A TRANSGENIC MOUSE THAT EXPRESSES A DIVERSITY OF HUMAN SEQUENCE HEAVY AND LIGHT CHAIN IMMUNOGLOBULINS

被引:63
作者
TAYLOR, LD [1 ]
CARMACK, CE [1 ]
SCHRAMM, SR [1 ]
MASHAYEKH, R [1 ]
HIGGINS, KM [1 ]
KUO, CC [1 ]
WOODHOUSE, C [1 ]
KAY, RM [1 ]
LONBERG, N [1 ]
机构
[1] GENPHARM INT,2375 GARCIA AVE,MT VIEW,CA 94043
关键词
D O I
10.1093/nar/20.23.6287
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We have generated transgenic mice that express a diverse repertoire of human sequence immunoglobulins. The expression of this repertoire is directed by light and heavy chain minilocus transgenes comprised of human protein coding sequences in an unrearranged, germ-line configuration. In this paper we describe the construction of these miniloci and the composition of the CDR3 repertoire generated by the transgenic mice. The largest transgene discussed is a heavy chain minilocus that includes human mu and gamma1 coding sequences together with their respective switch regions. It consists of a single 61 kb DNA fragment propagated in a bacterial plasmid vector. Both human heavy chain classes are expressed in animals that carry the transgene. In light chain transgenic animals the unrearranged minilocus sequences recombine to form VJ joints that use all five human J(kappa) segments, resulting in a diversity of human-like CDR3 regions. Similarly, in heavy chain transgenics the inserted sequences undergo VDJ joining complete with N region addition to generate a human-like VH CDR3 repertoire. All six human J(H) segments and at least eight of the ten transgene encoded human D segments are expressed. The transgenic animals described in this paper represent a potential source of human sequence antibodies for in vivo therapeutic applications.
引用
收藏
页码:6287 / 6295
页数:9
相关论文
共 39 条
  • [1] HUMAN-ANTIBODY PRODUCTION IN TRANSGENIC MICE - EXPRESSION FROM 100-KB OF THE HUMAN IGH LOCUS
    BRUGGEMANN, M
    SPICER, C
    BULUWELA, L
    ROSEWELL, I
    BARTON, S
    SURANI, MA
    RABBITTS, TH
    [J]. EUROPEAN JOURNAL OF IMMUNOLOGY, 1991, 21 (05) : 1323 - 1326
  • [2] A REPERTOIRE OF MONOCLONAL-ANTIBODIES WITH HUMAN HEAVY-CHAINS FROM TRANSGENIC MICE
    BRUGGEMANN, M
    CASKEY, HM
    TEALE, C
    WALDMANN, H
    WILLIAMS, GT
    SURANI, MA
    NEUBERGER, MS
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (17) : 6709 - 6713
  • [3] REARRANGEMENT OF A CHICKEN IMMUNOGLOBULIN GENE OCCURS IN THE LYMPHOID LINEAGE OF TRANSGENIC MICE
    BUCCHINI, D
    REYNAUD, CA
    RIPOCHE, MA
    GRIMAL, H
    JAMI, J
    WEILL, JC
    [J]. NATURE, 1987, 326 (6111) : 409 - 411
  • [4] ISOLATION OF BIOLOGICALLY-ACTIVE RIBONUCLEIC-ACID FROM SOURCES ENRICHED IN RIBONUCLEASE
    CHIRGWIN, JM
    PRZYBYLA, AE
    MACDONALD, RJ
    RUTTER, WJ
    [J]. BIOCHEMISTRY, 1979, 18 (24) : 5294 - 5299
  • [5] SYNTHETIC SITES FOR TRANSCRIPTION TERMINATION AND A FUNCTIONAL COMPARISON WITH TRYPTOPHAN OPERON TERMINATION SITES INVITRO
    CHRISTIE, GE
    FARNHAM, PJ
    PLATT, T
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1981, 78 (07): : 4180 - 4184
  • [6] DERSIMONIAN H, 1989, J IMMUNOL, V142, P4027
  • [7] ENGLER P, 1991, CELL, V65, P1
  • [8] FENNEY AJ, 1990, J EXP MED, V172, P1377
  • [9] SEPARATE ELEMENTS CONTROL DJ AND VDJ REARRANGEMENT IN A TRANSGENIC RECOMBINATION SUBSTRATE
    FERRIER, P
    KRIPPL, B
    BLACKWELL, TK
    FURLEY, AJW
    SUH, HK
    WINOTO, A
    COOK, WD
    HOOD, L
    COSTANTINI, F
    ALT, FW
    [J]. EMBO JOURNAL, 1990, 9 (01) : 117 - 125
  • [10] IMMUNOGLOBULIN-KAPPA LIGHT CHAIN GENE PROMOTER AND ENHANCER ARE NOT RESPONSIBLE FOR B-CELL RESTRICTED GENE REARRANGEMENT
    GOODHARDT, M
    BABINET, C
    LUTFALLA, G
    KALLENBACH, S
    CAVELIER, P
    ROUGEON, F
    [J]. NUCLEIC ACIDS RESEARCH, 1989, 17 (18) : 7403 - 7415