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dc.contributor.authorARECHAGA 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.issued2010-
dc.identifier.urihttp://ilitia.cua.uam.mx:8080/jspui/handle/123456789/43-
dc.description.abstractThe 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 pRben_US
dc.language.isoInglésen_US
dc.publisherArch Virol (2010) 155:1959–1970en_US
dc.rightshttps://www.academia.edu/8709101/The_HPV16_E7_oncoprotein_is_expressed_mainly_from_the_unspliced_E6_E7_transcript_in_cervical_carcinoma_C33-A_cells-
dc.rightshttps://doi.org/10.1007/s00705-010-0787-9-
dc.subjectCélulas Cancerígenasen_US
dc.subjectCánceren_US
dc.subjectTumoresen_US
dc.titleThe HPV-16 E7 oncoprotein is expressed mainly from the unspliced E6/E7 transcript in cervical carcinoma C33-A cellsen_US
dc.typeArtículoen_US
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