Résumé
Chromatin looping between cis-regulatory elements is essential for precise developmental gene expression, and its disruption is frequently linked to disease. Polycomb response elements (PREs) are specialized tethering elements that mediate chromatin loops and are bound by transcription factors (TFs) like GAGA-associated factor (GAF), contributing to the recruitment of Polycomb group (PcG) proteins. While both PcG proteins and GAF have been implicated in looping, their specific roles and the mechanisms of loop specificity remain unresolved. Using genomewide and locus-specific approaches, we show that high GAF occupancy is required for chromatin looping and gene regulation. However, GAF alone cannot establish loops without additional factors. Surprisingly, PRE looping does not require Polycomb repressive complex 1 (PRC1) or the repressive histone mark H3K27me3. Intriguingly, orthologous PRE sequences can rescue looping, while unrelated PREs with similar GAF levels cannot, indicating that looping specificity depends on both GAF levels and compatible factor combinations at loop anchors. Together, our results support a combinatorial model in which GAF collaborates with additional looping factors to drive PRE-specific interactions, suggesting that certain combinations of factors at PREs may determine which elements form loops and contribute to Polycomb-mediated gene silencing.