Double trans-chromosomic mice: Maintenance of two individual human chromosome fragments containing Ig heavy and κ loci and expression of fully human antibodies

  • Kazuma Tomizuka
    Pharmaceutical Research Laboratory, Kirin Brewery Co., Ltd., Miyahara-cho 3, Takasaki-shi, Gunma 370-1295, Japan; and Department of Molecular and Cell Genetics, School of Life Sciences, Faculty of Medicine, Tottori University, Nishimachi 86, Yonago-shi, Tottori 683-8503, Japan
  • Tokuyuki Shinohara
    Pharmaceutical Research Laboratory, Kirin Brewery Co., Ltd., Miyahara-cho 3, Takasaki-shi, Gunma 370-1295, Japan; and Department of Molecular and Cell Genetics, School of Life Sciences, Faculty of Medicine, Tottori University, Nishimachi 86, Yonago-shi, Tottori 683-8503, Japan
  • Hitoshi Yoshida
    Pharmaceutical Research Laboratory, Kirin Brewery Co., Ltd., Miyahara-cho 3, Takasaki-shi, Gunma 370-1295, Japan; and Department of Molecular and Cell Genetics, School of Life Sciences, Faculty of Medicine, Tottori University, Nishimachi 86, Yonago-shi, Tottori 683-8503, Japan
  • Hiroshi Uejima
    Pharmaceutical Research Laboratory, Kirin Brewery Co., Ltd., Miyahara-cho 3, Takasaki-shi, Gunma 370-1295, Japan; and Department of Molecular and Cell Genetics, School of Life Sciences, Faculty of Medicine, Tottori University, Nishimachi 86, Yonago-shi, Tottori 683-8503, Japan
  • Atsuko Ohguma
    Pharmaceutical Research Laboratory, Kirin Brewery Co., Ltd., Miyahara-cho 3, Takasaki-shi, Gunma 370-1295, Japan; and Department of Molecular and Cell Genetics, School of Life Sciences, Faculty of Medicine, Tottori University, Nishimachi 86, Yonago-shi, Tottori 683-8503, Japan
  • Sonoko Tanaka
    Pharmaceutical Research Laboratory, Kirin Brewery Co., Ltd., Miyahara-cho 3, Takasaki-shi, Gunma 370-1295, Japan; and Department of Molecular and Cell Genetics, School of Life Sciences, Faculty of Medicine, Tottori University, Nishimachi 86, Yonago-shi, Tottori 683-8503, Japan
  • Kaoru Sato
    Pharmaceutical Research Laboratory, Kirin Brewery Co., Ltd., Miyahara-cho 3, Takasaki-shi, Gunma 370-1295, Japan; and Department of Molecular and Cell Genetics, School of Life Sciences, Faculty of Medicine, Tottori University, Nishimachi 86, Yonago-shi, Tottori 683-8503, Japan
  • Mitsuo Oshimura
    Pharmaceutical Research Laboratory, Kirin Brewery Co., Ltd., Miyahara-cho 3, Takasaki-shi, Gunma 370-1295, Japan; and Department of Molecular and Cell Genetics, School of Life Sciences, Faculty of Medicine, Tottori University, Nishimachi 86, Yonago-shi, Tottori 683-8503, Japan
  • Isao Ishida
    Pharmaceutical Research Laboratory, Kirin Brewery Co., Ltd., Miyahara-cho 3, Takasaki-shi, Gunma 370-1295, Japan; and Department of Molecular and Cell Genetics, School of Life Sciences, Faculty of Medicine, Tottori University, Nishimachi 86, Yonago-shi, Tottori 683-8503, Japan

抄録

<jats:p>The use of a human chromosome or its fragment as a vector for animal transgenesis may facilitate functional studies of large human genomic regions. We describe here the generation and analysis of double trans-chromosomic (Tc) mice harboring two individual human chromosome fragments (hCFs). Two transmittable hCFs, one containing the Ig heavy chain locus (<jats:italic>IgH</jats:italic>, ≈1.5 Mb) and the other the κ light chain locus (<jats:italic>Ig</jats:italic><jats:italic>κ</jats:italic>, ≈2 Mb), were introduced into a mouse strain whose endogenous<jats:italic>IgH</jats:italic>and<jats:italic>Ig</jats:italic><jats:italic>κ</jats:italic>loci were inactivated. In the resultant double-Tc/double-knockout mice, substantial proportion of the somatic cells retained both hCFs, and the rescue in the defect of Ig production was shown by high level expression of human Ig heavy and κ chains in the absence of mouse heavy and κ chains. In addition, serum expression profiles of four human Ig γ subclasses resembled those seen in humans. They mounted an antigen-specific human antibody response upon immunization with human serum albumin, and human serum albumin-specific human monoclonal antibodies with various isotypes were obtained from them. These results represent a generation of mice with “humanized” loci by using the transmittable hCFs, which suggest that the Tc technology may allow for the humanization of over megabase-sized, complex loci in mice or other animals. Such animals may be useful not only for studying<jats:italic>in vivo</jats:italic>functions of the human genome but also for obtaining various therapeutic products.</jats:p>

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