Regulation of cell growth-dependent expression of mammalian CDC6 gene by the cell cycle transcription factor E2F

被引:96
作者
Ohtani, K
Tsujimoto, A
Ikeda, M
Nakamura, M [1 ]
机构
[1] Tokyo Med & Dent Univ, Grad Sch Dent, Human Gene Sci Ctr, Tokyo 1138510, Japan
[2] Tokyo Med & Dent Univ, Grad Sch Dent, Dept Dev Biol, Tokyo 1138510, Japan
关键词
mammalian CDC6; E2F; promoter; cell cycle; DNA synthesis;
D O I
10.1038/sj.onc.1202105
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
CDC6 of Saccharomyces cerevisiae regulates the DNA replication initiation through the origin recognition complex (ORC), Identification of a human homolog of the CDC6 gene (HsCdc6) suggests a universal role of the gene product in DNA replication. Expression of HsCdc6 is growth-regulated. We investigated the molecular basis of growth-regulated expression of mammalian Cdc6. The promoter activity of isolated HsCdc6 upstream region was activated at late G1 and G1/S boundary in the cell cycle of rat embryonic fibroblast REF52 cells by the addition of serum. The isolated promoter was activated by exogenous expression of E2F without serum stimulation. However a mutant promoter lacking the E2F recognition sites failed to respond to serum stimulation and exogenous expression of E2F, Expression of endogenous Cdc6 was induced by exogenous expression of E2F, Therefore, we concluded that the growth-regulated expression of mammalian Cdc6 was mediated by E2F, Moreover, we demonstrated that exogenous overexpression of either HsCdc6 or HsOrc1 failed to induce DNA synthesis unlike overexpression of E2F1, even though E2F1 induced both Cdc6 and Orc1, suggesting that E2F may regulate the expression of another gene(s), besides Cdc6 and Orc1, required for induction of cellular DNA synthesis in mammalian cells.
引用
收藏
页码:1777 / 1785
页数:9
相关论文
共 46 条
[1]   Components and dynamics of DNA replication complexes in S-cerevisiae: Redistribution of MCM proteins and Cdc45p during S phase [J].
Aparicio, OM ;
Weinstein, DM ;
Bell, SP .
CELL, 1997, 91 (01) :59-69
[2]   ATP-DEPENDENT RECOGNITION OF EUKARYOTIC ORIGINS OF DNA-REPLICATION BY A MULTIPROTEIN COMPLEX [J].
BELL, SP ;
STILLMAN, B .
NATURE, 1992, 357 (6374) :128-134
[3]   THE YEAST GENE, DBF4, ESSENTIAL FOR ENTRY INTO S-PHASE IS CELL-CYCLE REGULATED [J].
CHAPMAN, JW ;
JOHNSTON, LH .
EXPERIMENTAL CELL RESEARCH, 1989, 180 (02) :419-428
[4]   Distinct roles for E2F proteins in cell growth control and apoptosis [J].
DeGregori, J ;
Leone, G ;
Miron, A ;
Jakoi, L ;
Nevins, JR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (14) :7245-7250
[5]  
DEGREGORI J, 1995, MOL CELL BIOL, V15, P4215
[6]   PROTEIN DNA INTERACTIONS AT A YEAST REPLICATION ORIGIN [J].
DIFFLEY, JFX ;
COCKER, JH .
NATURE, 1992, 357 (6374) :169-172
[7]   Cdc6p-dependent loading of Mcm proteins onto pre-replicative chromatin in budding yeast [J].
Donovan, S ;
Harwood, J ;
Drury, LS ;
Diffley, JFX .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (11) :5611-5616
[8]   INTERACTION OF DBF4, THE CDC7 PROTEIN-KINASE REGULATORY SUBUNIT, WITH YEAST REPLICATION ORIGINS IN-VIVO [J].
DOWELL, SJ ;
ROMANOWSKI, P ;
DIFFLEY, JFX .
SCIENCE, 1994, 265 (5176) :1243-1246
[9]  
Fujita M, 1996, J BIOL CHEM, V271, P4349
[10]   CONSERVED INITIATOR PROTEINS IN EUKARYOTES [J].
GAVIN, KA ;
HIDAKA, M ;
STILLMAN, B .
SCIENCE, 1995, 270 (5242) :1667-1671