Genomic insertion of lentiviral DNA circles directed by the yeast Flp recombinase

Rafael J Yáñez-Muñoz, Brian Moldt, Maria Jakobsen and Jacob G Mikkelsen

(2008)

Rafael J Yáñez-Muñoz, Brian Moldt, Maria Jakobsen and Jacob G Mikkelsen (2008) Genomic insertion of lentiviral DNA circles directed by the yeast Flp recombinase. BMC Biotechnology , 8 (60). pp. . ISSN 1472-6750

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Abstract

Background Circular forms of viral genomic DNA are generated during infection of cells with retroviruses like HIV-1. Such circles are unable to replicate and are eventually lost as a result of cell division, lending support to the prevalent notion that episomal retroviral DNA forms are dead-end products of reverse transcription. Results We demonstrate that circular DNA generated during transduction with HIV-1-based lentiviral vectors can be utilized as substrate for gene insertion directed by nonviral recombinases co-expressed in the target cells. By packaging of lentiviral genomic RNA in integrase-defective lentiviral vectors, harboring an inactive form of the viral integrase, the normal pathway for viral integration is blocked and circular vector DNA accumulates in transduced cells as a result. We find that the amount of DNA circles is increased 4-fold in cells transduced with integration-defective vectors relative to cells treated with integrase-proficient vectors. By transduction of target cells harboring engineered recognition sites for the yeast Flp recombinase with integration-defective lentiviral vectors containing an ATG-deficient hygromycin B selection gene we demonstrate precise integration of lentiviral vector-derived DNA circles in a drug-selective approach. Moreover, it is demonstrated that trans-acting Flp recombinase can be delivered by Flp-encoding transfected plasmid DNA or, alternatively, by co-transduced integrase-defective lentiviral vectors carrying a Flp expression cassette. Conclusion Our data provide proof-of-principle that nonviral recombinases, like Flp, produced by plasmid DNA or non-integrating lentiviral vectors can gain access to circular viral recombination substrates and facilitate site-directed genomic insertion of such episomal DNA forms. Replacement of the normal viral integration machinery with nonviral mediators of integration represents a new platform for creation of lentiviral vectors with an altered integration profile.

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This is a Published version
This version's date is: 09/08/2008
This item is peer reviewed

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https://repository.royalholloway.ac.uk/items/6e42db16-f4b0-40c1-3de8-d306c0a4cc81/1/

Item TypeJournal Article
TitleGenomic insertion of lentiviral DNA circles directed by the yeast Flp recombinase
AuthorsYáñez-Muñoz, Rafael
Moldt, Brian
Jakobsen, Maria
Mikkelsen, Jacob
DepartmentsFaculty of Science\Biological Science

Identifiers

doi10.1186/1472-6750-8-60

Deposited by () on 24-Jan-2011 in Royal Holloway Research Online.Last modified on 25-Jan-2011

Notes

© 2008 Moldt et al; licensee BioMed Central Ltd.
This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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