THE MOUSE FAS-LIGAND GENE IS MUTATED IN GLD MICE AND IS PART OF A TNF FAMILY GENE-CLUSTER

被引:325
作者
LYNCH, DH
WATSON, ML
ALDERSON, MR
BAUM, PR
MILLER, RE
TOUGH, T
GIBSON, M
DAVISSMITH, T
SMITH, CA
HUNTER, K
BHAT, D
DIN, W
GOODWIN, RG
SELDIN, MF
机构
[1] DUKE UNIV,CTR AUTOIMMUNE GENET,DEPT MICROBIOL,DIV RHEUMATOL,DURHAM,NC 27710
[2] DUKE UNIV,DEPT MED,DURHAM,NC 27710
[3] IMMUNEX RES & DEV CORP,DEPT CELLULAR IMMUNOL,SEATTLE,WA 98101
[4] IMMUNEX RES & DEV CORP,DEPT MOLEC BIOL,SEATTLE,WA 98101
[5] IMMUNEX RES & DEV CORP,DEPT MAMMALIAN CELL DEV,SEATTLE,WA 98101
[6] IMMUNEX RES & DEV CORP,DEPT BIOCHEM,SEATTLE,WA 98101
[7] MIT,CTR CANC RES,CAMBRIDGE,MA 02139
关键词
D O I
10.1016/1074-7613(94)90106-6
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The gene for the mouse Fas ligand was cloned and its chromosomal position determined. Fasl was tightly linked to gld (no crossovers in 567 meiotic events) on mouse chromosome 1 and closely linked with a novel member of the same TNF family of ligands, the Ox40 ligand (Ox40l, 1 crossover in 567 meiotic events). Southern blot analysis did not reveal any difference between the Fasl gene from gld and wild-type mice and levels of Fasl mRNA transcripts were similar in PMA and ionomycin induced wild-type and coisogenic gld T cells. Sequence analysis of the gld gene indicated a single amino acid change(Phe Leu) in the COOH terminal portion of this type II transmembrane protein, and COS cells transfected with Fasl cDNA from gld mice failed to induce apoptosis of pas-expressing target cells. Thus, the data demonstrate that the gld phenotype is the result of a point mutation in the Fasl gene and that Fasl is part of a complex of ligands structurally related to TNF mapping within a small region of mouse chromosome 1.
引用
收藏
页码:131 / 136
页数:6
相关论文
共 31 条
  • [1] FAS TRANSDUCES ACTIVATION SIGNALS IN NORMAL HUMAN T-LYMPHOCYTES
    ALDERSON, MR
    ARMITAGE, RJ
    MARASKOVSKY, E
    TOUGH, TW
    ROUX, E
    SCHOOLEY, K
    RAMSDELL, F
    LYNCH, DH
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1993, 178 (06) : 2231 - 2235
  • [2] DIFFERENCES DEFINED BY BONE-MARROW TRANSPLANTATION SUGGEST THAT LPR AND GLD ARE MUTATIONS OF GENES ENCODING AN INTERACTING PAIR OF MOLECULES
    ALLEN, RD
    MARSHALL, JD
    ROTHS, JB
    SIDMAN, CL
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1990, 172 (05) : 1367 - 1375
  • [3] BLANK RD, 1988, GENETICS, V120, P1073
  • [4] BROWNING JL, 1991, J IMMUNOL, V147, P1230
  • [5] LYMPHOTOXIN-BETA, A NOVEL MEMBER OF THE TNF FAMILY THAT FORMS A HETEROMERIC COMPLEX WITH LYMPHOTOXIN ON THE CELL-SURFACE
    BROWNING, JL
    NGAMEK, A
    LAWTON, P
    DEMARINIS, J
    TIZARD, R
    CHOW, EPC
    HESSION, C
    OBRINEGRECO, B
    FOLEY, SF
    WARE, CF
    [J]. CELL, 1993, 72 (06) : 847 - 856
  • [6] CAMERINI D, 1991, J IMMUNOL, V147, P3165
  • [7] LPR AND GLD - SINGLE GENE MODELS OF SYSTEMIC AUTOIMMUNITY AND LYMPHOPROLIFERATIVE DISEASE
    COHEN, PL
    EISENBERG, RA
    [J]. ANNUAL REVIEW OF IMMUNOLOGY, 1991, 9 : 243 - 269
  • [8] MOLECULAR-CLONING AND EXPRESSION OF A NEW MEMBER OF THE NERVE GROWTH-FACTOR RECEPTOR FAMILY THAT IS CHARACTERISTIC FOR HODGKINS-DISEASE
    DURKOP, H
    LATZA, U
    HUMMEL, M
    EITELBACH, F
    SEED, B
    STEIN, H
    [J]. CELL, 1992, 68 (03) : 421 - 427
  • [9] ETTINGER R, 1993, J IMMUNOL, V152, P1557
  • [10] A TECHNIQUE FOR RADIOLABELING DNA RESTRICTION ENDONUCLEASE FRAGMENTS TO HIGH SPECIFIC ACTIVITY
    FEINBERG, AP
    VOGELSTEIN, B
    [J]. ANALYTICAL BIOCHEMISTRY, 1983, 132 (01) : 6 - 13