University of Michigan, Ann Arbor, MI 48109, United States.
University of Michigan, Ann Arbor, MI 48109, United States; University of Wisconsin, Madison, WI 53706, United States.
Curr Opin Microbiol. 2018 Jun;43:38-45. doi: 10.1016/j.mib.2017.11.009. Epub 2017 Dec 1.
Although DNA replication and repair in bacteria have been extensively studied for many decades, in recent years the development of single-molecule microscopy has provided a new perspective on these fundamental processes. Because single-molecule imaging super-resolves the nanometer-scale dynamics of molecules, and because single-molecule imaging is sensitive to heterogeneities within a sample, this nanoscopic microscopy technique measures the motions, localizations, and interactions of proteins in real time without averaging ensemble observations, both in vitro and in vivo. In this Review, we provide an overview of several recent single-molecule fluorescence microscopy studies on DNA replication and repair. These experiments have shown that, in both Escherichia coli and Bacillus subtilis the DNA replication proteins are highly dynamic. In particular, even highly processive replicative DNA polymerases exchange to and from the replication fork on the scale of a few seconds. Furthermore, single-molecule investigations of the DNA mismatch repair (MMR) pathway have measured the complex interactions between MMR proteins, replication proteins, and DNA. Single-molecule imaging will continue to improve our understanding of fundamental processes in bacteria including DNA replication and repair.
尽管 DNA 复制和修复在细菌中已经被广泛研究了几十年,但近年来,单分子显微镜技术的发展为这些基本过程提供了新的视角。由于单分子成像可以超分辨分子的纳米级动力学,并且单分子成像对样品内的异质性敏感,因此这种纳米级显微镜技术可以实时测量蛋白质的运动、定位和相互作用,而无需对体外和体内的整体观察进行平均。在这篇综述中,我们概述了最近几项关于 DNA 复制和修复的单分子荧光显微镜研究。这些实验表明,在大肠杆菌和枯草芽孢杆菌中,DNA 复制蛋白都是高度动态的。特别是,即使是高度连续的复制 DNA 聚合酶也会在几秒钟的时间尺度上从复制叉上交换到复制叉上。此外,对 DNA 错配修复 (MMR) 途径的单分子研究已经测量了 MMR 蛋白、复制蛋白和 DNA 之间的复杂相互作用。单分子成像将继续提高我们对细菌中包括 DNA 复制和修复在内的基本过程的理解。