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Comparative genetic analysis: the utility of mouse genetic systems for studying human monogenic disease

机译:比较遗传分析:小鼠遗传系统在研究人类单基因疾病中的作用

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摘要

One of the long-term goals of mutagenesis programs in the mouse has been to generate mutant lines to facilitate the functional study of every mammalian gene. With a combination of complementary genetic approaches and advances in technology, this aim is slowly becoming a reality. One of the most important features of this strategy is the ability to identify and compare a number of mutations in the same gene, an allelic series. With the advent of gene-driven screening of mutant archives, the search for a specific series of interest is now a practical option. This review focuses on the analysis of multiple mutations from chemical mutagenesis projects in a wide variety of genes and the valuable functional information that has been obtained from these studies. Although gene knockouts and transgenics will continue to be an important resource to ascertain gene function, with a significant proportion of human diseases caused by point mutations, identifying an allelic series is becoming an equally efficient route to generating clinically relevant and functionally important mouse models.
机译:小鼠诱变程序的长期目标之一是产生突变株,以促进每个哺乳动物基因的功能研究。通过互补的遗传方法和技术进步的结合,这一目标正逐渐成为现实。该策略最重要的特征之一是能够识别和比较同一基因(一个等位基因系列)中的许多突变。随着突变档案的基因驱动筛选的出现,寻找一个特定的感兴趣的序列现在已成为一种实用的选择。这篇综述着重于分析来自多种基因的化学诱变项目中的多个突变,以及从这些研究中获得的有价值的功能信息。尽管基因敲除和转基因将继续成为确定基因功能的重要资源,但是由于点突变引起的人类疾病占很大比例,但是鉴定等位基因系列正成为产生具有临床意义和功能重要的小鼠模型的同等有效途径。

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