DNA replication and progression through S phase

被引:156
作者
Takeda, DY
Dutta, A [1 ]
机构
[1] Harvard Univ, Sch Med, Brigham & Womens Hosp, Dept Pathol, Boston, MA 02115 USA
[2] Univ Virginia, Dept Biochem & Mol Genet, Charlottesville, VA 22908 USA
关键词
cell cycle; S phase; DNA replication;
D O I
10.1038/sj.onc.1208616
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
Initiation and completion of DNA replication defines the beginning and ending of S phase of the cell cycle. Successful progression through S phase requires that replication be properly regulated and monitored to ensure that the entire genome is duplicated exactly once, without errors, in a timely fashion. Given the immense size and complexity of eukaryotic genomes, this presents a significant challenge for the cell. As a result, DNA replication has evolved into a tightly regulated process involving the coordinated action of numerous factors that function in all phases of the cell cycle. We will review our current understanding of these processes from the formation of prereplicative complexes in preparation for S phase to the series of events that culminate in the loading of DNA polymerases during S phase. We will incorporate structural data from archaeal and bacterial replication proteins and discuss their implications for understanding the mechanism of action of their corresponding eukaryotic homologues. We will also describe the concept of replication licensing which protects against genomic instability by limiting initiation events to once per cell cycle. Lastly, we will review our knowledge of checkpoint pathways that maintain the integrity of stalled forks and relay defects in replication to the rest of the cell cycle.
引用
收藏
页码:2827 / 2843
页数:17
相关论文
共 261 条
[11]   ATP-DEPENDENT RECOGNITION OF EUKARYOTIC ORIGINS OF DNA-REPLICATION BY A MULTIPROTEIN COMPLEX [J].
BELL, SP ;
STILLMAN, B .
NATURE, 1992, 357 (6374) :128-134
[12]   Synthesis and turn-over of the replicative Cdc6 protein during the HeLa cell cycle [J].
Biermann, E ;
Baack, M ;
Kreitz, S ;
Knippers, R .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 2002, 269 (03) :1040-1046
[13]   Replication licensing - defining the proliferative state? [J].
Blow, JJ ;
Hodgson, B .
TRENDS IN CELL BIOLOGY, 2002, 12 (02) :72-78
[14]   Replication origins in Xenopus egg extract are 5-15 kilobases apart and are activated in clusters that fire at different times [J].
Blow, JJ ;
Gillespie, PJ ;
Francis, D ;
Jackson, DA .
JOURNAL OF CELL BIOLOGY, 2001, 152 (01) :15-25
[15]   The Cdc7 protein kinase is required for origin firing during S phase [J].
Bousset, K ;
Diffley, JFX .
GENES & DEVELOPMENT, 1998, 12 (04) :480-490
[16]   INITIATION PREFERENCE AT A YEAST ORIGIN OF REPLICATION [J].
BREWER, BJ ;
FANGMAN, WL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (08) :3418-3422
[17]  
BROEK D, 1991, NATURE, V349, P388, DOI 10.1038/349388a0
[18]  
Brown EJ, 2000, GENE DEV, V14, P397
[19]   Cell cycle regulation of Dfp1, an activator of the Hsk1 protein kinase [J].
Brown, GW ;
Kelly, TJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (15) :8443-8448
[20]   Purification of Hsk1, a minichromosome maintenance protein kinase from fission yeast [J].
Brown, GW ;
Kelly, TJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (34) :22083-22090