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Effects of deletion of the ac109 gene of Autographa californica nucleopolyhedrovirus on interactions with mammalian cells

Resumen
Baculoviruses are able to enter into mammalian cells, where they can express a transgene that is placed under an appropriate promoter, without producing infectious progeny. ORF109 encodes an essential baculovirus protein that participates in the interaction of the baculovirus with mammalian cells. To date, the mechanisms underlying this interaction are not yet known. We demonstrated that although a Ac109 knock out virus maintained its ability to enter [ver mas...]
Baculoviruses are able to enter into mammalian cells, where they can express a transgene that is placed under an appropriate promoter, without producing infectious progeny. ORF109 encodes an essential baculovirus protein that participates in the interaction of the baculovirus with mammalian cells. To date, the mechanisms underlying this interaction are not yet known. We demonstrated that although a Ac109 knock out virus maintained its ability to enter into BHK-21 cells, there was a marked reduction in the expression efficiency of the nuclear transgene. Moreover, the amount of free cytoplasmic viral DNA, which was detected by transcription of a reporter gene, was severely diminished. These results suggest Ac109 could be involved in maintaining the integrity of the viral nucleic acid. [Cerrar]
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Autor
Alfonso, Victoria;   Amalfi, Sabrina;   Lopez, Maria Gabriela;   Taboga, Oscar Alberto;  
Fuente
Archives of virology 162 (3) : 835–840. (March 2017)
Fecha
2017-03
ISSN
0304-8608 (Print)
1432-8798 (Online)
URI
http://hdl.handle.net/20.500.12123/1350
https://link.springer.com/article/10.1007/s00705-016-3142-y
DOI
https://doi.org/10.1007/s00705-016-3142-y
Formato
pdf
Tipo de documento
artículo
Palabras Claves
Genética; Genetics; Autographa Californica; Baculovirus; Genes;
Derechos de acceso
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Excepto donde se diga explicitamente, este item se publica bajo la siguiente descripción: Creative Commons Attribution-NonCommercial-ShareAlike 2.5 Unported (CC BY-NC-SA 2.5)
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