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Relevance of BAC transgene copy number in mice: transgene copy number variation across multiple transgenic lines and correlations with transgene integrity and expression

机译:小鼠BAC转基因拷贝数的相关性:跨多个转基因品系的转基因拷贝数变异以及与转基因完整性和表达的相关性

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摘要

Bacterial artificial chromosomes (BACs) are excellent tools for manipulating large DNA fragments and, as a result, are increasingly utilized to engineer transgenic mice by pronuclear injection. The demand for BAC transgenic mice underscores the need for careful inspection of BAC integrity and fidelity following transgenesis, which may be crucial for interpreting transgene function. Thus, it is imperative that reliable methods for assessing these parameters are available. However, there are limited data regarding whether BAC transgenes routinely integrate in the mouse genome as intact molecules, how BAC transgenes behave as they are passed through the germline across successive generations, and how variation in BAC transgene copy number relates to transgene expression. To address these questions, we used TaqMan real-time PCR to estimate BAC transgene copy number in BAC transgenic embryos and lines. Here we demonstrate the reproducibility of copy number quantification with this method and describe the variation in copy number across independent transgenic lines. In addition, polymorphic marker analysis suggests that the majority of BAC transgenic lines contain intact molecules. Notably, all lines containing multiple BAC copies also contain all BAC-specific markers. Three of 23 founders analyzed contained BAC transgenes integrated into more than one genomic location. Finally, we show increased BAC transgene copy number correlates with increased BAC transgene expression. In sum, our efforts have provided a reliable method for assaying BAC transgene integrity and fidelity, and data that should be useful for researchers using BACs as transgenic vectors.
机译:细菌人工染色体(BAC)是用于操纵大DNA片段的出色工具,因此,越来越多地通过前核注射技术来利用它们来改造转基因小鼠。对BAC转基因小鼠的需求突显了转基因后对BAC完整性和保真度进行仔细检查的需求,这对于解释转基因功能可能至关重要。因此,必须有可靠的方法来评估这些参数。但是,关于BAC转基因是否作为完整分子常规整合到小鼠基因组中,BAC转基因在连续几代中通过种系传递时的行为方式以及BAC转基因拷贝数的变异与转基因表达之间的关系,目前尚缺乏有限的数据。为了解决这些问题,我们使用TaqMan实时PCR来估计BAC转基因胚胎和品系中BAC转基因的拷贝数。在这里,我们证明了这种方法的副本数量量化的可重复性,并描述了跨独立转基因品系的副本数量的变化。此外,多态性标记分析表明,大多数BAC转基因品系均包含完整分子。值得注意的是,所有包含多个BAC副本的行也都包含所有BAC特定标记。在分析的23位创建者中,有3位包含整合到一个以上基因组位置的BAC转基因。最后,我们显示增加的BAC转基因拷贝数与增加的BAC转基因表达相关。总而言之,我们的努力为测定BAC转基因的完整性和保真度提供了可靠的方法,并且该数据对于使用BAC作为转基因载体的研究人员应该是有用的。

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    《Mammalian Genome》 |2007年第10期|693-708|共16页
  • 作者单位

    Department of Molecular Physiology and Biophysics Center for Human Genetics Research Vanderbilt University School of Medicine 519 Light Hall 2215 Garland Avenue Nashville Tennessee 37232 USA;

    Department of Molecular Physiology and Biophysics Center for Human Genetics Research Vanderbilt University School of Medicine 519 Light Hall 2215 Garland Avenue Nashville Tennessee 37232 USA;

    Department of Molecular Physiology and Biophysics Center for Human Genetics Research Vanderbilt University School of Medicine 519 Light Hall 2215 Garland Avenue Nashville Tennessee 37232 USA;

    Department of Molecular Physiology and Biophysics Center for Human Genetics Research Vanderbilt University School of Medicine 519 Light Hall 2215 Garland Avenue Nashville Tennessee 37232 USA;

    Division of Genetic Medicine Department of Medicine Vanderbilt University School of Medicine 529 Light Hall 2215 Garland Avenue Nashville Tennessee 37232 USA;

    Department of Molecular Physiology and Biophysics Center for Human Genetics Research Vanderbilt University School of Medicine 519 Light Hall 2215 Garland Avenue Nashville Tennessee 37232 USA;

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