Gondo Yoichi, Fukumura Ryutaro, Murata Takuya, Makino Shigeru
Mutagenesis and Genomics Team, RIKEN BioResource Center, 3-1-1 Koyadai, Tsukuba, Ibaraki 305-0074, Japan
BMB Rep. 2009 Jun 30;42(6):315-23. doi: 10.5483/bmbrep.2009.42.6.315.
In order to elucidate ultimate biological function of the genome, the model animal system carrying mutations is indispensable. Recently, large-scale mutagenesis projects have been launched in various species. Especially, the mouse is considered to be an ideal model to human because it is a mammalian species accompanied with well-established genetic as well as embryonic technologies. In 1990's, large-scale mouse mutagenesis projects firstly initiated with a potent chemical mutagen, N-ethyl-N-nitrosourea (ENU) by the phenotype-driven approach or forward genetics. The knockout mouse mutagenesis projects with trapping/conditional mutagenesis have then followed as Phase II since 2006 by the gene-driven approach or reverse genetics. Recently, the next-generation gene targeting system has also become available to the research community, which allows us to establish and analyze mutant mice carrying an allelic series of base substitutions in target genes as another reverse genetics. Overall trends in the large-scale mouse mutagenesis will be reviewed in this article particularly focusing on the new advancement of the next-generation gene targeting system. The drastic expansion of the mutant mouse resources altogether will enhance the systematic understanding of the life. The construction of the mutant mouse resources developed by the forward and reverse genetic mutagenesis is just the beginning of the annotation of mammalian genome. They provide basic infrastructure to understand the molecular mechanism of the gene and genome and will contribute to not only basic researches but also applied sciences such as human disease modelling, genomic medicine and personalized medicine.
为了阐明基因组的最终生物学功能,携带突变的模式动物系统不可或缺。最近,已在各种物种中启动了大规模诱变项目。特别是,小鼠被认为是人类的理想模型,因为它是一种哺乳动物,拥有成熟的遗传学和胚胎技术。在20世纪90年代,大规模小鼠诱变项目首先通过表型驱动方法或正向遗传学,利用强效化学诱变剂N-乙基-N-亚硝基脲(ENU)启动。自2006年以来,采用基因驱动方法或反向遗传学的捕获/条件诱变敲除小鼠诱变项目作为第二阶段随后开展。最近,下一代基因靶向系统也已可供研究界使用,这使我们能够建立和分析在靶基因中携带一系列等位基因碱基替换的突变小鼠,作为另一种反向遗传学方法。本文将综述大规模小鼠诱变的总体趋势,特别关注下一代基因靶向系统的新进展。突变小鼠资源的急剧扩展将共同增强对生命的系统理解。通过正向和反向遗传诱变开发的突变小鼠资源的构建仅仅是哺乳动物基因组注释的开始。它们为理解基因和基因组的分子机制提供了基础设施,不仅将有助于基础研究,还将有助于诸如人类疾病建模、基因组医学和个性化医学等应用科学。