Cyclin-dependent kinases prevent DNA re-replication through multiple mechanisms

被引:369
作者
Nguyen, VQ
Co, C
Li, JJ [1 ]
机构
[1] Univ Calif San Francisco, Dept Microbiol & Immunol, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Dept Biochem & Biophys, San Francisco, CA 94143 USA
关键词
D O I
10.1038/35082600
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
The stable propagation of genetic information requires that the entire genome of an organism be faithfully replicated once and only once each cell cycle. In eukaryotes, this replication is initiated at hundreds to thousands of replication origins distributed over the genome, each of which must be prohibited from re-initiating DNA replication within every cell cycle. How cells prevent reinitiation has been a long-standing question in cell biology. In several eukaryotes, cyclin-dependent kinases (CDKs) have been implicated in promoting the block to re-initiation(1), but exactly how they perform this function is unclear. Here we show that B-type CDKs in Saccharomyces cerevisiae prevent re-initiation through multiple overlapping mechanisms, including phosphorylation of the origin recognition complex (ORC), downregulation of Cdc6 activity, and nuclear exclusion of the Mcm2-7 complex. Only when all three inhibitory pathways are disrupted do origins re-initiate DNA replication in G2/M cells. These studies show that each of these three independent mechanisms of regulation is functionally important.
引用
收藏
页码:1068 / 1073
页数:6
相关论文
共 30 条
[1]   ATP-DEPENDENT RECOGNITION OF EUKARYOTIC ORIGINS OF DNA-REPLICATION BY A MULTIPROTEIN COMPLEX [J].
BELL, SP ;
STILLMAN, B .
NATURE, 1992, 357 (6374) :128-134
[2]   THE TOPOGRAPHY OF CHROMOSOME-REPLICATION IN YEAST [J].
BREWER, BJ ;
DILLER, JD ;
FRIEDMAN, KL ;
KOLOR, KM ;
RAGHURAMAN, MK ;
FANGMAN, WL .
COLD SPRING HARBOR SYMPOSIA ON QUANTITATIVE BIOLOGY, 1993, 58 :425-434
[3]  
BROEK D, 1991, NATURE, V349, P388, DOI 10.1038/349388a0
[4]   S-PHASE-PROMOTING CYCLIN-DEPENDENT KINASES PREVENT RE-REPLICATION BY INHIBITING THE TRANSITION OF REPLICATION ORIGINS TO A PRE-REPLICATIVE STATE [J].
DAHMANN, C ;
DIFFLEY, JFX ;
NASMYTH, KA .
CURRENT BIOLOGY, 1995, 5 (11) :1257-1269
[5]   The cyclin-dependent kinase Cdc28p regulates distinct modes of Cdc6p proteolysis during the budding yeast cell cycle [J].
Drury, LS ;
Perkins, G ;
Diffley, JFX .
CURRENT BIOLOGY, 2000, 10 (05) :231-240
[6]   The Cdc4/34/53 pathway targets Cdc6p for proteolysis in budding yeast [J].
Drury, LS ;
Perkins, G ;
Diffley, JFX .
EMBO JOURNAL, 1997, 16 (19) :5966-5976
[7]   Interaction between yeast Cdc6 protein and B-type cyclin/Cdc28 kinases [J].
Elsasser, S ;
Lou, F ;
Wang, B ;
Campbell, JL ;
Jong, A .
MOLECULAR BIOLOGY OF THE CELL, 1996, 7 (11) :1723-1735
[8]   Phosphorylation controls timing of Cdc6p destruction: A biochemical analysis [J].
Elsasser, S ;
Chi, Y ;
Yang, P ;
Campbell, JL .
MOLECULAR BIOLOGY OF THE CELL, 1999, 10 (10) :3263-3277
[9]   Cell cycle regulation of human CDC6 protein - Intracellular localization, interaction with the human MCM complex, and CDC2 kinase-mediated hyperphosphorylation [J].
Fujita, M ;
Yamada, C ;
Goto, H ;
Yokoyama, N ;
Kuzushima, K ;
Inagaki, M ;
Tsurumi, T .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (36) :25927-25932
[10]   SUBCELLULAR-LOCALIZATION OF YEAST CDC46 VARIES WITH THE CELL-CYCLE [J].
HENNESSY, KM ;
CLARK, CD ;
BOTSTEIN, D .
GENES & DEVELOPMENT, 1990, 4 (12B) :2252-2263