Characterization of Sleeping Beauty Transposition and Its Application to Genetic Screening in Mice

Author:

Horie Kyoji12,Yusa Kosuke2,Yae Kojiro23,Odajima Junko4,Fischer Sylvia E. J.5,Keng Vincent W.26,Hayakawa Tomoko2,Mizuno Sumi26,Kondoh Gen2,Ijiri Takashi7,Matsuda Yoichi78,Plasterk Ronald H. A.5,Takeda Junji126

Affiliation:

1. Collaborative Research Center for Advanced Science and Technology

2. Department of Social and Environmental Medicine

3. Division of Gene Function in Animals, Nara Institute of Science and Technology, Ikoma, Nara 630-0101

4. Department of Hematology and Oncology

5. Hubrecht Laboratory, Center for Biomedical Genetics, 3584 CT Utrecht, The Netherlands

6. Japan Science and Technology Corporation, Graduate School of Medicine, Osaka University, Suita, Osaka 565-0871

7. Laboratory of Cytogenetics, Division of Bioscience, Graduate School of Environmental Earth Science

8. Laboratory of Animal Cytogenetics, Center for Advanced Science and Technology, Hokkaido University, Kita-ku, Sapporo 060-0810, Japan

Abstract

ABSTRACT The use of mutant mice plays a pivotal role in determining the function of genes, and the recently reported germ line transposition of the Sleeping Beauty ( SB ) transposon would provide a novel system to facilitate this approach. In this study, we characterized SB transposition in the mouse germ line and assessed its potential for generating mutant mice. Transposition sites not only were clustered within 3 Mb near the donor site but also were widely distributed outside this cluster, indicating that the SB transposon can be utilized for both region-specific and genome-wide mutagenesis. The complexity of transposition sites in the germ line was high enough for large-scale generation of mutant mice. Based on these initial results, we conducted germ line mutagenesis by using a gene trap scheme, and the use of a green fluorescent protein reporter made it possible to select for mutant mice rapidly and noninvasively. Interestingly, mice with mutations in the same gene, each with a different insertion site, were obtained by local transposition events, demonstrating the feasibility of the SB transposon system for region-specific mutagenesis. Our results indicate that the SB transposon system has unique features that complement other mutagenesis approaches.

Publisher

American Society for Microbiology

Subject

Cell Biology,Molecular Biology

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