Fibroblast growth factor signaling in Caenorhabditis elegans

被引:42
作者
Borland, CZ [1 ]
Schutzman, JL [1 ]
Stern, MJ [1 ]
机构
[1] Yale Univ, Sch Med, Dept Genet, New Haven, CT 06520 USA
关键词
D O I
10.1002/bies.10007
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
Growth factor receptor tyrosine kinases (RTKs), such as the fibroblast growth factor receptor (FGFR), play a major role in how cells communicate with their environment. FGFR signaling is crucial for normal development, and its misregulation in humans has been linked to developmental abnormalities and cancer. The precise molecular mechanisms by which FGFRs transduce extracellular signals to eff ect specific biologic responses is an area of intense research. Genetic analyses in model organisms have played a central role in our evolving understanding of these signal transduction cascades. Genetic studies in the nematode C. elegans have contributed to our knowledge of FGFR signaling by identifying genes involved in FGFR signal transduction and linking their gene products together into signaling modules. This review will describe FGFR-mediated signal transduction in C. elegans and focus on how these studies have contributed to our understanding of how FGFRs orchestrate the assembly of intracellular signaling pathways. (C) 2001 John Wiley & Sons, Inc.
引用
收藏
页码:1120 / 1130
页数:11
相关论文
共 86 条
  • [41] Lin XH, 1999, DEVELOPMENT, V126, P3715
  • [42] THE SH2 AND SH3 DOMAIN CONTAINING PROTEIN GRB2 LINKS RECEPTOR TYROSINE KINASES TO RAS SIGNALING
    LOWENSTEIN, EJ
    DALY, RJ
    BATZER, AG
    LI, W
    MARGOLIS, B
    LAMMERS, R
    ULLRICH, A
    SKOLNIK, EY
    BARSAGI, D
    SCHLESSINGER, J
    [J]. CELL, 1992, 70 (03) : 431 - 442
  • [43] Michelson AM, 1998, DEVELOPMENT, V125, P4379
  • [44] A TYROSINE-PHOSPHORYLATED CARBOXY-TERMINAL PEPTIDE OF THE FIBROBLAST GROWTH-FACTOR RECEPTOR (FLG) IS A BINDING-SITE FOR THE SH2 DOMAIN OF PHOSPHOLIPASE C-GAMMA-1
    MOHAMMADI, M
    HONEGGER, AM
    ROTIN, D
    FISCHER, R
    BELLOT, F
    LI, W
    DIONNE, CA
    JAYE, M
    RUBINSTEIN, M
    SCHLESSINGER, J
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 1991, 11 (10) : 5068 - 5078
  • [45] POINT MUTATION IN FGF RECEPTOR ELIMINATES PHOSPHATIDYLINOSITOL HYDROLYSIS WITHOUT AFFECTING MITOGENESIS
    MOHAMMADI, M
    DIONNE, CA
    LI, W
    LI, N
    SPIVAK, T
    HONEGGER, AM
    JAYE, M
    SCHLESSINGER, J
    [J]. NATURE, 1992, 358 (6388) : 681 - 684
  • [46] Structure of the FGF receptor tyrosine kinase domain reveals a novel autoinhibitory mechanism
    Mohammadi, M
    Schlessinger, J
    Hubbard, SR
    [J]. CELL, 1996, 86 (04) : 577 - 587
  • [47] Mohammadi M, 1996, MOL CELL BIOL, V16, P977
  • [48] A phosphatidylinositol-3-OH kinase family member regulating longevity and diapause in Caenorhabditis elegans
    Morris, JZ
    Tissenbaum, HA
    Ruvkun, G
    [J]. NATURE, 1996, 382 (6591) : 536 - 539
  • [49] BASIC FIBROBLAST GROWTH-FACTOR AND FIBROBLAST GROWTH-FACTOR RECEPTOR-I ARE IMPLICATED IN THE GROWTH OF HUMAN ASTROCYTOMAS
    MORRISON, RS
    YAMAGUCHI, F
    SAYA, H
    BRUNER, JM
    YAHANDA, AM
    DONEHOWER, LA
    BERGER, M
    [J]. JOURNAL OF NEURO-ONCOLOGY, 1994, 18 (03) : 207 - 216
  • [50] FUNCTIONAL-STUDY OF THE CAENORHABDITIS-ELEGANS SECRETORY-EXCRETORY SYSTEM USING LASER MICROSURGERY
    NELSON, FK
    RIDDLE, DL
    [J]. JOURNAL OF EXPERIMENTAL ZOOLOGY, 1984, 231 (01): : 45 - 56