MURINE FGF-4 GENE-EXPRESSION IS SPATIALLY RESTRICTED WITHIN EMBRYONIC SKELETAL-MUSCLE AND OTHER TISSUES

被引:52
作者
DRUCKER, BJ [1 ]
GOLDFARB, M [1 ]
机构
[1] COLUMBIA UNIV COLL PHYS & SURG,DEPT BIOCHEM & MOLEC BIOPHYS,NEW YORK,NY 10032
关键词
FIBROBLAST GROWTH FACTOR; GENE EXPRESSION; MESODERM; NEUROECTODERM; SKELETAL MUSCLE;
D O I
10.1016/0925-4773(93)90073-7
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Fibroblast growth factors are believed to play many distinct roles in vertebrate development, owing to their ability to stimulate cell growth, prevent cell death, determine cell fate, and inhibit terminal differentiation in a variety of in vitro culture systems. We have used in situ hybridization to localize fibroblast growth factor-4 (FGF-4, also termed HST and K-FGF) gene expression in 7.5 to 16.5 day gestation mouse embryos. Seven discrete sites of gene expression were detected: (1) primitive streak (E7.5-8.5); (2) paraxial presomitic mesoderm in the trunk (E7.5-11.5); (3) primitive neuroectoderm (E8.0-8.5); (4) pharyngeal pouch endoderm (E8.5-9.5); (5) branchial arch ectoderm (E8.5-9.5); (6) limb apical ectoderm (E10.5-12.5), and (7) skeletal myoblast groups (E9.5-13.5). FGF-4 gene expression is spatially restricted within many of these sites. The profile of FGF-4 gene expression among skeletal muscle groups is overlapping, but distinct, from that of FGF-5, thereby revealing myoblast heterogeneity at the molecular level and suggesting distinct roles for multiple FGFs in muscle development.
引用
收藏
页码:155 / 163
页数:9
相关论文
共 37 条
  • [1] EXPRESSION OF A DOMINANT NEGATIVE MUTANT OF THE FGF RECEPTOR DISRUPTS MESODERM FORMATION IN XENOPUS EMBRYOS
    AMAYA, E
    MUSCI, TJ
    KIRSCHNER, MW
    [J]. CELL, 1991, 66 (02) : 257 - 270
  • [2] ARAKAWA Y, 1990, J NEUROSCI, V10, P3507
  • [3] A V-MYC-IMMORTALIZED SYMPATHOADRENAL PROGENITOR-CELL LINE IN WHICH NEURONAL DIFFERENTIATION IS INITIATED BY FGF BUT NOT NGF
    BIRREN, SJ
    ANDERSON, DJ
    [J]. NEURON, 1990, 4 (02) : 189 - 201
  • [4] THE MOUSE HOMOLOG OF HST
    BROOKES, S
    SMITH, R
    THURLOW, J
    DICKSON, C
    PETERS, G
    [J]. NUCLEIC ACIDS RESEARCH, 1989, 17 (11) : 4037 - 4045
  • [5] THE HEPARIN-BINDING (FIBROBLAST) GROWTH-FACTOR FAMILY OF PROTEINS
    BURGESS, WH
    MACIAG, T
    [J]. ANNUAL REVIEW OF BIOCHEMISTRY, 1989, 58 : 575 - 606
  • [6] 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
  • [7] GUILLEMOT F, 1992, DEVELOPMENT, V114, P743
  • [8] INVITRO NEURITE EXTENSION BY GRANULE NEURONS IS DEPENDENT UPON ASTROGLIAL-DERIVED FIBROBLAST GROWTH-FACTOR
    HATTEN, ME
    LYNCH, M
    RYDEL, RE
    SANCHEZ, J
    JOSEPHSILVERSTEIN, J
    MOSCATELLI, D
    RIFKIN, DB
    [J]. DEVELOPMENTAL BIOLOGY, 1988, 125 (02) : 280 - 289
  • [9] HAUB O, 1991, DEVELOPMENT, V112, P397
  • [10] EXPRESSION OF THE MURINE FIBROBLAST GROWTH FACTOR-5 GENE IN THE ADULT CENTRAL-NERVOUS-SYSTEM
    HAUB, O
    DRUCKER, B
    GOLDFARB, M
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (20) : 8022 - 8026