrast, two of three type 2 integrant W12I clones, containing concatemers of HPV-16 genomes integrated into the cellular DNA contained hypermethylated viral DNA, as observed in the cervical carcinoma cell line CaSki (also a type 2 integrant). A third, type 2, W12I clone, interestingly with fewer copies of the viral genome, contained unmethylated HPV-16 genomes. Epithelial differentiation of W12I clones did not lead to demethylation of chromosomally integrated viral genomes as was seen for extrachromosomal HPV-16 DNA in W12E clones. Hypomethylation of CaSki cells in the presence of the DNA methylation inhibitor 5-aza-2′-deoxycytidine reduced the cellular viability, possibly as a consequence of toxic effects of an excess of HPV-16 gene products. Our data support a model wherein (i) the DNA methylation state of extrachromosomal HPV16 replicons and epithelial differentiation are inversely coupled during the viral life cycle, (ii) integration of the viral genome into the host chromosome events leads to an alteration in methylation patterns on the viral genome that is dependent upon the type of integration event and possibly copy number, and (iii) integration universally results in the viral DNA becoming refractory to changes in methylation state upon cellular differentiation that are observed with extrachromosomal HPV-16 genomes.