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Use of microarray hybrid capture and next-generation sequencing to identify the anatomy of a transgene
Author(s) -
Amanda J. DuBose,
Stephen T. Lichtenstein,
Narisu Narisu,
Lori L. Bonnycastle,
Amy J. Swift,
Peter S. Chines,
Francis S. Collins
Publication year - 2013
Publication title -
nucleic acids research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 9.008
H-Index - 537
eISSN - 1362-4954
pISSN - 0305-1048
DOI - 10.1093/nar/gks1463
Subject(s) - biology , transgene , bacterial artificial chromosome , genotyping , genetics , polymerase chain reaction , genome , dna sequencing , gene , computational biology , dna microarray , inverse polymerase chain reaction , microbiology and biotechnology , gene expression , nested polymerase chain reaction , genotype
Transgenic animals are extensively used to model human disease. Typically, the transgene copy number is estimated, but the exact integration site and configuration of the foreign DNA remains uncharacterized. When transgenes have been closely examined, some unexpected configurations have been found. Here, we describe a method to recover transgene insertion sites and assess structural rearrangements of host and transgene DNA using microarray hybridization and targeted sequence capture. We used information about the transgene insertion site to develop a polymerase chain reaction genotyping assay to distinguish heterozygous from homozygous transgenic animals. Although we worked with a bacterial artificial chromosome transgenic mouse line, this method can be used to analyse the integration site and configuration of any foreign DNA in a sequenced genome.

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