Ashwin S S, Maeshima Kazuhiro, Sasai Masaki
Department of Applied Physics, Nagoya University, Nagoya, 464-8603, Japan.
National Institute of Genetics, Mishima, Shizuoka, 411-8540, Japan.
Biophys Rev. 2020 Apr;12(2):461-468. doi: 10.1007/s12551-020-00675-8. Epub 2020 Mar 23.
Eukaryotic chromatin is a complex of genome DNA and associated proteins, and its structure and dynamics play a crucial role in regulating DNA functions. Chromatin takes rather irregular structures in the nucleus and exhibits heterogeneous sub-diffusive movements as polymers fluctuating in a fluid state. Using genome-wide single-nucleosome tracking data, heterogeneity of movements was statistically analyzed, which categorized chromatin into two types: slow chromatin that moves under structurally constrained environments and fast chromatin that moves with less constraints. Interactions of chromatin to various protein factors determine the motional constraints. For example, loss of the cohesin complex that bundles the chromatin chains reduces the motional constraints and increases the population of fast chromatin. Another example is the transcriptional machinery. While it was previously thought that the transcriptional activity is associated with more open and dynamic chromatin structure, recent studies suggested a more nuanced role of transcription in chromatin dynamics: dynamic association/dissociation of active RNA polymerase II (RNAPII) and other transcription factors and Mediators (TF-Meds) transiently bridges transcriptionally active DNA regions, which forms a loose network of chromatin and constrains chromatin movement, enhancing the slow chromatin population. This new view on the dynamical effects of transcription urges a reflection on the traditional model of transcription factories and invites the more recent models of condensates/phase-separated liquid droplets of RNAPII, transcription factors, and Mediators. The combined procedure of genome-wide single-nucleosome tracking and its statistical analysis would unveil heterogeneity in the chromatin movement, which should provide a key to understanding the relations among chromatin dynamics, structure, and function.
真核染色质是基因组DNA与相关蛋白质的复合物,其结构和动态变化在调节DNA功能中起着至关重要的作用。染色质在细胞核中呈现出相当不规则的结构,并表现出异质性的亚扩散运动,就像聚合物在流体状态下波动一样。利用全基因组单核小体追踪数据,对运动的异质性进行了统计分析,将染色质分为两类:在结构受限环境下移动的慢染色质和移动受限较少的快染色质。染色质与各种蛋白质因子的相互作用决定了运动约束。例如,捆绑染色质链的黏连蛋白复合物的缺失会减少运动约束,并增加快染色质的比例。另一个例子是转录机制。虽然以前认为转录活性与更开放和动态的染色质结构有关,但最近的研究表明转录在染色质动态变化中起着更微妙的作用:活性RNA聚合酶II(RNAPII)和其他转录因子及中介体(TF-Meds)的动态结合/解离短暂地连接转录活跃的DNA区域,形成一个松散的染色质网络并限制染色质运动,增加慢染色质的比例。这种关于转录动态效应的新观点促使人们反思传统的转录工厂模型,并引出了关于RNAPII、转录因子和中介体的凝聚物/相分离液滴的更新模型。全基因组单核小体追踪及其统计分析的联合程序将揭示染色质运动中的异质性,这应该为理解染色质动态变化、结构和功能之间的关系提供关键线索。