ArticleBriefings in bioinformatics2026
TF-loop: deciphering the transcription factor regulatory language for CTCF-mediated chromatin loop based on BERT.
Article in Briefings in bioinformatics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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9 authors.
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Abstract
Chromatin looping, which facilitates the three-dimensional (3D) organization of the genome, is essential for the regulation of gene expression. This process relies on the interaction of numerous transcription factors (TFs), particularly CCCTC-binding factor (CTCF) and Cohesin, whose dynamic binding patterns orchestrate loop formation. Current computational methods for prediction of CTCF-mediated chromatin loops struggle to perform genome-wide predictions, primarily due to the extreme imbalance between positive and negative samples in training datasets. Existing DNA-sequence-based models often fail to capture the complex dynamics of TF binding and the regulatory code behind chromatin looping. To address these challenges, we present TF-loop, a novel TF regulatory language framework designed to predict chromatin loops. This framework conceptualizes TF sequences, defined by the binding positions and orientations of five key TFs, as a structured "TF language." Using the BERT model, TF-loop decodes the latent linguistic patterns embedded in these sequences, facilitating accurate predictions of chromatin loops. Comparative analysis with state-of-the-art model demonstrates that TF-loop significantly improves prediction accuracy across diverse cell types, even when faced with highly imbalanced datasets. The results highlight the potential of TF-loop to offer a new perspective on decoding the 3D structure of chromatin using natural language processing techniques.
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