Differential assembly of Cdc45p and DNA polymerases at early and late origins of DNA replication

被引:187
作者
Aparicio, OM [1 ]
Stout, AM [1 ]
Bell, SP [1 ]
机构
[1] MIT, Dept Biol, Cambridge, MA 02139 USA
关键词
D O I
10.1073/pnas.96.16.9130
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
Chromosomes are replicated in characteristic, temporal patterns during S phase. We have compared the timing of association of replication proteins at early- and Late-replicating origins of replication. Minichromosome maintenance proteins assemble simultaneously at early- and late-replicating origins. In contrast, Cdc45p association with late origins is delayed relative to early origins. DNA polymerase alpha association is similarly delayed at late origins and requires Cdc45p function. Activation of the S phase checkpoint inhibits association of Cdc45p with late-firing origins. These studies suggest that Cdc45p is poised to serve as a key regulatory target for both the temporal and checkpoint-mediated regulation of replication origins.
引用
收藏
页码:9130 / 9135
页数:6
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