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体内酵母复制起点处复合物组装的两个步骤。

Two steps in the assembly of complexes at yeast replication origins in vivo.

作者信息

Diffley J F, Cocker J H, Dowell S J, Rowley A

机构信息

Imperial Cancer Research Fund, Clare Hall Laboratories, South Mimms, Hertfordshire, England.

出版信息

Cell. 1994 Jul 29;78(2):303-16. doi: 10.1016/0092-8674(94)90299-2.

Abstract

The integration of chromosomal DNA replication into the eukaryotic cell cycle might involve temporal regulation of interactions between cellular factors and replication origins. We show here that yeast replication origins exist in two chromatin states during the cell cycle. In the postreplicative state, genomic footprints closely resemble those produced in vitro by the purified ORC and ABF1 proteins, indicating that the binding of these proteins to replication origins is not sufficient to drive the initiation of DNA replication. The prereplicative state is characterized by an additional region of protection overlapping the ORC footprint. This prereplicative complex appears near the end of mitosis and persists through G1. After entry into S phase, origins return to the postreplicative state. Similarities in temporal regulation of the prereplicative state and the Xenopus licensing factor suggest that mechanisms limiting DNA replication to once per cell cycle may be conserved among eukaryotes.

摘要

染色体DNA复制与真核细胞周期的整合可能涉及细胞因子与复制起点之间相互作用的时间调控。我们在此表明,酵母复制起点在细胞周期中存在两种染色质状态。在复制后状态下,基因组足迹与纯化的ORC和ABF1蛋白在体外产生的足迹非常相似,这表明这些蛋白与复制起点的结合不足以驱动DNA复制的起始。复制前状态的特征是存在一个与ORC足迹重叠的额外保护区域。这种复制前复合物在有丝分裂末期附近出现,并持续存在于G1期。进入S期后,起点恢复到复制后状态。复制前状态与非洲爪蟾许可因子在时间调控上的相似性表明,将DNA复制限制在每个细胞周期一次的机制可能在真核生物中是保守的。

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