DNA sequence encoded conformational flexibility orchestrates pioneer transcription factor nucleosome interaction landscape

Abstract

BackgroundEukaryotic gene regulation depends on transcription factors (TFs) recognizing short DNA motifs within chromatin. Many of these motifs lie within nucleosomes, where DNA is sharply bent, rotationally phased, and constrained by histone-DNA contacts. Yet only a subset is occupied in any cellular context. Motif identity alone, therefore, cannot fully explain selective TF engagement with nucleosomal DNA. We asked whether sequence-derived DNA conformational flexibility provides an interpretable representation of sequence context relevant to TF recognition on nucleosomes. ResultsWe compiled five DNA flexibility descriptors in the Python package DNAflexpy, representing bendability, torsional deformation, backbone conformational variability, and stiffness. We built quantitative models of TF binding affinity across 226 datasets from a high-throughput in vitro TF-nucleosome binding assay. Flexibility-augmented models improved prediction over mononucleotide baselines in most datasets, with smaller but reproducible gains over trinucleotide baselines. The gains were not uniform: they varied across TF families and were concordant with DNA shape-fluctuation features, suggesting that DNAflexpy descriptors capture a sequence-encoded structural signal. In PIONEAR-seq data, model performance generalized across nucleosomal templates in a TF- and sequence-dependent manner. Beyond prediction, position-resolved flexibility footprints revealed deformation signatures at cognate motifs and flanking regions across diverse TF families. For SOX11, model-derived footprints aligned with DNA shape fluctuations from nanosecond-to-microsecond molecular dynamics trajectories of SOX11-bound nucleosomes, consistent with independently observed DNA conformational dynamics and bound-state stabilization. The in vivo data showed a similar but more context-dependent pattern. OCT4 occupancy tended to correlate with local flexibility, whereas GATA3-pioneered regions showed flexibility coupled with altered rotational positioning of cognate motifs. Flexibility-augmented classifiers further improved discrimination of occupied nucleosomal motifs across ENCODE datasets. Torsional flexibility features, particularly twist dispersion and trx, were most informative for classification. ConclusionsSequence-derived DNA conformational flexibility provides a quantitative and interpretable representation of sequence context in TF recognition on nucleosomes. By augmenting sequence with structural information, these models help quantify and interpret an indirect-readout contribution in which DNA deformation tendencies may complement motif sequence and DNA shape. This framework may help explain why only selected motif instances are engaged in chromatin, without treating flexibility as independent of primary sequence.