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Helicase Activation and Establishment of Replication Forks at Chromosomal Origins of Replication
Author(s) -
Seiji Tanaka,
Hiroyuki Araki
Publication year - 2013
Publication title -
cold spring harbor perspectives in biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.011
H-Index - 173
ISSN - 1943-0264
DOI - 10.1101/cshperspect.a010371
Subject(s) - biology , origin recognition complex , pre replication complex , control of chromosome duplication , helicase , minichromosome maintenance , microbiology and biotechnology , eukaryotic dna replication , licensing factor , dna replication , cyclin dependent kinase , replication factor c , genetics , dna re replication , origin of replication , dna replication factor cdt1 , dna , cell cycle , cell , gene , rna
Many replication proteins assemble on the pre-RC-formed replication origins and constitute the pre-initiation complex (pre-IC). This complex formation facilitates the conversion of Mcm2-7 in the pre-RC to an active DNA helicase, the Cdc45-Mcm-GINS (CMG) complex. Two protein kinases, cyclin-dependent kinase (CDK) and Dbf4-dependent kinase (DDK), work to complete the formation of the pre-IC. Each kinase is responsible for a distinct step of the process in yeast; Cdc45 associates with origins in a DDK-dependent manner, whereas the association of GINS with origins depends on CDK. These associations with origins also require specific initiation proteins: Sld3 for Cdc45; and Dpb11, Sld2, and Sld3 for GINS. Functional homologs of these proteins exist in metazoa, although pre-IC formation cannot be separated by requirement of DDK and CDK because of experimental limitations. Once the replicative helicase is activated, the origin DNA is unwound, and bidirectional replication forks are established.

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