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

被引:145
作者
Tomizuka, K
Shinohara, T
Yoshida, H
Uejima, H
Ohguma, A
Tanaka, S
Sato, K
Oshimura, M
Ishida, I
机构
[1] Kirin Brewery Co Ltd, Pharmaceut Res Lab, Takasaki, Gumma 3701295, Japan
[2] Tottori Univ, Fac Med, Sch Life Sci, Dept Mol & Cell Genet, Yonago, Tottori 6838503, Japan
关键词
D O I
10.1073/pnas.97.2.722
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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 (IgH, approximate to 1.5 Mb) and the other the kappa light chain locus (Ig kappa c, approximate to 2 Mb), were introduced into a mouse strain whose endogenous IgH and Ig kappa 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 kappa chains in the absence of mouse heavy and kappa chains. In addition, serum expression profiles of four human Ig gamma 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 he useful not only for studying in vivo functions of the human genome but also for obtaining various therapeutic products.
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页码:722 / 727
页数:6
相关论文
共 26 条
  • [1] Cloned transgenic calves produced from nonquiescent fetal fibroblasts
    Cibelli, JB
    Stice, SL
    Golueke, PJ
    Kane, JJ
    Jerry, J
    Blackwell, C
    de Leon, FAP
    Robl, JM
    [J]. SCIENCE, 1998, 280 (5367) : 1256 - 1258
  • [2] Human/mouse homology relationships
    DeBry, RW
    Seldin, MF
    [J]. GENOMICS, 1996, 33 (03) : 337 - 351
  • [3] Deursoen J.V., 1995, P NATL ACAD SCI USA, V92, P7376
  • [4] BIOLOGICAL BASIS OF GERMLINE MUTATION - COMPARISONS OF SPONTANEOUS GERMLINE MUTATION-RATES AMONG DROSOPHILA, MOUSE, AND HUMAN
    DROST, JB
    LEE, WR
    [J]. ENVIRONMENTAL AND MOLECULAR MUTAGENESIS, 1995, 25 : 48 - 64
  • [5] High-avidity human IgG kappa monoclonal antibodies from a novel strain of minilocus transgenic mice
    Fishwild, DM
    ODonnell, SL
    Bengoechea, T
    Hudson, DV
    Harding, F
    Bernhard, SL
    Jones, D
    Kay, RM
    Higgins, KM
    Schramm, SR
    Lonberg, N
    [J]. NATURE BIOTECHNOLOGY, 1996, 14 (07) : 845 - 851
  • [6] Engineering mammalian chromosomes
    Grimes, B
    Cooke, H
    [J]. HUMAN MOLECULAR GENETICS, 1998, 7 (10) : 1635 - 1640
  • [7] Transchromosomal mouse embryonic stem cell lines and chimeric mice that contain freely segregating segments of human chromosome 21
    Hernandez, D
    Mee, PJ
    Martin, JE
    Tybulewicz, VLJ
    Fisher, EMC
    [J]. HUMAN MOLECULAR GENETICS, 1999, 8 (05) : 923 - 933
  • [8] Human huntingtin derived from YAC transgenes compensates for loss of murine huntingtin by rescue of the embryonic lethal phenotype
    Hodgson, JG
    Smith, DJ
    McCutcheon, K
    Koide, HB
    Nishiyama, K
    Dinulos, MB
    Stevens, ME
    Bissada, N
    Nasir, J
    Kanazawa, I
    Disteche, CM
    Rubin, EM
    Hayden, MR
    [J]. HUMAN MOLECULAR GENETICS, 1996, 5 (12) : 1875 - 1885
  • [9] DISTRIBUTION OF CENP-B BOXES REFLECTED IN CREST CENTROMERE ANTIGENIC SITES ON LONG-RANGE ALPHA-SATELLITE DNA ARRAYS OF HUMAN-CHROMOSOME-21
    IKENO, M
    MASUMOTO, H
    OKAZAKI, T
    [J]. HUMAN MOLECULAR GENETICS, 1994, 3 (08) : 1245 - 1257
  • [10] ISLAM KB, 1994, J IMMUNOL, V152, P1442