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Phosphorylation of ORC2 Protein Dissociates Origin Recognition Complex from Chromatin and Replication Origins

机译:ORC2蛋白的磷酸化从染色质和复制起点分离出起点识别复合体。

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摘要

During the late M to the G1 phase of the cell cycle, the origin recognition complex (ORC) binds to the replication origin, leading to the assembly of the prereplicative complex for subsequent initiation of eukaryotic chromosome replication. We found that the cell cycle-dependent phosphorylation of human ORC2, one of the six subunits of ORC, dissociates ORC2, -3, -4, and -5 (ORC2–5) subunits from chromatin and replication origins. Phosphorylation at Thr-116 and Thr-226 of ORC2 occurs by cyclin-dependent kinase during the S phase and is maintained until the M phase. Phosphorylation of ORC2 at Thr-116 and Thr-226 dissociated the ORC2–5 from chromatin. Consistent with this, the phosphomimetic ORC2 protein exhibited defective binding to replication origins as well as to chromatin, whereas the phosphodefective protein persisted in binding throughout the cell cycle. These results suggest that the phosphorylation of ORC2 dissociates ORC from chromatin and replication origins and inhibits binding of ORC to newly replicated DNA.
机译:在细胞周期的M至G1晚期,起源识别复合物(ORC)与复制起点结合,从而导致复制前复合物的组装,随后启动真核染色体复制。我们发现,人类ORC2(ORC的六个亚基之一)的细胞周期依赖性磷酸化可从染色质和复制起点解离ORC2,-3,-4和-5(ORC2-5)亚基。 ORC2的Thr-116和Thr-226处的磷酸化由细胞周期蛋白依赖性激酶在S期发生,并一直维持到M期。在Thr-116和Thr-226处ORC2的磷酸化使ORC2-5与染色质解离。与此一致的是,拟磷酸化的ORC2蛋白与复制起点以及染色质的结合均表现出缺陷,而磷酸化缺陷蛋白则在整个细胞周期中都持续结合。这些结果表明,ORC2的磷酸化使ORC从染色质和复制起点解离,并抑制ORC与新复制的DNA结合。

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