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Development and validation of a novel reporter assay for human papillomavirus type 16 late gene expression.

J Virol Methods.. 2012-08;  183(2):106-16
OrrÙ B, Cunniffe C, Ryan F, Schwartz S. Dublin Institute of Technology, Kevin Street, Dublin 8, Ireland
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摘要

To facilitate the investigations of HPV-16 late gene expression HPV-16 reporter plasmids were generated using previously described sub-genomic HPV-16 plasmids, named pBEL and pBELM, that, similar to the full viral genome, produce primarily HPV-16 early mRNAs and very little, if any, late mRNAs in cervical cancer cells. The HPV-16 late L1 gene was replaced by the chloramphenicol acetyltransferase (CAT) reporter gene, or green fluorescent protein (GFP), preceded by the poliovirus internal ribosome entry site (IRES). Results show that the reporter genes mimic the expression of L1 from these plasmids. For example, overexpression of adenovirus E4orf4 protein (E4orf4), polypyrimidine tract binding protein (PTB), argi... More

关键词

HPV-16; Splicing; hnRNP A2/B1; TPA; ASF/SF2; SR proteins; Novel reporter assay