Oliver Peter L, Bitoun Emmanuelle, Davies Kay E
Department of Physiology, Anatomy and Genetics, MRC Functional Genetics Unit, University of Oxford, South Parks Road, Oxford, OX1 3QX, UK.
Mamm Genome. 2007 Jul;18(6-7):412-24. doi: 10.1007/s00335-007-9014-8. Epub 2007 May 21.
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.
小鼠诱变计划的长期目标之一是培育突变品系,以促进对每个哺乳动物基因的功能研究。随着互补遗传方法与技术进步相结合,这一目标正逐渐成为现实。该策略最重要的特点之一是能够识别和比较同一基因中的多个突变,即一个等位基因系列。随着对突变文库进行基因驱动筛选的出现,寻找特定的感兴趣系列现在成为一种可行的选择。本综述着重分析来自各种基因化学诱变项目的多个突变,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作为确定基因功能的重要资源,但由于相当一部分人类疾病是由点突变引起的,识别一个等位基因系列正成为生成临床相关且功能重要的小鼠模型的同样有效的途径。