P53-DEPENDENT INHIBITION OF CYCLIN-DEPENDENT KINASE-ACTIVITIES IN HUMAN FIBROBLASTS DURING RADIATION-INDUCED G1 ARREST

被引:1460
作者
DULIC, V
KAUFMANN, WK
WILSON, SJ
TLSTY, TD
LEES, E
HARPER, JW
ELLEDGE, SJ
REED, SI
机构
[1] SCRIPPS RES INST, DEPT MOLEC BIOL MB7, LA JOLLA, CA 92037 USA
[2] UNIV N CAROLINA, LINEBERGER COMPREHENS CANC CTR, CHAPEL HILL, NC 27599 USA
[3] MASSACHUSETTS GEN HOSP, CTR CANC, MOLEC ONCOL LAB, BOSTON, MA 02129 USA
[4] BAYLOR COLL MED, INST MOLEC GENET, VERNA & MARRS MCLEAN DEPT BIOCHEM, HOUSTON, TX 77030 USA
[5] BAYLOR COLL MED, INST MOLEC GENET, HOWARD HUGHES MED INST, HOUSTON, TX 77030 USA
关键词
D O I
10.1016/0092-8674(94)90379-4
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
Gamma-irradiation of human diploid fibroblasts in the G1 interval caused arrest of the cell cycle prior to S phase. This cell cycle block was correlated with a lack of activation of both cyclin E-Cyclin-dependent kinase 2 (Cdk2) and cyclin A-Cdk2 kinases and depended on wild-type p53. Although the accumulation of cyclin A was strongly inhibited in gamma-irradiated cells, cyclin E accumulated and bound Cdk2 at normal levels but remained in an inactive state. We found that both whole-cell lysates and inactive cyclin E-Cdk2 complexes prepared from irradiated cells contained an activity capable of inactivating cyclin E-Cdk2 complexes. The protein responsible for this activity was shown to be p21CIP1/WAF1, recently described as a p53-inducible Cdk inhibitor. Our data suggest a model in which ionizing radiation confers G1 arrest via the p53-mediated induction of a Cdk inhibitor protein.
引用
收藏
页码:1013 / 1023
页数:11
相关论文
共 81 条
  • [41] LOCK RB, 1990, CANCER RES, V50, P3761
  • [42] SPECIFIC ENZYMATIC DEPHOSPHORYLATION OF THE RETINOBLASTOMA PROTEIN
    LUDLOW, JW
    GLENDENING, CL
    LIVINGSTON, DM
    DECAPRIO, JA
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 1993, 13 (01) : 367 - 372
  • [43] CELLULAR-LOCALIZATION AND CELL-CYCLE REGULATION BY A TEMPERATURE-SENSITIVE P53-PROTEIN
    MARTINEZ, J
    GEORGOFF, I
    MARTINEZ, J
    LEVINE, AJ
    [J]. GENES & DEVELOPMENT, 1991, 5 (02) : 151 - 159
  • [44] COLONY-STIMULATING FACTOR-I REGULATES NOVEL CYCLINS DURING THE G1 PHASE OF THE CELL-CYCLE
    MATSUSHIME, H
    ROUSSEL, MF
    ASHMUN, RA
    SHERR, CJ
    [J]. CELL, 1991, 65 (04) : 701 - 713
  • [45] ATAXIA-TELANGIECTASIA - AN INHERITED DISORDER OF IONIZING-RADIATION SENSITIVITY IN MAN - PROGRESS IN THE ELUCIDATION OF THE UNDERLYING BIOCHEMICAL DEFECT
    MCKINNON, PJ
    [J]. HUMAN GENETICS, 1987, 75 (03) : 197 - 208
  • [46] A FAMILY OF HUMAN CDC2-RELATED PROTEIN-KINASES
    MEYERSON, M
    ENDERS, GH
    WU, CL
    SU, LK
    GORKA, C
    NELSON, C
    HARLOW, E
    TSAI, LH
    [J]. EMBO JOURNAL, 1992, 11 (08) : 2909 - 2917
  • [47] CONDITIONAL INHIBITION OF TRANSFORMATION AND OF CELL-PROLIFERATION BY A TEMPERATURE-SENSITIVE MUTANT OF P53
    MICHALOVITZ, D
    HALEVY, O
    OREN, M
    [J]. CELL, 1990, 62 (04) : 671 - 680
  • [48] CELL-CYCLE DEPENDENT REGULATION OF PHOSPHORYLATION OF THE HUMAN RETINOBLASTOMA GENE-PRODUCT
    MIHARA, K
    CAO, XR
    YEN, A
    CHANDLER, S
    DRISCOLL, B
    MURPHREE, AL
    TANG, A
    FUNG, YKT
    [J]. SCIENCE, 1989, 246 (4935) : 1300 - 1303
  • [49] P80CDC25 MITOTIC INDUCER IS THE TYROSINE PHOSPHATASE THAT ACTIVATES P34CDC2 KINASE IN FISSION YEAST
    MILLAR, JBA
    MCGOWAN, CH
    LENAERS, G
    JONES, R
    RUSSELL, P
    [J]. EMBO JOURNAL, 1991, 10 (13) : 4301 - 4309
  • [50] REVERSIBLE TYROSINE PHOSPHORYLATION OF CDC2 - DEPHOSPHORYLATION ACCOMPANIES ACTIVATION DURING ENTRY INTO MITOSIS
    MORLA, AO
    DRAETTA, G
    BEACH, D
    WANG, JYJ
    [J]. CELL, 1989, 58 (01) : 193 - 203