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Adenoviral vectors (AdV) are popular tools to deliver foreign genes into a wide range of cells. They have also been used in clinical gene therapy trials. Studies on AdV-mediated gene transfer to mammalian oocytes and transmission through the germ line have been reported controversially. In the present study we investigated whether AdV sequences integrate into the mouse genome by microinjecting AdV into the perivitelline space of fertilized oocytes. We applied a newly developed PCR technique (HiLo-PCR) for identification of chromosomal junctions next to the integrated AdV. We demonstrate that mouse oocytes can be transduced by different recombinant adenoviral vectors (first generation and gutless). In one transgenic mouse line using the first generation adenoviral vector, the genome has integrated into a highly repetitive cluster located on the Y chromosome. While the transgene (GFP) was expressed in early embryos, no expression was detected in adult transgenic mice. The use of gutless AdV resulted in expression of the transgene, albeit the vector was not transmitted to progeny. These results indicate that under optimized conditions fertilized mouse oocytes are transduced by AdV and give rise to transgenic founder animals. Therefore, adequate precautions should be taken in gene therapy protocols of reproductive patients since transduction of oocytes or early embryos and subsequent chromosomal integration cannot be ruled out entirely.

Original publication

DOI

10.1007/s11248-010-9401-x

Type

Journal article

Journal

Transgenic Res

Publication Date

02/2011

Volume

20

Pages

123 - 135

Keywords

Adenoviruses, Human, Animals, Antineoplastic Combined Chemotherapy Protocols, Cisplatin, Embryo, Mammalian, Female, Gene Transfer Techniques, Genetic Vectors, Green Fluorescent Proteins, Humans, Ifosfamide, Male, Mice, Mice, Inbred C57BL, Mice, Inbred DBA, Mice, Transgenic, Mitomycin, Oocytes, Recombination, Genetic, Transduction, Genetic, Transgenes, Virus Integration