DC Field | Value | Language |
dc.contributor.author | ARECHAGA OCAMPO, ELENA | - |
dc.coverage.spatial | <dc:creator id="info:eu-repo/dai/mx/cvu/40111">ELENA ARECHAGA OCAMPO</dc:creator> | - |
dc.coverage.temporal | <dc:subject>info:eu-repo/classification/cti/2</dc:subject> | - |
dc.date.issued | 2010 | - |
dc.identifier.uri | http://ilitia.cua.uam.mx:8080/jspui/handle/123456789/43 | - |
dc.description.abstract | The HPV-16 E6/E7 early transcripts are first produced as bicistronic or polycistronic mRNAs, and about 90% of the original pre-mRNA is spliced to produce three new alternative mRNAs. HPV-16 spliced transcripts are expressed heterogeneously in tumors and cell lines. Our results suggest that suboptimal splicing acceptor sites in E6/E7 intron 1 and the differential expression of splicing factors are involved in the production of the heterogeneous splicing profile in cell lines. The unspliced pre-mRNA and the alternative spliced transcripts contribute differentially to the production of E7 in stably transfected C33-A cells. The highest level of E7 was produced from the least prevalent transcript, the unspliced E6/E7pre-mRNA. The order of relative expression of E7 was unspliced E6/E7pre-mRNA[E6*I/E7[ E6*II/E7. Our findings suggest that E6/E7 alternative splicing may be a mechanism for differential expression of the E6 and E7 oncoproteins, which also affects the expression of their targets, the proteins p53 and pRb | en_US |
dc.language.iso | Inglés | en_US |
dc.publisher | Arch Virol (2010) 155:1959–1970 | en_US |
dc.rights | https://www.academia.edu/8709101/The_HPV16_E7_oncoprotein_is_expressed_mainly_from_the_unspliced_E6_E7_transcript_in_cervical_carcinoma_C33-A_cells | - |
dc.rights | https://doi.org/10.1007/s00705-010-0787-9 | - |
dc.subject | Células Cancerígenas | en_US |
dc.subject | Cáncer | en_US |
dc.subject | Tumores | en_US |
dc.title | The HPV-16 E7 oncoprotein is expressed mainly from the unspliced E6/E7 transcript in cervical carcinoma C33-A cells | en_US |
dc.type | Artículo | en_US |
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