Locating and Characterizing a Transgene Integration Site by Nanopore Sequencing

The introduction of foreign DNA into cells and organisms has facilitated much of modern biological research, and it promises to become equally important in clinical practice. Locating sites of foreign DNA incorporation in mammalian genomes has proven burdensome, so the genomic location of most trans...

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Bibliographic Details
Main Authors: Nicholls, Peter K. (Author), Bellott, Daniel W. (Author), Cho, Ting-Jan (Author), Pyntikova, Tatyana (Author), Page, David C. (Author)
Other Authors: Whitehead Institute for Biomedical Research (Contributor), Massachusetts Institute of Technology. Department of Biology (Contributor)
Format: Article
Language:English
Published: Genetics Society of America, 2020-05-07T14:23:14Z.
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Online Access:Get fulltext
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100 1 0 |a Nicholls, Peter K.  |e author 
100 1 0 |a Whitehead Institute for Biomedical Research  |e contributor 
100 1 0 |a Massachusetts Institute of Technology. Department of Biology  |e contributor 
700 1 0 |a Bellott, Daniel W.  |e author 
700 1 0 |a Cho, Ting-Jan  |e author 
700 1 0 |a Pyntikova, Tatyana  |e author 
700 1 0 |a Page, David C.  |e author 
245 0 0 |a Locating and Characterizing a Transgene Integration Site by Nanopore Sequencing 
260 |b Genetics Society of America,   |c 2020-05-07T14:23:14Z. 
856 |z Get fulltext  |u https://hdl.handle.net/1721.1/125096 
520 |a The introduction of foreign DNA into cells and organisms has facilitated much of modern biological research, and it promises to become equally important in clinical practice. Locating sites of foreign DNA incorporation in mammalian genomes has proven burdensome, so the genomic location of most transgenes remains unknown. To address this challenge, we applied nanopore sequencing in search of the site of integration of Tg(Pou5f1-EGFP)2Mnn (also known as Oct4:EGFP), a widely used fluorescent reporter in mouse germ line research. Using this nanopore-based approach, we identified the site of Oct4: EGFP transgene integration near the telomere of Chromosome 9. This methodology simultaneously yielded an estimate of transgene copy number, provided direct evidence of transgene inversions, revealed contaminating E. coli genomic DNA within the transgene array, validated the integrity of neighboring genes, and enabled definitive genotyping. We suggest that such an approach provides a rapid, cost-effective method for identifying and analyzing transgene integration sites. 
520 |a Hope Funds for Cancer Research Fellow (Grant HFCR-15-06-06) 
546 |a en 
655 7 |a Article 
773 |t 10.1534/G3.119.300582 
773 |t G3