Abstract
A transgene mapping technique (Noguchi et al., Exp. Anim. 53:103-111, 2004) is described that can be used to analyze transgene integration patterns in transgenic mice. The technique was used to reveal that a transgenic mouse line (GM1-sy#116) harbored Inverted and direct tandem repeats of both intact and partial pCAGGS-based transgenes in the G2 region of chromosome 1. This complicated concatenation of transgenes may have been caused by simple end-joining of DNA constructs fragmented by exposure to UV transillumination during gel-purification, and by nuclease digestion inside zygote pronuclei. The results suggest that care should be taken to avoid unwanted fragmentation during the preparation of vector constructs. Copyright © 2006 Japanese Association for Laboratory Animal Science.
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Suzuki, O., Hata, T., Takekawa, N., Koura, M., Takano, K., Yamamoto, Y., … Matsuda, J. (2006). Transgene insertion pattern analysis using genomic walking in a transgenic mouse line. Experimental Animals, 55(1), 65–69. https://doi.org/10.1538/expanim.55.65
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