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Volume 37 Issue 9
Sep.  2010
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Abstract
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Article Navigation >  Journal of Genetics and Genomics  > 2010  >  37(9): 559-572

Now and future of mouse mutagenesis for human disease models

doi: 10.1016/S1673-8527(09)60076-X
  •  

    Mutagenesis and Genomics Team, RIKEN BioResource Center, 3-1-1 Koyadai, Tsukuba, Ibaraki 305-0074, Japan

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  • Corresponding author: E-mail address: gondo@brc.riken.jp (Yoichi Gondo)
  • Received Date: 2010-05-26
  • Accepted Date: 2010-07-31
  • Rev Recd Date: 2010-07-30
    • Available Online: 2010-10-07
  • Publish Date: 2010-09-20
    Abstract
  • One of the major objectives of the Human Genome Project is to understand the biological function of the gene and genome as well as to develop clinical applications for human diseases. For this purpose, the experimental validations and preclinical trails by using animal models are indispensable. The mouse (Mus musculus) is one of the best animal models because genetics is well established in the mouse and embryonic manipulation technologies are also well developed. Large-scale mouse mutagenesis projects have been conducted to develop various mouse models since 1997. Originally, the phenotype-driven mutagenesis with N-ethyl-N-nitrosourea (ENU) has been the major efforts internationally then knockout/conditional mouse projects and gene-driven mutagenesis have been following. At the beginning, simple monogenic traits in the experimental condition have been elucidated. Then, more complex traits with variety of environmental interactions and gene-to-gene interactions (epistasis) have been challenged with mutant mice. In addition, chromosomal substitution strains and collaborative cross strains are also available to elucidate the complex traits in the mouse. Altogether, mouse models with mutagenesis and various laboratory strains will accelerate the studies of functional genomics in the mouse as well as in human.
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    • References(46)
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