Swiss Institute for Experimental Cancer Research (ISREC), EPFL, Lausanne 1015, Switzerland.
Friedrich Miescher Institute for Biomedical Research, Maulbeerstrasse 66, Basel 4058, Switzerland.
Curr Opin Struct Biol. 2024 Oct;88:102875. doi: 10.1016/j.sbi.2024.102875. Epub 2024 Jul 10.
Pioneering transcription factors (TFs) can drive cell fate changes by binding their DNA motifs in a repressive chromatin environment. Recent structures illustrate emerging rules for nucleosome engagement: TFs distort the nucleosomal DNA to gain access or employ alternative DNA-binding modes with smaller footprints, they preferentially access solvent-exposed motifs near the entry/exit sites, and frequently interact with histones. The extent of TF-histone interactions, in turn, depends on the motif location on the nucleosome, the type of DNA-binding fold, and adjacent domains present. TF-histone interactions can phase TF motifs relative to nucleosomes, and we discuss how these complex and surprisingly diverse interactions between nucleosomes and TFs contribute to function.
开创性的转录因子 (TFs) 可以通过在抑制性染色质环境中结合其 DNA 基序来驱动细胞命运的改变。最近的结构阐明了核小体结合的新兴规则:TFs 扭曲核小体 DNA 以获得进入或采用具有较小足迹的替代 DNA 结合模式,它们优先访问进入/退出位点附近暴露在溶剂中的基序,并且经常与组蛋白相互作用。TF-组蛋白相互作用的程度反过来又取决于核小体上的基序位置、DNA 结合折叠的类型以及存在的相邻结构域。TF-组蛋白相互作用可以使 TF 基序相对于核小体相位,我们讨论了核小体和 TFs 之间的这些复杂且令人惊讶的多样化相互作用如何促进功能。