RecQL4 is required for the association of Mcm10 and Ctf4 with replication origins in human cells Journal Article


Authors: Im, J. S.; Park, S. Y.; Cho, W. H.; Bae, S. H.; Hurwitz, J.; Lee, J. K.
Article Title: RecQL4 is required for the association of Mcm10 and Ctf4 with replication origins in human cells
Abstract: Though RecQL4 was shown to be essential for the initiation of DNA replication in mammalian cells, its role in initiation is poorly understood. Here, we show that RecQL4 is required for the origin binding of Mcm10 and Ctf4, and their physical interactions and association with replication origins are controlled by the concerted action of both CDK and DDK activities. Although RecQL4-dependent binding of Mcm10 and Ctf4 to chromatin can occur in the absence of pre-replicative complex, their association with replication origins requires the presence of the pre-replicative complex and CDK and DDK activities. Their association with replication origins and physical interactions are also targets of the DNA damage checkpoint pathways which prevent initiation of DNA replication at replication origins. Taken together, the RecQL4-dependent association of Mcm10 and Ctf4 with replication origins appears to be the first important step controlled by S phase promoting kinases and checkpoint pathways for the initiation of DNA replication in human cells. © 2015 Taylor & Francis Group, LLC.
Keywords: dna replication; mammalia; cell cycle; checkpoint; mcm10; cdk; ctf4/and-1; ddk; recql4
Journal Title: Cell Cycle
Volume: 14
Issue: 7
ISSN: 1538-4101
Publisher: Taylor & Francis Inc.  
Date Published: 2015-01-01
Start Page: 1001
End Page: 1009
Language: English
DOI: 10.1080/15384101.2015.1007001
PROVIDER: scopus
PUBMED: 25602958
PMCID: PMC4612657
DOI/URL:
Notes: Export Date: 4 May 2015 -- Source: Scopus
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  1. Jerard Hurwitz
    206 Hurwitz