Cell cycle regulation of DNA replication

被引:325
作者
Sclafani, R. A. [1 ]
Holzen, T. M. [1 ]
机构
[1] Univ Colorado, Sch Med, Dept Biochem & Mol Genet, Aurora, CO 80045 USA
关键词
origins; kinase; helicase; checkpoint; replisome; replicons;
D O I
10.1146/annurev.genet.41.110306.130308
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Eukaryotic DNA replication is regulated to ensure all chromosomes replicate once and only once per cell cycle. Replication begins at many origins scattered along each chromosome. Except for building yeast, origins are not defined DNA sequences and probably are inherited by epigenetic mechanisms. lnitiation at origins occurs throughout the S phase according to a temporal program that is important in regulating gene expression during development. Most replication proteins are conserved in evolution in eukaryotes and archaea, but not in bacteria. However, the mechanism of initiation is conserved and consists of origin recognition, assembly of pre-replication (pre-RC) initiative complexes, helicase activation, and replisome loading. Cell cycle regulation by protein phosphorylation ensures that pre-RC assembly can only occur in G1 phase, whereas helicase activation and loading can only occur in S phase. Checkpoint regulation maintains high fidelity by stabilizing replication forks and preventing cell cycle progression during replication stress or damage.
引用
收藏
页码:237 / 280
页数:44
相关论文
共 324 条
[1]   A globular complex formation by Nda1 and the other five members of the MCM protein family in fission yeast [J].
Adachi, Y ;
Usukura, J ;
Yanagida, M .
GENES TO CELLS, 1997, 2 (07) :467-479
[2]   Chromatin regulates origin activity in Drosophila follicle cells [J].
Aggarwal, BD ;
Calvi, BR .
NATURE, 2004, 430 (6997) :372-376
[3]   Mrc1 transduces signals of DNA replication stress to activate Rad53 [J].
Alcasabas, AA ;
Osborn, AJ ;
Bachant, J ;
Hu, FH ;
Werler, PJH ;
Bousset, K ;
Furuya, K ;
Diffley, JFX ;
Carr, AM ;
Elledge, SJ .
NATURE CELL BIOLOGY, 2001, 3 (11) :958-965
[4]   Cdc2-cyclin E complexes regulate the G1/S phase transition [J].
Aleem, E ;
Kiyokawa, H ;
Kaldis, P .
NATURE CELL BIOLOGY, 2005, 7 (08) :831-U93
[5]   Characterization of simian virus 40 T-antigen double hexamers bound to a replication fork - The active form of the helicase [J].
Alexandrov, AI ;
Botchan, MR ;
Cozzarelli, NR .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (47) :44886-44897
[6]  
ALFANO C, 1989, J BIOL CHEM, V264, P10709
[7]  
ALFANO C, 1989, J BIOL CHEM, V264, P10699
[8]  
[Anonymous], 2007, CELL CYCLE
[9]  
[Anonymous], 2005, DNA REPAIR MUTAGENES
[10]   Differential assembly of Cdc45p and DNA polymerases at early and late origins of DNA replication [J].
Aparicio, OM ;
Stout, AM ;
Bell, SP .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (16) :9130-9135