Chanou Anna, Hamperl Stephan
Chromosome Dynamics and Genome Stability, Institute of Epigenetics and Stem Cells, Helmholtz Zentrum München, Munich, Germany.
Front Cell Dev Biol. 2021 Jul 5;9:699771. doi: 10.3389/fcell.2021.699771. eCollection 2021.
Besides the basic organization in nucleosome core particles (NCPs), eukaryotic chromatin is further packed through interactions with numerous protein complexes including transcription factors, chromatin remodeling and modifying enzymes. This nucleoprotein complex provides the template for many important biological processes, such as DNA replication, transcription, and DNA repair. Thus, to understand the molecular basis of these DNA transactions, it is critical to define individual changes of the chromatin structure at precise genomic regions where these machineries assemble and drive biological reactions. Single-molecule approaches provide the only possible solution to overcome the heterogenous nature of chromatin and monitor the behavior of individual chromatin transactions in real-time. In this review, we will give an overview of currently available single-molecule methods to obtain mechanistic insights into nucleosome positioning, histone modifications and DNA replication and transcription analysis-previously unattainable with population-based assays.
除了核小体核心颗粒(NCPs)中的基本组织形式外,真核染色质还通过与众多蛋白质复合物相互作用进一步组装,这些蛋白质复合物包括转录因子、染色质重塑和修饰酶。这种核蛋白复合物为许多重要的生物学过程提供模板,如DNA复制、转录和DNA修复。因此,为了理解这些DNA交易的分子基础,在这些机制组装并驱动生物反应的精确基因组区域定义染色质结构的个体变化至关重要。单分子方法是克服染色质异质性并实时监测单个染色质交易行为的唯一可行解决方案。在本综述中,我们将概述当前可用的单分子方法,以深入了解核小体定位、组蛋白修饰以及DNA复制和转录分析——这些是基于群体的检测方法以前无法实现的。