Regulated TRESLIN-MTBP loading governs initiation zones and replication timing in human DNA replication

Replication origins in human cells form clusters ranging from tens to hundreds of kilobases called initiation zones (IZs), typically located in intergenic regions between active genes. On a larger megabase scale, chromosomes replicate following temporally defined replication timing (RT), where euchromatic regions replicate early, and heterochromatic regions replicate late. Although the stochastic model of IZ firing with a temporally regulated limiting factor can explain RT formation, this limiting factor in human cells remains unclear. To investigate the relationship between IZ and RT, we map the temporal firing pattern of IZs and examine the genome-wide distributions of replication licensing and firing factors in human cells. We identify TRESLIN-MTBP as a key limiting firing factor for replication initiation. Its loading onto phosphorylated MCM2-7 double hexamer (MCM-DH) is controlled by the opposing phosphorylation events on MCM-DH by Dbf4-dependent kinase and RIF1-Protein Phosphatase 1, which ultimately determine IZs and establish RT.

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Publication Details

Journal
Nature Communications
Published
2025-12-02
DOI
https://doi.org/10.1038/s41467-025-66278-7
Citations
1
Primary Topic
DNA Repair Mechanisms
Type
article
Field-Weighted Citation Impact
0.81
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article

Regulated TRESLIN-MTBP loading governs initiation zones and replication timing in human DNA replication

Shin-Ya Isobe, Masato T. Kanemaki, Atsushi Toyoda, Chikashi Obuse et al.
1 citations
Nature Communications
DNA Repair Mechanisms
0.81
article

Regulated TRESLIN-MTBP loading governs initiation zones and replication timing in human DNA replication

Shin-Ya Isobe, Masato T. Kanemaki, Atsushi Toyoda, Chikashi Obuse, Yuki Hatoyama, Sachiko Muramatsu, Chun-Long Chen, Yasukazu Daigaku, Xiaoxuan Zhu, Atabek Bektash
article en
1 citations

Abstract

Replication origins in human cells form clusters ranging from tens to hundreds of kilobases called initiation zones (IZs), typically located in intergenic regions between active genes. On a larger megabase scale, chromosomes replicate following temporally defined replication timing (RT), where euchromatic regions replicate early, and heterochromatic regions replicate late. Although the stochastic model of IZ firing with a temporally regulated limiting factor can explain RT formation, this limiting factor in human cells remains unclear. To investigate the relationship between IZ and RT, we map the temporal firing pattern of IZs and examine the genome-wide distributions of replication licensing and firing factors in human cells. We identify TRESLIN-MTBP as a key limiting firing factor for replication initiation. Its loading onto phosphorylated MCM2-7 double hexamer (MCM-DH) is controlled by the opposing phosphorylation events on MCM-DH by Dbf4-dependent kinase and RIF1-Protein Phosphatase 1, which ultimately determine IZs and establish RT.

Nature CommunicationsVol. 16(1)
National Institute of Genetics (JP), Centre National de la Recherche Scientifique (FR), The Graduate University for Advanced Studies, SOKENDAI (JP), Université Paris Sciences et Lettres (FR), China South Industries Group (China) (CN), Sorbonne Université (FR), Dynamique de l'information génétique : bases fondamentales et cancer (FR), Research Organization of Information and Systems (JP), Japanese Foundation For Cancer Research (JP), The University of Tokyo (JP), The University of Osaka (JP)
Openalex Percentile: Top 21%
DNA Repair Mechanisms
0.81
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