DONSON is required for CMG helicase assembly in the mammalian cell cycle

被引:10
|
作者
Evrin, Cecile [1 ]
Alvarez, Vanesa [2 ]
Ainsworth, Johanna [1 ]
Fujisawa, Ryo [1 ]
Alabert, Constance [2 ]
Labib, Karim P. M. [1 ]
机构
[1] Univ Dundee, Sch Life Sci, MRC Prot Phosphorylat & Ubiquitylat Unit, Dundee, Scotland
[2] Univ Dundee, Sch Life Sci, Div Mol Cell & Dev Biol, Dundee, Scotland
基金
日本学术振兴会; 欧洲研究理事会; 英国医学研究理事会;
关键词
CMG helicase; DNA replication; DONSON; initiation; Meier-Gorlin syndrome; DNA-REPLICATION; MECHANISMS; GENOME;
D O I
10.15252/embr.202357677
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
DONSON is one of 13 genes mutated in a form of primordial microcephalic dwarfism known as Meier-Gorlin syndrome. The other 12 encode components of the CDC45-MCM-GINS helicase, around which the eukaryotic replisome forms, or are factors required for helicase assembly during DNA replication initiation. A role for DONSON in CDC45-MCM-GINS assembly was unanticipated, since DNA replication initiation can be reconstituted in vitro with purified proteins from budding yeast, which lacks DONSON. Using mouse embryonic stem cells as a model for the mammalian helicase, we show that DONSON binds directly but transiently to CDC45-MCM-GINS during S-phase and is essential for chromosome duplication. Rapid depletion of DONSON leads to the disappearance of the CDC45-MCM-GINS helicase from S-phase cells and our data indicate that DONSON is dispensable for loading of the MCM2-7 helicase core onto chromatin during G1-phase, but instead is essential for CDC45-MCM-GINS assembly during S-phase. These data identify DONSON as a missing link in our understanding of mammalian chromosome duplication and provide a molecular explanation for why mutations in human DONSON are associated with Meier-Gorlin syndrome.
引用
收藏
页数:11
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