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染色质化起始点通过相互作用和空间限制降低了 ORC 和 MCM 的流动性。

A chromatinized origin reduces the mobility of ORC and MCM through interactions and spatial constraint.

机构信息

Department of Bionanoscience, Kavli Institute of Nanoscience, Delft University of Technology, Delft, The Netherlands.

Chromosome Replication Laboratory, Francis Crick Institute, London, United Kingdom.

出版信息

Nat Commun. 2023 Oct 23;14(1):6735. doi: 10.1038/s41467-023-42524-8.

Abstract

Chromatin replication involves the assembly and activity of the replisome within the nucleosomal landscape. At the core of the replisome is the Mcm2-7 complex (MCM), which is loaded onto DNA after binding to the Origin Recognition Complex (ORC). In yeast, ORC is a dynamic protein that diffuses rapidly along DNA, unless halted by origin recognition sequences. However, less is known about the dynamics of ORC proteins in the presence of nucleosomes and attendant consequences for MCM loading. To address this, we harnessed an in vitro single-molecule approach to interrogate a chromatinized origin of replication. We find that ORC binds the origin of replication with similar efficiency independently of whether the origin is chromatinized, despite ORC mobility being reduced by the presence of nucleosomes. Recruitment of MCM also proceeds efficiently on a chromatinized origin, but subsequent movement of MCM away from the origin is severely constrained. These findings suggest that chromatinized origins in yeast are essential for the local retention of MCM, which may facilitate subsequent assembly of the replisome.

摘要

染色质复制涉及核小体景观内复制体的组装和活性。复制体的核心是 Mcm2-7 复合物(MCM),它在与起始识别复合物(ORC)结合后被加载到 DNA 上。在酵母中,ORC 是一种快速扩散的动态蛋白,除非被起始识别序列阻止。然而,关于 ORC 蛋白在核小体存在下的动力学及其对 MCM 加载的影响知之甚少。为了解决这个问题,我们利用一种体外单分子方法来研究染色质复制起始点。我们发现,ORC 结合复制起始点的效率相似,无论起始点是否被染色质化,尽管核小体的存在降低了 ORC 的流动性。MCM 的招募也能在染色质化的起始点上有效地进行,但随后 MCM 远离起始点的移动受到严重限制。这些发现表明,酵母中的染色质化起始点对于 MCM 的局部保留是必不可少的,这可能有助于随后复制体的组装。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a27/10593741/25e058b6b147/41467_2023_42524_Fig1_HTML.jpg

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