NMR Spectroscopy, Bijvoet Center for Biomolecular Research, Utrecht University, Padualaan 8, 3584 CH Utrecht, the Netherlands.
NMR Spectroscopy, Bijvoet Center for Biomolecular Research, Utrecht University, Padualaan 8, 3584 CH Utrecht, the Netherlands.
J Mol Biol. 2021 Mar 19;433(6):166827. doi: 10.1016/j.jmb.2021.166827. Epub 2021 Jan 16.
The regulation of chromatin biology ultimately depends on the manipulation of its smallest subunit, the nucleosome. The proteins that bind and operate on the nucleosome do so, while their substrate is part of a polymer embedded in the dense nuclear environment. Their molecular interactions must in some way be tuned to deal with this complexity. Due to the rapid increase in the number of high-resolution structures of nucleosome-protein complexes and the increasing understanding of the cellular chromatin structure, it is starting to become clearer how chromatin factors operate in this complex environment. In this review, we analyze the current literature on the interplay between nucleosome-protein interactions and higher-order chromatin structure. We examine in what way nucleosomes-protein interactions can affect and can be affected by chromatin organization at the oligonucleosomal level. In addition, we review the characteristics of nucleosome-protein interactions that can cause phase separation of chromatin. Throughout, we hope to illustrate the exciting challenges in characterizing nucleosome-protein interactions beyond the nucleosome.
染色质生物学的调控最终取决于其最小亚基——核小体的操纵。结合并作用于核小体的蛋白质在其底物是嵌入在致密核环境中的聚合物的一部分时发挥作用。它们的分子相互作用必须以某种方式进行调整以应对这种复杂性。由于核小体-蛋白复合物的高分辨率结构数量的快速增加以及对细胞染色质结构的理解的增加,开始越来越清楚地了解染色质因子如何在这种复杂的环境中发挥作用。在这篇综述中,我们分析了关于核小体-蛋白相互作用与高级染色质结构相互作用的当前文献。我们研究了核小体-蛋白相互作用在什么程度上可以影响和可以被寡核小体水平的染色质组织所影响。此外,我们回顾了可以导致染色质相分离的核小体-蛋白相互作用的特征。总之,我们希望说明在核小体之外描述核小体-蛋白相互作用所面临的令人兴奋的挑战。