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Efficient generation of long-distance conditional alleles using recombineering and a dual selection strategy in replicate plates

机译:在复制板中使用重组和双重选择策略有效生成长距离条件等位基因

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摘要

BackgroundConditional knockout mice are a useful tool to study the function of gene products in a tissue-specific or inducible manner. Classical approaches to generate targeting vectors for conditional alleles are often limited by the availability of suitable restriction sites. Furthermore, plasmid-based targeting vectors can only cover a few kB of DNA which precludes the generation of targeting vectors where the two loxP sites are placed far apart. These limitations have been overcome in the recent past by using homologous recombination of bacterial artificial chromosomes (BACs) in Escherichia coli to produce large targeting vector containing two different loxP-flanked selection cassettes so that a single targeting event is sufficient to introduce loxP-sites a great distances into the mouse genome. However, the final targeted allele should be free of selection cassettes and screening for correct removal of selection cassettes can be a laborious task. Therefore, we developed a new strategy to rapidly identify ES cells containing the desired allele.
机译:背景条件敲除小鼠是一种有用的工具,可以以组织特异性或可诱导的方式研究基因产物的功能。产生用于条件等位基因的靶向载体的经典方法通常受到合适的限制性位点的可用性的限制。此外,基于质粒的靶向载体只能覆盖几kB的DNA,从而无法生成其中两个loxP位点相距很远的靶向载体。通过使用大肠杆菌中细菌人工染色体(BAC)的同源重组产生包含两个不同loxP侧翼选择盒的大型靶向载体,克服了这些局限性,因此单个靶向事件足以引入loxP位点a距离小鼠基因组很远。但是,最终的靶向等位基因应没有选择盒,正确选择选择盒的筛查可能是一项艰巨的任务。因此,我们开发了一种新的策略来快速识别包含所需等位基因的ES细胞。

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