Transcriptional activation of the human proliferating-cell nuclear antigen promoter by p53

被引:125
作者
Morris, GF [1 ]
Bischoff, JR [1 ]
Mathews, MB [1 ]
机构
[1] COLD SPRING HARBOR LAB, COLD SPRING HARBOR, NY 11724 USA
关键词
D O I
10.1073/pnas.93.2.895
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Proliferating-cell nuclear antigen (PCNA) is a DNA damage-inducible protein that performs an essential function in DNA replication and repair as an auxiliary factor for DNA polymerases delta and epsilon. Examination of the human PCNA promoter DNA sequence revealed a site with homology to the consensus DNA sequence bound by p53. PCNA promoter fragments with this site intact bound p53 in vitro and were transcriptionally activated by wild-type p53 in transient expression assays in SAOS-2 cells. The resident p53-binding site could be functionally substituted by a previously described p53-binding site from the ribosomal gene cluster. A plasmid expressing a mutated version of p53 derived from a patient with Li-Fraumeni syndrome failed to activate the PCNA promoter in the cotransfection assay. In different cell types, activation of the PCNA promoter by the p53-binding sequence correlated with the status of p53. Activation of the PCNA promoter by wild-type p53 depends upon the level of p53 expression. This concentration dependence and cell type specificity reconciles the observations presented here with prior results indicating that wild-type p53 represses the PCNA promoter. These findings provide a mechanism whereby p53 modulates activation of PCNA expression as a cellular response to DNA damage.
引用
收藏
页码:895 / 899
页数:5
相关论文
共 64 条
[51]   PROLIFERATING CELL NUCLEAR ANTIGEN IS REQUIRED FOR DNA EXCISION REPAIR [J].
SHIVJI, MKK ;
KENNY, MK ;
WOOD, RD .
CELL, 1992, 69 (02) :367-374
[52]   TRANSCRIPTIONAL ACTIVATION BY SP1 AS DIRECTED THROUGH TATA OR INITIATOR - SPECIFIC REQUIREMENT FOR MAMMALIAN TRANSCRIPTION FACTOR-IID [J].
SMALE, ST ;
SCHMIDT, MC ;
BERK, AJ ;
BALTIMORE, D .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (12) :4509-4513
[53]   INTERACTION OF THE P53-REGULATED PROTEIN GADD45 WITH PROLIFERATING CELL NUCLEAR ANTIGEN [J].
SMITH, ML ;
CHEN, IT ;
ZHAN, QM ;
BAE, IS ;
CHEN, CY ;
GILMER, TM ;
KASTAN, MB ;
OCONNOR, PM ;
FORNACE, AJ .
SCIENCE, 1994, 266 (5189) :1376-1380
[54]   IDENTIFICATION OF THE GUANINE-NUCLEOTIDE DISSOCIATION STIMULATOR FOR RAL AS A PUTATIVE EFFECTOR MOLECULE OF R-RAS, H-RAS, K-RAS, AND RAP [J].
SPAARGAREN, M ;
BISCHOFF, JR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (26) :12609-12613
[55]  
SRIVASTAVA S, 1993, ONCOGENE, V8, P2449
[56]   INHIBITION OF VIRAL AND CELLULAR PROMOTERS BY HUMAN WILD-TYPE P53 [J].
SUBLER, MA ;
MARTIN, DW ;
DEB, S .
JOURNAL OF VIROLOGY, 1992, 66 (08) :4757-4762
[57]   P53 FUNCTION AND DYSFUNCTION [J].
VOGELSTEIN, B ;
KINZLER, KW .
CELL, 1992, 70 (04) :523-526
[58]   THE P21 INHIBITOR OF CYCLIN-DEPENDENT KINASES CONTROLS DNA-REPLICATION BY INTERACTION WITH PCNA [J].
WAGA, S ;
HANNON, GJ ;
BEACH, D ;
STILLMAN, B .
NATURE, 1994, 369 (6481) :574-578
[59]   INCREASED AND ALTERED DNA-BINDING OF HUMAN P53 BY S AND G2/M BUT NOT G1 CYCLIN-DEPENDENT KINASES [J].
WANG, Y ;
PRIVES, C .
NATURE, 1995, 376 (6535) :88-91
[60]   SUBUNIT REARRANGEMENT OF THE CYCLIN-DEPENDENT KINASES IS ASSOCIATED WITH CELLULAR-TRANSFORMATION [J].
XIONG, Y ;
ZHANG, H ;
BEACH, D .
GENES & DEVELOPMENT, 1993, 7 (08) :1572-1583