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An Essential and Cell-Cycle-Dependent ORC Dimerization Cycle Regulates Eukaryotic Chromosomal DNA Replication
Author(s) -
Aftab Amin,
Rentian Wu,
Man Hei Cheung,
John F. Scott,
Ziyi Wang,
Zijing Zhou,
Changdong Liu,
Guang Zhu,
Chris K.C. Wong,
ZhiLing Yu,
Chun Liang
Publication year - 2020
Publication title -
cell reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.264
H-Index - 154
eISSN - 2639-1856
pISSN - 2211-1247
DOI - 10.1016/j.celrep.2020.02.046
Subject(s) - cell cycle , dna replication , microbiology and biotechnology , eukaryotic dna replication , origin recognition complex , control of chromosome duplication , replication (statistics) , dna , licensing factor , cell cycle checkpoint , biology , s phase , eukaryotic cell , dna re replication , chemistry , genetics , cell , virology
Eukaryotic DNA replication licensing is a prerequisite for, and plays a role in, regulating genome duplication that occurs exactly once per cell cycle. ORC (origin recognition complex) binds to and marks replication origins throughout the cell cycle and loads other replication-initiation proteins onto replication origins to form pre-replicative complexes (pre-RCs), completing replication licensing. However, how an asymmetric single-heterohexameric ORC structure loads the symmetric MCM (minichromosome maintenance) double hexamers is controversial, and importantly, it remains unknown when and how ORC proteins associate with the newly replicated origins to protect them from invasion by histones. Here, we report an essential and cell-cycle-dependent ORC "dimerization cycle" that plays three fundamental roles in the regulation of DNA replication: providing a symmetric platform to load the symmetric pre-RCs, marking and protecting the nascent sister replication origins for the next licensing, and playing a crucial role to prevent origin re-licensing within the same cell cycle.

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