The ternary complex factor Net contains two distinct elements that mediate different responses to MAP kinase signalling cascades

被引:48
作者
Ducret, C [1 ]
Maira, SM [1 ]
Lutz, Y [1 ]
Wasylyk, B [1 ]
机构
[1] ULP, INSERM, CNRS, Inst Genet & Biol Mol & Cellulaire, F-67404 Illkirch Graffenstaden, France
关键词
docking; phosphorylation; Ras; transcription; repression; export;
D O I
10.1038/sj.onc.1203892
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
The ternary complex factors (TCFs), Elk-1, Sap-1a and Net, are key integrators of the transcriptional response to different signalling pathways. Classically, three MAP kinase pathways, involving ERK, JNK, and p38, transduce various extracellular stimuli to the nucleus. Net is a repressor that is converted into an activator by Ras/ERK signalling. Net is also exported from the nucleus in response to stress stimuli transduced through the JNK pathway, leading to relief from repression. Here we show that ERK and p38 bind to the D box and that binding is required for phosphorylation of the adjacent C-terminally located C-domain, The D box as web as the phosphorylation sites in the C-domain (the DC element) are required for transcription activation by Pas. On the other hand, JNK binds to the J box in the middle of the protein, and binding is required for phosphorylation of the adjacent EXport motif. Both the binding and phosphorylation sites (the JEX element) are important for Net export. In conclusion, specific targeting of Net by MAP kinase pathways involves two different docking sites and phosphorylation of two different domains. These two elements, DC and JEX, mediate two distinct functional responses.
引用
收藏
页码:5063 / 5072
页数:10
相关论文
共 46 条
  • [1] Signalling pathways: Jack of all cascades
    Cahill, MA
    Janknecht, R
    Nordheim, A
    [J]. CURRENT BIOLOGY, 1996, 6 (01) : 16 - 19
  • [2] HIGH-EFFICIENCY TRANSFORMATION OF MAMMALIAN-CELLS BY PLASMID DNA
    CHEN, C
    OKAYAMA, H
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 1987, 7 (08) : 2745 - 2752
  • [3] Net, a negative Ras-switchable TCF, contains a second inhibition domain, the CID, that mediates repression through interactions with CtBP and de-acetylation
    Criqui-Filipe, P
    Ducret, C
    Maira, SM
    Wasylyk, B
    [J]. EMBO JOURNAL, 1999, 18 (12) : 3392 - 3403
  • [4] ERK activation induces phosphorylation of Elk-1 at multiple S/T-P motifs to high stoichiometry
    Cruzalegui, FH
    Cano, E
    Treisman, R
    [J]. ONCOGENE, 1999, 18 (56) : 7948 - 7957
  • [5] DAI TN, 1995, ONCOGENE, V10, P849
  • [6] JNK1 - A PROTEIN-KINASE STIMULATED BY UV-LIGHT AND HA-RAS THAT BINDS AND PHOSPHORYLATES THE C-JUN ACTIVATION DOMAIN
    DERIJARD, B
    HIBI, M
    WU, IH
    BARRETT, T
    SU, B
    DENG, TL
    KARIN, M
    DAVIS, RJ
    [J]. CELL, 1994, 76 (06) : 1025 - 1037
  • [7] A cytoplasmic inhibitor of the JNK signal transduction pathway
    Dickens, M
    Rogers, JS
    Cavanagh, J
    Raitano, A
    Xia, ZG
    Halpern, JR
    Greenberg, ME
    Sawyers, CL
    Davis, RJ
    [J]. SCIENCE, 1997, 277 (5326) : 693 - 696
  • [8] Ducret C, 1999, MOL CELL BIOL, V19, P7076
  • [9] NET, A NEW ETS TRANSCRIPTION FACTOR THAT IS ACTIVATED BY RAS
    GIOVANE, A
    PINTZAS, A
    MAIRA, SM
    SOBIESZCZUK, P
    WASYLYK, B
    [J]. GENES & DEVELOPMENT, 1994, 8 (13) : 1502 - 1513
  • [10] TRANSCRIPTION FACTOR ATF2 REGULATION BY THE JNK SIGNAL-TRANSDUCTION PATHWAY
    GUPTA, S
    CAMPBELL, D
    DERIJARD, B
    DAVIS, RJ
    [J]. SCIENCE, 1995, 267 (5196) : 389 - 393