DNSN-1 recruits GINS for CMG helicase assembly during DNA replication initiation in Caenorhabditis elegans

被引:18
|
作者
Xia, Yisui [1 ,5 ]
Sonneville, Remi [1 ]
Jenkyn-Bedford, Michael [2 ,6 ]
Ji, Liqin [3 ]
Alabert, Constance [4 ]
Hong, Ye [1 ,3 ]
Yeeles, Joseph T. P. [2 ]
Labib, Karim P. M. [1 ]
机构
[1] Univ Dundee, Sch Life Sci, MRC Prot Phosphorylat & Ubiquitylat Unit, Dundee, Scotland
[2] MRC Lab Mol Biol, Francis Crick Ave, Cambridge, England
[3] Shandong Univ, Sch Life Sci, Shandong Prov Key Lab Anim Cell & Dev Biol, Qingdao, Peoples R China
[4] Univ Dundee, Sch Life Sci, Div Mol Cell & Dev Biol, Dundee, Scotland
[5] Shenzhen Univ, Sch Med, Guangdong Key Lab Genome Stabil & Dis Prevent, Shenzhen Univ Gen Hosp, Shenzhen, Peoples R China
[6] Rockefeller Univ, 1230 York Ave, New York, NY 10021 USA
基金
中国国家自然科学基金; 英国医学研究理事会;
关键词
CRYO-EM; POL-EPSILON; COMPLEX; FORK; SLD3; PHOSPHORYLATION; BINDING; VISUALIZATION; ACTIVATION; MECHANISMS;
D O I
10.1126/science.adi4932
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Assembly of the CMG (CDC-45-MCM-2-7-GINS) helicase is the key regulated step during eukaryotic DNA replication initiation. Until now, it was unclear whether metazoa require additional factors that are not present in yeast. In this work, we show that Caenorhabditis elegans DNSN-1, the ortholog of human DONSON, functions during helicase assembly in a complex with MUS-101/TOPBP1. DNSN-1 is required to recruit the GINS complex to chromatin, and a cryo-electron microscopy structure indicates that DNSN-1 positions GINS on the MCM-2-7 helicase motor (comprising the six MCM-2 to MCM-7 proteins), by direct binding of DNSN-1 to GINS and MCM-3, using interfaces that we show are important for initiation and essential for viability. These findings identify DNSN-1 as a missing link in our understanding of DNA replication initiation, suggesting that initiation defects underlie the human disease syndrome that results from DONSON mutations.
引用
收藏
页码:1302 / +
页数:19
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