Myc suppresses induction of the growth arrest genes gadd34, gadd45, and gadd153 by DNA-damaging agents

被引:78
作者
Amundson, SA
Zhan, Q
Penn, LZ
Fornace, AJ
机构
[1] NCI, NIH, Bethesda, MD 20892 USA
[2] Univ Toronto, Ontario Canc Inst, Dept Med Biophys, Toronto, ON M5G 2M9, Canada
关键词
gadd45; myc; transcriptional repression;
D O I
10.1038/sj.onc.1202136
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 growth arrest and DNA damage inducible (gadd) genes are induced by various genotoxic and nongenotoxic stresses such as serum starvation, ultraviolet irradiation and treatment with alkylating agents. Their coordinate induction is a growth arrest signal which may play an important role in the response of cells to DNA damage. Conversely, c-myc is a strong proliferative signal, and overexpression of Myc is frequently observed in cancer cells, We have found that ectopic expression of v-myc in RAT-I cells results in an attenuated induction of the three major gadd transcripts by methyl methanesulfonate (MMS), and almost completely blocks the response to ultraviolet (UV) radiation. Myc acts in part by reducing the stress-responsiveness of the gadd45 promoter, as a c-myc expression vector strongly suppressed activation of gadd-reporter constructs. This activity of Myc localizes to a recently described CC-rich binding site within the gadd45 promoter. These results indicate that a coordinate down-regulation of the gadd gene response is one mechanism by which Myc can circumvent growth arrest and contribute to the neoplastic phenotype.
引用
收藏
页码:2149 / 2154
页数:6
相关论文
共 28 条
  • [1] ORNITHINE DECARBOXYLASE ACTIVITY IS CRITICAL FOR CELL-TRANSFORMATION
    AUVINEN, M
    PAASINEN, A
    ANDERSSON, LC
    HOLTTA, E
    [J]. NATURE, 1992, 360 (6402) : 355 - 358
  • [2] Chen CH, 1996, ONCOGENE, V13, P1659
  • [3] CHOMCZYNSKI P, 1987, ANAL BIOCHEM, V162, P156, DOI 10.1016/0003-2697(87)90021-2
  • [4] The Myc negative autoregulation mechanism requires Myc-Max association and involves the c-myc P2 minimal promoter
    Facchini, LM
    Chen, SJ
    Marhin, WW
    Lear, JN
    Penn, LZ
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 1997, 17 (01) : 100 - 114
  • [5] DNA DAMAGE-INDUCIBLE TRANSCRIPTS IN MAMMALIAN-CELLS
    FORNACE, AJ
    ALAMO, I
    HOLLANDER, MC
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (23) : 8800 - 8804
  • [6] MAMMALIAN GENES COORDINATELY REGULATED BY GROWTH ARREST SIGNALS AND DNA-DAMAGING AGENTS
    FORNACE, AJ
    NEBERT, DW
    HOLLANDER, MC
    LUETHY, JD
    PAPATHANASIOU, M
    FARGNOLI, J
    HOLBROOK, NJ
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 1989, 9 (10) : 4196 - 4203
  • [7] FORNACE AJ, 1992, ANNU REV GENET, V26, P507
  • [8] CDC25 PHOSPHATASES AS POTENTIAL HUMAN ONCOGENES
    GALAKTIONOV, K
    LEE, AK
    ECKSTEIN, J
    DRAETTA, G
    MECKLER, J
    LODA, M
    BEACH, D
    [J]. SCIENCE, 1995, 269 (5230) : 1575 - 1577
  • [9] HERMEKING H, 1995, ONCOGENE, V11, P1409
  • [10] MEDIATION OF C-MYC-INDUCED APOPTOSIS BY P53
    HERMEKING, H
    EICK, D
    [J]. SCIENCE, 1994, 265 (5181) : 2091 - 2093