Literature DB >> 20933210

Now and future of mouse mutagenesis for human disease models.

Yoichi Gondo1.   

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.
Copyright © 2010 Institute of Genetics and Developmental Biology and the Genetics Society of China. Published by Elsevier Ltd. All rights reserved.

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Year:  2010        PMID: 20933210     DOI: 10.1016/S1673-8527(09)60076-X

Source DB:  PubMed          Journal:  J Genet Genomics        ISSN: 1673-8527            Impact factor:   4.275


  5 in total

Review 1.  The role of vertebrate models in understanding craniosynostosis.

Authors:  Greg Holmes
Journal:  Childs Nerv Syst       Date:  2012-08-08       Impact factor: 1.475

2.  Method of euthanasia influences the oocyte fertilization rate with fresh mouse sperm.

Authors:  Karen C Hazzard; Dawn E Watkins-Chow; Lisa J Garrett
Journal:  J Am Assoc Lab Anim Sci       Date:  2014-11       Impact factor: 1.232

3.  PHEXL222P Mutation Increases Phex Expression in a New ENU Mouse Model for XLH Disease.

Authors:  Carole El Hakam; Alexis Parenté; Fabienne Baraige; Laetitia Magnol; Lionel Forestier; Florent Di Meo; Véronique Blanquet
Journal:  Genes (Basel)       Date:  2022-07-28       Impact factor: 4.141

4.  A new Otogelin ENU mouse model for autosomal-recessive nonsyndromic moderate hearing impairment.

Authors:  Carole El Hakam Kamareddin; Laetitia Magnol; Veronique Blanquet
Journal:  Springerplus       Date:  2015-11-25

5.  Effects of background mutations and single nucleotide polymorphisms (SNPs) on the Disc1 L100P behavioral phenotype associated with schizophrenia in mice.

Authors:  Yosefu Arime; Ryutaro Fukumura; Ikuo Miura; Kazuyuki Mekada; Atsushi Yoshiki; Shigeharu Wakana; Yoichi Gondo; Kazufumi Akiyama
Journal:  Behav Brain Funct       Date:  2014-12-08       Impact factor: 3.759

  5 in total

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