WAF1, A POTENTIAL MEDIATOR OF P53 TUMOR SUPPRESSION

被引:7847
作者
ELDEIRY, WS
TOKINO, T
VELCULESCU, VE
LEVY, DB
PARSONS, R
TRENT, JM
LIN, D
MERCER, WE
KINZLER, KW
VOGELSTEIN, B
机构
[1] JOHNS HOPKINS UNIV,SCH MED,PROGRAM HUMAN GENET & MOLEC BIOL,BALTIMORE,MD 21231
[2] NATL CTR HUMAN GENOME RES,CANC GENET LAB,BETHESDA,MD 20892
[3] THOMAS JEFFERSON UNIV,JEFFERSON CANC INST,DEPT MICROBIOL & IMMUNOL,PHILADELPHIA,PA 19107
关键词
D O I
10.1016/0092-8674(93)90500-P
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 ability of p53 to activate transcription from specific sequences suggests that genes induced by p53 may mediate its biological role as a tumor suppressor. Using a subtractive hybridization approach, we identified a gene, named WAF1, whose induction was associated with wild-type but not mutant p53 gene expression in a human brain tumor cell line. The WAF1 gene was localized to chromosome 6p21.2, and its sequence, structure, and activation by p53 was conserved in rodents. Introduction of WAF1 cDNA suppressed the growth of human brain, lung, and colon tumor cells in culture. Using a yeast enhancer trap, a p53-binding site was identified 2.4 kb upstream of WAF1 coding sequences. The WAF1 promoter, including this p53-binding site, conferred p53-dependent inducibility upon a heterologous reporter gene. These studies define a gene whose expression is directly induced by p53 and that could be an important mediator of p53-dependent tumor growth suppression.
引用
收藏
页码:817 / 825
页数:9
相关论文
共 73 条
[61]   INVIVO RECOGNITION OF A VERTEBRATE MINI-EXON AS AN EXON-INTRON-EXON UNIT [J].
STERNER, DA ;
BERGET, SM .
MOLECULAR AND CELLULAR BIOLOGY, 1993, 13 (05) :2677-2687
[62]  
TRUNT R, 1993, J BIOL CHEM, V268, P2284
[63]  
ULLRICH SJ, 1992, ONCOGENE, V7, P1635
[64]   P53 FUNCTION AND DYSFUNCTION [J].
VOGELSTEIN, B ;
KINZLER, KW .
CELL, 1992, 70 (04) :523-526
[65]   ALLELOTYPE OF COLORECTAL CARCINOMAS [J].
VOGELSTEIN, B ;
FEARON, ER ;
KERN, SE ;
HAMILTON, SR ;
PREISINGER, AC ;
NAKAMURA, Y ;
WHITE, R .
SCIENCE, 1989, 244 (4901) :207-211
[66]   THE MCK ENHANCER CONTAINS A P53 RESPONSIVE ELEMENT [J].
WEINTRAUB, H ;
HAUSCHKA, S ;
TAPSCOTT, SJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (11) :4570-4571
[67]   CONSTITUTIVE AND ENHANCED EXPRESSION FROM THE CMV MAJOR IE-PROMOTER IN A DEFECTIVE ADENOVIRUS VECTOR [J].
WILKINSON, GWG ;
AKRIGG, A .
NUCLEIC ACIDS RESEARCH, 1992, 20 (09) :2233-2239
[68]   IDENTIFICATION OF THE DNA-BINDING SITE FOR NGFI-B BY GENETIC SELECTION IN YEAST [J].
WILSON, TE ;
FAHRNER, TJ ;
JOHNSTON, M ;
MILBRANDT, J .
SCIENCE, 1991, 252 (5010) :1296-1300
[69]   THE P53 MDM-2 AUTOREGULATORY FEEDBACK LOOP [J].
WU, XW ;
BAYLE, JH ;
OLSON, D ;
LEVINE, AJ .
GENES & DEVELOPMENT, 1993, 7 (7A) :1126-1132
[70]   WILD-TYPE P53 RESTORES CELL-CYCLE CONTROL AND INHIBITS GENE AMPLIFICATION IN CELLS WITH MUTANT P53 ALLELES [J].
YIN, YX ;
TAINSKY, MA ;
BISCHOFF, FZ ;
STRONG, LC ;
WAHL, GM .
CELL, 1992, 70 (06) :937-948