Temporal and spatial regulation of eukaryotic DNA replication: From regulated initiation to genome-scale timing program

被引:34
|
作者
Renard-Guillet, Claire [1 ]
Kanoh, Yutaka [2 ]
Shirahige, Katsuhiko [1 ]
Masai, Hisao [2 ]
机构
[1] Univ Tokyo, Inst Mol & Cellular Biosci, Res Ctr Epigenet Dis, Lab Genome Struct & Funct, Tokyo 1130032, Japan
[2] Tokyo Metropolitan Inst Med Sci, Dept Genome Med, Tokyo 1568506, Japan
关键词
Replication origins; Replication timing; Pre-replicative complex; Rif1; Chromatin loop; ORIGIN RECOGNITION COMPLEX; SINGLE-STRANDED-DNA; S-PHASE CHECKPOINT; EARLY G1 PHASE; FISSION YEAST; SACCHAROMYCES-CEREVISIAE; BUDDING-YEAST; SCHIZOSACCHAROMYCES-POMBE; CHROMOSOMAL REPLICATOR; FIRING ORIGINS;
D O I
10.1016/j.semcdb.2014.04.014
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
subset of the origins is actually "fired" to initiate DNA synthesis during S phase. Whereas factors involved in these steps are relatively well understood now, the mechanisms behind the origin specification, the choice of origins to be fired and determination of their timing are still under active investigation. Recent data show that the origin positions as well as the selection of those to be fired may be determined by multiple factors including sequences, chromatin context, epigenetic information, and some specific genomic features, but that the choice is surprisingly plastic and opportunistic. Timing regulation of firing, on the other hand, appears to be related to cell type-specific intrinsic chromatin architecture in nuclei. The conserved Rifl protein appears to be a major global regulator of the genome-wide replication timing. Replication timing is regulated also by other factors including checkpoint signals, local chromatin structures, timing and quantity of pre-RC formation, and availability of limiting initiation factors.(C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:110 / 120
页数:11
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