Nucleic Acids Research, Vol 24, Issue 11 1999-2004, Copyright © 1996 by Oxford University Press
V Frances and M Bastin
We used the recombination-promoting activity of the polyomavirus large T
antigen (T-ag) to increase the frequency of gene targeting in rat
fibroblasts. We constructed a cell line carrying a functional polyomavirus
replication origin and a transformation-defective middle T- ag oncogene.
The structure of the locus was such that homologous recombination with the
targeting DNA reconstituted a functional transforming gene and converted
the cells from the normal to the transformed state. Introduction of the
large T-ag with the targeting DNA promoted recombinational events that
corrected the mutation in either the target locus or the targeting DNA. The
frequency of recombination was not substantially influenced by the extent
of homology between the recombining sequences. However, it was reduced when
the replication origin was inactivated in the targeting DNA, and was
reduced further when the origin was inactivated in the target locus.
ARTICLES
Gene targeting in rat embryo fibroblasts promoted by the polyomavirus large T antigen
Department of Biochemistry, Universite de Sherbrooke, Sherbrooke, Quebec, Canada.
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