Leiden Institute of Chemistry, Leiden University, Einsteinweg 55, 2333CC Leiden, The Netherlands.
Biological and Soft Matter Physics, Huygens-Kamerlingh Onnes Laboratory, Leiden University, Niels Bohrweg 2, 2333CA Leiden, The Netherlands.
Nucleic Acids Res. 2021 May 7;49(8):4338-4349. doi: 10.1093/nar/gkaa1196.
Many archaea express histones, which organize the genome and play a key role in gene regulation. The structure and function of archaeal histone-DNA complexes remain however largely unclear. Recent studies show formation of hypernucleosomes consisting of DNA wrapped around an 'endless' histone-protein core. However, if and how such a hypernucleosome structure assembles on a long DNA substrate and which interactions provide for its stability, remains unclear. Here, we describe micromanipulation studies of complexes of the histones HMfA and HMfB with DNA. Our experiments show hypernucleosome assembly which results from cooperative binding of histones to DNA, facilitated by weak stacking interactions between neighboring histone dimers. Furthermore, rotational force spectroscopy demonstrates that the HMfB-DNA complex has a left-handed chirality, but that torque can drive it in a right-handed conformation. The structure of the hypernucleosome thus depends on stacking interactions, torque, and force. In vivo, such modulation of the archaeal hypernucleosome structure may play an important role in transcription regulation in response to environmental changes.
许多古菌表达组蛋白,组蛋白可组织基因组并在基因调控中发挥关键作用。然而,古菌组蛋白-DNA 复合物的结构和功能在很大程度上仍不清楚。最近的研究表明,由 DNA 缠绕在“无尽”组蛋白核心上形成超核小体。然而,这种超核小体结构是否以及如何在长 DNA 底物上组装,以及哪些相互作用提供其稳定性,仍不清楚。在这里,我们描述了 HMfA 和 HMfB 组蛋白与 DNA 复合物的微观操作研究。我们的实验表明,超核小体的组装是由组蛋白与 DNA 的协同结合引起的,这是由相邻组蛋白二聚体之间的弱堆积相互作用促进的。此外,旋转力谱学表明,HMfB-DNA 复合物具有左手手性,但扭矩可以驱动其形成右手构象。因此,超核小体的结构取决于堆积相互作用、扭矩和力。在体内,这种古菌超核小体结构的调节可能在转录调控中发挥重要作用,以响应环境变化。