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A new class of disordered elements controls DNA replication through initiator self-assembly

机译:新型无序元素通过引发剂自组装控制DNA复制

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摘要

The initiation of DNA replication in metazoans occurs at thousands of chromosomal sites known as origins. At each origin, the Origin Recognition Complex (ORC), Cdc6, and Cdt1 co-assemble to load the Mcm2-7 replicative helicase onto chromatin. Current replication models envisage a linear arrangement of isolated origins functioning autonomously; the extent of inter-origin organization and communication is unknown. Here, we report that the replication initiation machinery of D. melanogaster unexpectedly undergoes liquid-liquid phase separation (LLPS) upon binding DNA in vitro. We find that ORC, Cdc6, and Cdt1 contain intrinsically disordered regions (IDRs) that drive LLPS and constitute a new class of phase separating elements. Initiator IDRs are shown to regulate multiple functions, including chromosome recruitment, initiator-specific co-assembly, and Mcm2-7 loading. These data help explain how CDK activity controls replication initiation and suggest that replication programs are subject to higher-order levels of inter-origin organization.
机译:后生动物中DNA复制的起始发生在成千上万个称为起源的染色体位点。在每个起点,起点识别复合体(ORC),Cdc6和Cdt1共同组装以将Mcm2-7复制解旋酶加载到染色质上。当前的复制模型设想了独立起作用的孤立起源的线性排列。产地组织和沟通的程度尚不清楚。在这里,我们报告说,D。melanogaster的复制启动机制意外地在体外结合DNA时经历了液-液相分离(LLPS)。我们发现ORC,Cdc6和Cdt1包含驱动LLPS并构成一类新的相分离元件的内在无序区(IDR)。引发剂IDR被证明可以调节多种功能,包括染色体募集,引发剂特异性共组装和Mcm2-7装载。这些数据有助于说明CDK活动如何控制复制的启动,并建议复制程序要受制于更高级别的域间组织。

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