Basic Sciences Division, Fred Hutchinson Cancer Center, Seattle, WA, USA.
University of Nebraska Medical Center, Department of Genetics, Cell Biology & Anatomy, Omaha, NE, USA.
Mol Cell. 2024 Jan 18;84(2):194-201. doi: 10.1016/j.molcel.2023.10.045. Epub 2023 Nov 27.
In eukaryotic genomes, transcriptional machinery and nucleosomes compete for binding to DNA sequences; thus, a crucial aspect of gene regulatory element function is to modulate chromatin accessibility for transcription factor (TF) and RNA polymerase binding. Recent structural studies have revealed multiple modes of TF engagement with nucleosomes, but how initial "pioneering" results in steady-state DNA accessibility for further TF binding and RNA polymerase II (RNAPII) engagement has been unclear. Even less well understood is how distant sites of open chromatin interact with one another, such as when developmental enhancers activate promoters to release RNAPII for productive elongation. Here, we review evidence for the centrality of the conserved SWI/SNF family of nucleosome remodeling complexes, both in pioneering and in mediating enhancer-promoter contacts. Consideration of the nucleosome unwrapping and ATP hydrolysis activities of SWI/SNF complexes, together with their architectural features, may reconcile steady-state TF occupancy with rapid TF dynamics observed by live imaging.
在真核基因组中,转录机制和核小体竞争与 DNA 序列结合;因此,基因调控元件功能的一个关键方面是调节转录因子 (TF) 和 RNA 聚合酶 (RNAPII) 结合的染色质可及性。最近的结构研究揭示了 TF 与核小体结合的多种模式,但最初“开拓性”如何导致稳定状态的 DNA 可及性以进一步结合 TF 和 RNA 聚合酶 II (RNAPII) 仍不清楚。更不清楚的是,开放染色质的远程位点如何相互作用,例如发育增强子如何激活启动子以释放 RNAPII 进行有效的延伸。在这里,我们回顾了保守的 SWI/SNF 家族核小体重塑复合物在开拓性和介导增强子-启动子接触中的核心作用的证据。考虑到 SWI/SNF 复合物的核小体解缠绕和 ATP 水解活性,以及它们的结构特征,可能会将稳态 TF 占有率与活细胞成像观察到的快速 TF 动力学协调起来。