Genome Technology Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD 20892, USA.
Nucleic Acids Res. 2013 Apr 1;41(6):e70. doi: 10.1093/nar/gks1463. Epub 2013 Jan 11.
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.
转基因动物被广泛用于模拟人类疾病。通常情况下,我们会估算转基因拷贝数,但外源 DNA 的准确整合位点和结构仍未确定。当对转基因进行仔细检查时,我们发现了一些意想不到的结构。在这里,我们描述了一种使用微阵列杂交和靶向序列捕获来恢复转基因插入位点并评估宿主和转基因 DNA 结构重排的方法。我们利用转基因插入位点的信息,开发了一种聚合酶链反应基因分型检测,以区分杂合子和纯合子转基因动物。尽管我们使用的是细菌人工染色体转基因小鼠系,但这种方法可以用于分析任何已测序基因组中外源 DNA 的整合位点和结构。