THE HUMAN FIBROBLAST GROWTH-FACTOR RECEPTOR GENES - A COMMON STRUCTURAL ARRANGEMENT UNDERLIES THE MECHANISMS FOR GENERATING RECEPTOR FORMS THAT DIFFER IN THEIR 3RD IMMUNOGLOBULIN DOMAIN

被引:395
作者
JOHNSON, DE
LU, J
CHEN, H
WERNER, S
WILLIAMS, LT
机构
[1] UNIV CALIF SAN FRANCISCO, HOWARD HUGHES MED INST, PROGRAM EXCELLENCE MOLEC BIOL, SAN FRANCISCO, CA 94143 USA
[2] UNIV CALIF SAN FRANCISCO, CARDIOVASC RES INST, SAN FRANCISCO, CA 94143 USA
关键词
D O I
10.1128/MCB.11.9.4627
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
To determine the mechanisms by which multiple forms of fibroblast growth factor (FGF) receptors are generated, we have mapped the arrangement of exons and introns in the human FGF receptor 1 (FGFR 1) gene (flg). We found three alternative exons encoding a portion of the third immunoglobulin (Ig)-like domain of the receptor. One of these alternatives encodes a sequence that is part of a secreted form of FGFR 1. The other two encode sequences that are likely part of transmembrane forms of FGFR 1. One of these forms has not been previously reported in published cDNAs. Also, we have determined the structural organization of a portion of the human FGFR 2 gene (bek) and found a similar arrangement of alternative exons for the third Ig-like domain. The arrangement of these genes suggests that there are conserved mechanisms governing the expression of secreted FGF receptors as well as the expression of at least two distinct membrane-spanning forms of the FGF receptors. The diverse forms appear to be generated by alternative splicing of mRNA and selective use of polyadenylation signals.
引用
收藏
页码:4627 / 4634
页数:8
相关论文
共 40 条
  • [1] BASIC FIBROBLAST GROWTH-FACTOR PREVENTS DEATH OF LESIONED CHOLINERGIC NEURONS INVIVO
    ANDERSON, KJ
    DAM, D
    LEE, S
    COTMAN, CW
    [J]. NATURE, 1988, 332 (6162) : 360 - 361
  • [2] AN ONCOGENE ISOLATED BY TRANSFECTION OF KAPOSIS-SARCOMA DNA ENCODES A GROWTH-FACTOR THAT IS A MEMBER OF THE FGF FAMILY
    BOVI, PD
    CURATOLA, AM
    KERN, FG
    GRECO, A
    ITTMANN, M
    BASILICO, C
    [J]. CELL, 1987, 50 (05) : 729 - 737
  • [3] BREATHNACH R, 1981, ANNU REV BIOCHEM, V50, P349, DOI 10.1146/annurev.bi.50.070181.002025
  • [4] THE HEPARIN-BINDING (FIBROBLAST) GROWTH-FACTOR FAMILY OF PROTEINS
    BURGESS, WH
    MACIAG, T
    [J]. ANNUAL REVIEW OF BIOCHEMISTRY, 1989, 58 : 575 - 606
  • [5] CLONING AND EXPRESSION OF 2 DISTINCT HIGH-AFFINITY RECEPTORS CROSS-REACTING WITH ACIDIC AND BASIC FIBROBLAST GROWTH-FACTORS
    DIONNE, CA
    CRUMLEY, G
    BELLOT, F
    KAPLOW, JM
    SEARFOSS, G
    RUTA, M
    BURGESS, WH
    JAYE, M
    SCHLESSINGER, J
    [J]. EMBO JOURNAL, 1990, 9 (09) : 2685 - 2692
  • [6] DUAN R, UNPUB
  • [7] RIBONUCLEIC-ACID ISOLATED BY CESIUM-CHLORIDE CENTRIFUGATION
    GLISIN, V
    CRKVENJAKOV, R
    BYUS, C
    [J]. BIOCHEMISTRY, 1974, 13 (12) : 2633 - 2637
  • [8] ISOLATION OF PITUITARY FIBROBLAST GROWTH-FACTOR BY FAST PROTEIN LIQUID-CHROMATOGRAPHY (FPLC) - PARTIAL CHEMICAL AND BIOLOGICAL CHARACTERIZATION
    GOSPODAROWICZ, D
    MASSOGLIA, S
    CHENG, J
    LUI, GM
    BOHLEN, P
    [J]. JOURNAL OF CELLULAR PHYSIOLOGY, 1985, 122 (02) : 323 - 332
  • [9] MOLECULAR AND BIOLOGICAL CHARACTERIZATION OF FIBROBLAST GROWTH-FACTOR, AN ANGIOGENIC FACTOR WHICH ALSO CONTROLS THE PROLIFERATION AND DIFFERENTIATION OF MESODERM AND NEUROECTODERM DERIVED CELLS
    GOSPODAROWICZ, D
    NEUFELD, G
    SCHWEIGERER, L
    [J]. CELL DIFFERENTIATION, 1986, 19 (01): : 1 - 17
  • [10] LOCALIZATION OF A FIBROBLAST GROWTH-FACTOR AND ITS EFFECT ALONE AND WITH HYDROCORTISONE ON 3T3 CELL-GROWTH
    GOSPODAROWICZ, D
    [J]. NATURE, 1974, 249 (5453) : 123 - 127