MCM10 and RECQL4 have cooperative and redundant roles in activating the CMG helicase during the replication initiation

DNA replication initiation requires activation of the CMG helicase to establish the replisome. This process involves the extrusion of single-stranded DNA (ssDNA) from the central channel of MCM double hexamers, allowing the two CMG helicases to pass each other; however, the factors that mediate this process in human cells remain unclear. We show that degron-mediated depletion of either MCM10 or RECQL4 alone causes mild replication defects, whereas simultaneous depletion of both proteins severely impairs CMG activation. ChIP-seq analyses demonstrate that RECQL4 localizes to replication initiation zones (IZs) independently of MCM10, whereas MCM10 recruitment to IZs is enhanced upon RECQL4 depletion, consistent with partially redundant roles during CMG activation. Rescue experiments further indicate that RECQL4 cooperates with MCM10 through direct interaction, and that their ssDNA-binding activity underlies their functional overlap. We propose that MCM10 and RECQL4 act cooperatively and redundantly to promote CMG activation.

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Publication Details

Journal
Genes & Development
Published
2026-09-04
DOI
https://doi.org/10.1101/gad.353714.126
Citations
1
Primary Topic
DNA Repair Mechanisms
Type
preprint

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preprint

MCM10 and RECQL4 have cooperative and redundant roles in activating the CMG helicase during the replication initiation

Masato T. Kanemaki, Atsushi Toyoda, Yuki Hatoyama, Xiaoxuan Zhu et al.
1 citations
Genes & Development
DNA Repair Mechanisms
preprint

MCM10 and RECQL4 have cooperative and redundant roles in activating the CMG helicase during the replication initiation

Masato T. Kanemaki, Atsushi Toyoda, Yuki Hatoyama, Xiaoxuan Zhu, Atabek Bektash
preprint en
1 citations

Abstract

DNA replication initiation requires activation of the CMG helicase to establish the replisome. This process involves the extrusion of single-stranded DNA (ssDNA) from the central channel of MCM double hexamers, allowing the two CMG helicases to pass each other; however, the factors that mediate this process in human cells remain unclear. We show that degron-mediated depletion of either MCM10 or RECQL4 alone causes mild replication defects, whereas simultaneous depletion of both proteins severely impairs CMG activation. ChIP-seq analyses demonstrate that RECQL4 localizes to replication initiation zones (IZs) independently of MCM10, whereas MCM10 recruitment to IZs is enhanced upon RECQL4 depletion, consistent with partially redundant roles during CMG activation. Rescue experiments further indicate that RECQL4 cooperates with MCM10 through direct interaction, and that their ssDNA-binding activity underlies their functional overlap. We propose that MCM10 and RECQL4 act cooperatively and redundantly to promote CMG activation.

Genes & Development
National Institute of Genetics (JP), The Graduate University for Advanced Studies, SOKENDAI (JP), The University of Tokyo (JP)
University of Dundee, Ministry of Education, Culture, Sports, Science and Technology, Japan Society for the Promotion of Science, Japan Science and Technology Agency, Institute of Genetics, Core Research for Evolutional Science and Technology
DNA Repair Mechanisms
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