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移动起始因子赋予对 RNA 聚合酶冲突的抗性。

Mobile origin-licensing factors confer resistance to conflicts with RNA polymerase.

机构信息

Structure and Dynamics of Molecular Machines, Max Planck Institute of Biochemistry, Am Klopferspitz 18, 82152 Martinsried, Germany.

Memorial Sloan Kettering Cancer Center, Molecular Biology Program, 1275 York Avenue, New York, NY 10065, USA.

出版信息

Cell Rep. 2022 Mar 22;38(12):110531. doi: 10.1016/j.celrep.2022.110531.

Abstract

Fundamental to our understanding of chromosome duplication is the idea that replication origins function both as sites where MCM helicases are loaded during the G1 phase and where synthesis begins in S phase. However, the temporal delay between phases exposes the replisome assembly pathway to potential disruption prior to replication. Using multicolor, single-molecule imaging, we systematically study the consequences of encounters between actively transcribing RNA polymerases (RNAPs) and replication initiation intermediates in the context of chromatin. We demonstrate that RNAP can push multiple licensed MCM helicases over long distances with nucleosomes ejected or displaced. Unexpectedly, we observe that MCM helicase loading intermediates also can be repositioned by RNAP and continue origin licensing after encounters with RNAP, providing a web of alternative origin specification pathways. Taken together, our observations reveal a surprising mobility in origin-licensing factors that confers resistance to the complex challenges posed by diverse obstacles encountered on chromosomes.

摘要

我们对染色体复制的基本理解是,复制起点的作用既是在 G1 期加载 MCM 解旋酶的位点,也是在 S 期开始合成的位点。然而,在两个阶段之间的时间延迟会使复制前的复制体组装途径面临潜在的破坏。我们使用多色、单分子成像技术,在染色质背景下系统地研究了活跃转录的 RNA 聚合酶 (RNAP) 与复制起始中间体之间相遇的后果。我们证明,RNAP 可以在核小体被弹出或移位的情况下,将多个许可的 MCM 解旋酶推过很长的距离。出乎意料的是,我们观察到 MCM 解旋酶加载中间体也可以被 RNAP 重新定位,并在与 RNAP 相遇后继续进行起始许可,提供了一个替代起始指定途径的网络。总之,我们的观察结果揭示了起始许可因子令人惊讶的流动性,这使其能够抵抗染色体上遇到的各种障碍所带来的复杂挑战。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4775/8961423/be1777bce7e9/fx1.jpg

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