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解析大肠杆菌中 DNA 复制和细胞分裂的控制机制。

Dissecting the Control Mechanisms for DNA Replication and Cell Division in E. coli.

机构信息

Department of Environmental Microbiology, Eawag, Dübendorf, Switzerland; Department of Environmental Systems Science, ETH Zürich, Zürich, Switzerland.

Santa Fe Institute, 1399 Hyde Park Road, Santa Fe, NM 87501, USA; The Abdus Salam International Centre for Theoretical Physics (ICTP), Strada Costiera 11, 34014 Trieste, Italy.

出版信息

Cell Rep. 2018 Oct 16;25(3):761-771.e4. doi: 10.1016/j.celrep.2018.09.061.

Abstract

Understanding the classic problem of how single E. coli cells coordinate cell division with genome replication would open the way to addressing cell-cycle progression at the single-cell level. Recent studies produced new data, but the contrast in their conclusions and proposed mechanisms makes the emerging picture fragmented and unclear. Here, we re-evaluate available data and models, including generalizations based on the same assumptions. We show that although they provide useful insights, none of the proposed models captures all correlation patterns observed in data. We conclude that the assumption that replication is the bottleneck process for cell division is too restrictive. Instead, we propose that two concurrent cycles responsible for division and initiation of DNA replication set the time of cell division. This framework allows us to select a nearly constant added size per origin between subsequent initiations as the most likely mechanism setting initiation of replication.

摘要

理解单个大肠杆菌细胞如何协调细胞分裂与基因组复制的经典问题,将为在单细胞水平上解决细胞周期进程问题开辟道路。最近的研究提供了新的数据,但它们的结论和提出的机制存在差异,使得新出现的图景变得零碎和不清楚。在这里,我们重新评估了现有的数据和模型,包括基于相同假设的推广。我们表明,尽管它们提供了有用的见解,但没有一个提出的模型能够捕捉到数据中观察到的所有相关模式。我们得出结论,认为复制是细胞分裂的瓶颈过程的假设过于局限。相反,我们提出,负责分裂和起始 DNA 复制的两个并发周期决定了细胞分裂的时间。这个框架允许我们选择下一次起始之间每个起始点的几乎恒定的附加大小作为最有可能的复制起始设置机制。

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