Characterization of HPV integration, viral gene expression and E6E7 alternative transcripts by RNA-Seq: A descriptive study in invasive cervical cancer
Scarce data are available on the expression of papillomavirus genome and the frequency of alternatively spliced E6E7 mRNAs in invasive cervical cancer. We carried out a comprehensive characterization of HPV expression by RNA-Seq analysis in 22 invasive cervical cancer with HPV16 or HPV18, characteri...
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Veröffentlicht in: | Genomics (San Diego, Calif.) Calif.), 2019-12, Vol.111 (6), p.1853-1861 |
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Zusammenfassung: | Scarce data are available on the expression of papillomavirus genome and the frequency of alternatively spliced E6E7 mRNAs in invasive cervical cancer. We carried out a comprehensive characterization of HPV expression by RNA-Seq analysis in 22 invasive cervical cancer with HPV16 or HPV18, characterizing the presence of integrated/episomal viral DNA, the integration sites in human genome and the proportion of alternative splicing products of E6 and E7 genes. The expression patterns suggested the presence of episomal and/or integrated viral DNA, with integration detected in most tumors, frequently occurring within human genes in HPV18+ and in intergenic regions in HPV16+ tumors. Alternative splicing of E6E7 transcripts showed E6*I as the most frequent isoform for both viral types, followed by E6*II and E6/E7 (unspliced) transcripts in HPV16+, and by E6/E7 in HPV18+ tumors. Previously described E6*VI and E6*V transcript isoforms for HPV16, and E6*X for HPV18, were rare or not detected.
•Scarce data are available on the expression of HPV genes in cervical cancer.•We characterized by RNA-Seq, the HPV16 and HPV18 expression in cervical cancer and the splicing products of E6 and E7 genes.•The analysis suggested the presence of episomal and/or integrated viral DNA, with HPV18 recurrently integrated within genes.•E6*I was most frequent transcript isoform for both viral types.•The transcripts isoforms E6*VI and E6*V for HPV16, and E6*X for HPV18, were rare or not detected. |
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ISSN: | 0888-7543 1089-8646 |
DOI: | 10.1016/j.ygeno.2018.12.008 |