LUPUS SUSCEPTIBILITY LOCI IN NEW-ZEALAND MICE

被引:301
作者
KONO, DH [1 ]
BURLINGAME, RW [1 ]
OWENS, DG [1 ]
KURAMOCHI, A [1 ]
BALDERAS, RS [1 ]
BALOMENOS, D [1 ]
THEOFILOPOULOS, AN [1 ]
机构
[1] Scripps Res Inst, DEPT IMMUNOL, LA JOLLA, CA 92037 USA
关键词
MICROSATELLITES; SUSCEPTIBIIITY GENES;
D O I
10.1073/pnas.91.21.10168
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
Susceptibility to systemic lupus erythematosus has been uuequivocally established to be an inherited trait, but the exact genes and how they confer susceptibility remain largely unknown. In this study of(NZB x NZW)F-2 intercross mice, we used linkage analysis of markers covering >90% of the autosomal genome and identified eight susceptibility loci (Lbw1 to -8, chromosomes 17, 4-7, 18, 1, 11, respectively) associated with antichromatin autoantibody production, glomerulonephritis, and/or mortality. Only one locus, the major histocompatibility complex, was linked to all three traits. Two other loci were associated with both glomerulonephritis and mortality, whereas the remaining loci were linked to one of the above traits. Two additional loci (Sbw1 and -2) that contributed to splenomegaly were also identified. The Sbw2 locus mapped to the identical region as Lbw2, a locus on chromosome 4 linked to glomerulonephritis and mortality, suggesting a single locus with pleiotropic effects. The results indicate that the immunopathologic features of lupus are affected by distinct, but additive, genetic contributions. Studies to determine the nature of the genes associated with these loci should help define the genetic mechanisms involved in this systemic autoimmune disease.
引用
收藏
页码:10168 / 10172
页数:5
相关论文
共 25 条
  • [1] SPONTANEOUS MURINE LUPUS-LIKE SYNDROMES - CLINICAL AND IMMUNOPATHOLOGICAL MANIFESTATIONS IN SEVERAL STRAINS
    ANDREWS, BS
    EISENBERG, RA
    THEOFILOPOULOS, AN
    IZUI, S
    WILSON, CB
    MCCONAHEY, PJ
    MURPHY, ED
    ROTHS, JB
    DIXON, FJ
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1978, 148 (05) : 1198 - 1215
  • [2] GENESIS AND EVOLUTION OF ANTICHROMATIN AUTOANTIBODIES IN MURINE LUPUS IMPLICATES T-DEPENDENT IMMUNIZATION WITH SELF ANTIGEN
    BURLINGAME, RW
    RUBIN, RL
    BALDERAS, RS
    THEOFILOPOULOS, AN
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1993, 91 (04) : 1687 - 1696
  • [3] DIETRICH W, 1992, GENETICS, V131, P423
  • [4] GENETIC-ANALYSIS OF THE NZB CONTRIBUTION TO LUPUS-LIKE AUTOIMMUNE-DISEASE IN (NZB X NZW)F-1 MICE
    DRAKE, CG
    BABCOCK, SK
    PALMER, E
    KOTZIN, BL
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (09) : 4062 - 4066
  • [5] POLYGENIC CONTROL OF AUTOIMMUNE DIABETES IN NONOBESE DIABETIC MICE
    GHOSH, S
    PALMER, SM
    RODRIGUES, NR
    CORDELL, HJ
    HEARNE, CM
    CORNALL, RJ
    PRINS, JB
    MCSHANE, P
    LATHROP, GM
    PETERSON, LB
    WICKER, LS
    TODD, JA
    [J]. NATURE GENETICS, 1993, 4 (04) : 404 - 409
  • [6] HIROSE S, 1986, EUR J IMMUNOL, V16, P1631, DOI 10.1002/eji.1830161226
  • [7] HIROSE S, 1984, CLIN EXP IMMUNOL, V58, P694
  • [8] CONTRIBUTION OF THE GENE LINKED TO THE T-CELL RECEPTOR BETA-CHAIN GENE-COMPLEX OF NZW MICE TO THE AUTOIMMUNITY OF (NZB X NZW)F1 MICE
    HIROSE, S
    TOKUSHIGE, K
    KINOSHITA, K
    NOZAWA, S
    SAITO, J
    NISHIMURA, H
    SHIRAI, T
    [J]. EUROPEAN JOURNAL OF IMMUNOLOGY, 1991, 21 (03) : 823 - 826
  • [9] GENETIC DISSECTION OF AUTOIMMUNE TYPE-I DIABETES IN THE BB RAT
    JACOB, HJ
    PETTERSSON, A
    WILSON, D
    MAO, Y
    LERNMARK, A
    LANDER, ES
    [J]. NATURE GENETICS, 1992, 2 (01) : 56 - 60
  • [10] POLYCLONAL-B CELL ACTIVATION IN LUPUS-PRONE MICE PRECEDES AND PREDICTS THE DEVELOPMENT OF AUTOIMMUNE-DISEASE
    KLINMAN, DM
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1990, 86 (04) : 1249 - 1254