FUNCTIONS OF THE V-SRC PROTEIN-TYROSINE

被引:14
作者
FINCHAM, V
FRAME, M
HAEFNER, B
UNLU, M
WYKE, A
WYKE, J
机构
[1] Beatson Institute for Cancer Research Cancer Research Campaign Beatson Laboratories Garscube Estate, Glasgow, G61 1BD Scotland, Switchback Road, Bearsden
关键词
D O I
10.1006/cbir.1994.1083
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The peripheral non-receptor tyrosine kinase oncoprotein, v-Src, has pleiotropic effects. It is a mitogen for quiescent cells, substituting for both competence and progression factor-mediated signals but it also induces cellular morphological transformation. We are dissecting the activities of v-Src by studying mutant proteins, including those with temperature sensitive (ts) effects, in different cellular backgrounds. Activation of a ts v-Src kinase rapidly increases activity of both the transcription factor, AP-1, and MAP kinase, an enzyme that enhances AP-1 activity by both phosphorylation of c-Jun and increased c-fos transcription; the relative contribution of these two events depends on the cells in which v-Src is expressed. Transient early AP-1 activation requires proper location of v-Src at the cell periphery and it is essential for mitogenesis. It is not, however, sufficient for entry into S-phase, there being a second need for v-Src later in G1. Transformation by v-Src does not require AP-1 activation but seems linked to events at the cell periphery, notably phosphorylation of proteins that bind to the v-Src SH3 domain such as the p85 subunit of PI-3 kinase. © 1994 Academic Press. All rights reserved.
引用
收藏
页码:337 / 344
页数:8
相关论文
共 13 条
  • [1] TRANSFORMATION BY A TEMPERATURE SENSITIVE MUTANT OF ROUS-SARCOMA VIRUS IN ABSENCE OF SERUM
    BELL, JG
    WYKE, JA
    MACPHERSON, IA
    [J]. JOURNAL OF GENERAL VIROLOGY, 1975, 27 (MAY) : 127 - 134
  • [2] DIFFERENTIAL EXPRESSION OF ROUS-SARCOMA VIRUS-SPECIFIC TRANSFORMATION PARAMETERS IN ENUCLEATED CELLS
    BEUG, H
    CLAVIEZ, M
    JOCKUSCH, BM
    GRAF, T
    [J]. CELL, 1978, 14 (04) : 843 - 856
  • [3] THE MEMBRANE-BINDING DOMAIN AND MYRISTYLATION OF P60V-SRC ARE NOT ESSENTIAL FOR STIMULATION OF CELL-PROLIFERATION
    CALOTHY, G
    LAUGIER, D
    CROSS, FR
    JOVE, R
    HANAFUSA, T
    HANAFUSA, H
    [J]. JOURNAL OF VIROLOGY, 1987, 61 (05) : 1678 - 1681
  • [4] CATLING AD, 1993, ONCOGENE, V8, P1875
  • [5] CATLING AD, 1994, IN PRESS J VIROL
  • [6] NEITHER ARGININE NOR HISTIDINE CAN CARRY OUT THE FUNCTION OF LYSINE-295 IN THE ATP-BINDING SITE OF P60SRC
    KAMPS, MP
    SEFTON, BM
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 1986, 6 (03) : 751 - 757
  • [7] Nigg Erich A., 1993, Trends in Cell Biology, V3, P296, DOI 10.1016/0962-8924(93)90011-O
  • [8] QURESHI SA, 1992, J BIOL CHEM, V267, P17635
  • [9] A MUTATION AT THE ATP-BINDING SITE OF PP60V-SRC ABOLISHES KINASE-ACTIVITY, TRANSFORMATION, AND TUMORIGENICITY
    SNYDER, MA
    BISHOP, JM
    MCGRATH, JP
    LEVINSON, AD
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 1985, 5 (07) : 1772 - 1779
  • [10] CSK INHIBITION OF C-SRC ACTIVITY REQUIRES BOTH THE SH2 AND SH3 DOMAINS OF SRC
    SUPERTIFURGA, G
    FUMAGALLI, S
    KOEGL, M
    COURTNEIDGE, SA
    DRAETTA, G
    [J]. EMBO JOURNAL, 1993, 12 (07) : 2625 - 2634