Todolli Stefjord, Nizovtseva Ekaterina V, Clauvelin Nicolas, Maxian Ondrej, Studitsky Vasily M, Olson Wilma K
Department of Chemistry and Chemical Biology, Center for Quantitative Biology, Rutgers, The State University of New Jersey, 610 Taylor Road, Piscataway, New Jersey 08854, USA.
Cancer Epigenetics Program, Fox Chase Cancer Center, 333 Cottman Avenue, Philadelphia, Pennsylvania 19422, USA.
J Chem Phys. 2024 Dec 28;161(24). doi: 10.1063/5.0240991.
The dynamic organization of chromatin plays an essential role in the regulation of genetic activity, interconverting between open and compact forms at the global level. The mechanisms underlying these large-scale changes remain a topic of widespread interest. The simulations of nucleosome-decorated DNA reported herein reveal profound effects of the nucleosome itself on overall chromatin properties. Models that capture the long-range communication between proteins on nucleosome-decorated DNA chains incorporate DNA pathways different from those that were previously proposed based on ultracentrifugation and chemical cross-linking data. New quantitative biochemical assays measuring the rates of communication between interacting proteins bound to a promoter and an enhancer at the ends of saturated, precisely positioned, nucleosome-decorated DNA chains reveal a chromatin architecture with a three-nucleosome repeat, a model inconsistent with the two-start configurations deduced from earlier physical studies. Accompanying computations uncover small differences in the twisting of successive base pairs that seemingly give rise to the observed global properties. These data suggest that the novel state of chromatin determined under physiological conditions differs from that deduced under standard physical conditions, likely reflecting the different salt conditions used in the two types of experiments. This novel chromatin state may be important for a number of DNA transactions that occur in the cell nucleus.
染色质的动态组织在基因活性调控中起着至关重要的作用,在全局水平上在开放和紧密形式之间相互转换。这些大规模变化背后的机制仍然是广泛关注的话题。本文报道的核小体修饰DNA的模拟揭示了核小体本身对整体染色质特性的深远影响。捕捉核小体修饰DNA链上蛋白质之间远程通讯的模型纳入了与先前基于超速离心和化学交联数据提出的不同的DNA途径。新的定量生化分析测量了结合在饱和、精确定位的核小体修饰DNA链末端的启动子和增强子上相互作用蛋白质之间的通讯速率,揭示了一种具有三个核小体重复的染色质结构,这一模型与早期物理研究推断的双起始构型不一致。伴随的计算揭示了连续碱基对扭曲的微小差异,这些差异似乎导致了观察到的全局特性。这些数据表明,在生理条件下确定的染色质新状态不同于在标准物理条件下推断的状态,这可能反映了两种类型实验中使用的不同盐条件。这种新的染色质状态可能对细胞核中发生的许多DNA交易很重要。