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Reports

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

, , , , &
Pages 1001-1009 | Received 14 Oct 2014, Accepted 07 Jan 2015, Published online: 01 Apr 2015
 

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.

This article is referred to by:
Building up the machinery for DNA replication

Disclosure of Potential Conflicts of Interest

No potential conflicts of interest were disclosed.

Funding

This work was supported by the National Research Foundation of Korea (NRF) grants funded by the Ministry of Education, Science and Technology (no. 2011-0015907 and no. 2009-0072305).

Supplemental Material

Supplemental data for this article can be accessed on the publisher's website.

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