Tessarollo Lino, Palko Mary Ellen, Akagi Keiko, Coppola Vincenzo
Mouse Cancer Genetics Program, NCI-Frederick, Frederick, MD, USA.
Methods Mol Biol. 2009;530:141-64. doi: 10.1007/978-1-59745-471-1_8.
The scientific value of a mouse model with a targeted mutation depends greatly upon how carefully the mutation has been engineered. Until recently, our ability to alter the mouse genome has been limited by both the lack of technologies to conditionally target a locus and by conventional cloning. The "cre/loxP" and "recombineering" technologies have overcome some of these limitations and have greatly enhanced our ability to manipulate the mouse genome in a sophisticated way. However, there are still some practical aspects that need to be considered to successfully target a specific genetic locus. Here, we describe the process to engineer a targeted mutation to generate a mouse model. We include a tutorial using the publicly available informatic tools that can be downloaded for processing the genetic information needed to generate a targeting vector.
具有靶向突变的小鼠模型的科学价值在很大程度上取决于突变构建的精细程度。直到最近,我们改变小鼠基因组的能力一直受到条件性靶向基因座技术的缺乏以及传统克隆方法的限制。“cre/loxP”和“重组工程”技术克服了其中一些限制,并极大地增强了我们以复杂方式操纵小鼠基因组的能力。然而,要成功靶向特定基因座,仍有一些实际问题需要考虑。在此,我们描述构建靶向突变以生成小鼠模型的过程。我们提供了一个教程,介绍如何使用可公开下载的信息工具来处理生成靶向载体所需的遗传信息。