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Functional Characterization of Transgene Integration Patterns by Halo Fluorescence in Situ Hybridization:  Electroporation versus Retroviral Infection

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GBF-German Research Center for Biotechnology/Epigenetic Regulation, Mascheroder Weg 1, D-38124 Braunschweig, Germany
Cite this: Biochemistry 2003, 42, 23, 7035–7043
Publication Date (Web):May 17, 2003
https://doi.org/10.1021/bi0340907
Copyright © 2003 American Chemical Society

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    Abstract

    Gene transfer techniques are essential for bioengineering and gene therapy. Retroviral vectors constitute an important tool in this context as integrase-catalyzed genomic anchoring is one of the best defined results of nonhomologous recombination, occurring at loci with favorable expression properties. On the basis of a retroviral expression cassette, this study focuses on differences regarding the genomic targets after its transfer by either retroviral infection or electroporation. Fluorescence in situ hybridization (FISH) of clones generated by infection revealed for the majority an association of the transgene with the nuclear matrix while this was true only for a minority of single copy clones if the same construct was transferred by electroporation. Our results demonstrate that the process of integration is distinct for both gene transfer routes and confirm that retroviral survival strategies favor integration next to scaffold/matrix attachment regions. These results may be one key to explain recent consequences of gene therapy trials that have led to the deregulation of endogenous genes.

     This work was supported by a grant from the Deutsche Forschungsgemeinschaft (Bo 419/6) and BMBF Grant 01 KW 0003.

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     To whom correspondence should be addressed. E-mail:  [email protected]. Tel:  +49 531 6181 251. Fax:  +49 531 6181 262.

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