Literature DB >> 21030782

ENU-based gene-driven mutagenesis in the mouse: a next-generation gene-targeting system.

Yoichi Gondo1, Ryutaro Fukumura, Takuya Murata, Shigeru Makino.   

Abstract

As a new mouse mutant resource, the RIKEN ENU-based gene-driven mutagenesis system in the mouse has been available to the research community since 2002. By using random base-substitution mutagenesis with ENU, a new reverse genetics infrastructure has been developed as a next-generation gene-targeting system. The construction of a large-scale mutant mouse library and high-throughput mutation discovery systems were the keys making it practically feasible. The RIKEN mutant mouse library consists of ~ 10,000 G1 mice, within which 100-150 mutant strains have been established based on users' requests every year. Use of the system is very simple: users 1) download an application form from our web site and send to us, and 2) design the PCR primers for the target gene. Then, we screen the RIKEN mutant mouse library and report all the detected mutations to the user. From among the allelic series of discovered mutations, users decide which mutant strain(s) to analyze and request the live mutant strain for functional studies of the target gene. Users have been reporting various functional mutations in the RIKEN mutant mouse library: e.g., missense, knockout-type and even functional non-coding mutations. In the near future, next-generation re-sequencing systems should drastically enhance the utility of the ENU-based gene-driven mutagenesis not only for the mouse but also for other species.

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Year:  2010        PMID: 21030782     DOI: 10.1538/expanim.59.537

Source DB:  PubMed          Journal:  Exp Anim        ISSN: 0007-5124


  19 in total

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Review 2.  Controlling complexity: the clinical relevance of mouse complex genetics.

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3.  Crim1C140S mutant mice reveal the importance of cysteine 140 in the internal region 1 of CRIM1 for its physiological functions.

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Journal:  Mamm Genome       Date:  2019-11-27       Impact factor: 2.957

4.  Comprehensive behavioral analysis of ENU-induced Disc1-Q31L and -L100P mutant mice.

Authors:  Hirotaka Shoji; Keiko Toyama; Yoshihiro Takamiya; Shigeharu Wakana; Yoichi Gondo; Tsuyoshi Miyakawa
Journal:  BMC Res Notes       Date:  2012-02-20

Review 5.  Genetics in non-genetic model systems.

Authors:  Carlos Lois; James O Groves
Journal:  Curr Opin Neurobiol       Date:  2011-11-24       Impact factor: 6.627

Review 6.  Disorders of sex development: new genes, new concepts.

Authors:  Makoto Ono; Vincent R Harley
Journal:  Nat Rev Endocrinol       Date:  2012-12-18       Impact factor: 43.330

7.  Defective craniofacial development and brain function in a mouse model for depletion of intracellular inositol synthesis.

Authors:  Tetsuo Ohnishi; Takuya Murata; Akiko Watanabe; Akiko Hida; Hisako Ohba; Yoshimi Iwayama; Kazuo Mishima; Yoichi Gondo; Takeo Yoshikawa
Journal:  J Biol Chem       Date:  2014-02-19       Impact factor: 5.157

Review 8.  New insights into behaviour using mouse ENU mutagenesis.

Authors:  Peter L Oliver; Kay E Davies
Journal:  Hum Mol Genet       Date:  2012-08-13       Impact factor: 6.150

9.  Functional annotation and ENU.

Authors:  Teresa M Gunn
Journal:  BMC Res Notes       Date:  2012-10-24

10.  The Mammalian Phenotype Ontology as a unifying standard for experimental and high-throughput phenotyping data.

Authors:  Cynthia L Smith; Janan T Eppig
Journal:  Mamm Genome       Date:  2012-09-09       Impact factor: 2.957

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