Cis-Regulation of the CFTR Gene in Pancreatic Cells

Genome organization is essential for precise spatial and temporal gene expression and relies on interactions between promoters and distal <i>cis</i>-regulatory elements (CREs), which constitute ~8% of the human genome. For the <i>cystic fibrosis transmembrane conductance regulator</i> (<i>CFTR</i>) gene, tissue-specific expression, especially in the pancreas, remains poorly understood. Unraveling its regulation could clarify the clinical heterogeneity observed in cystic fibrosis and CFTR-related disorders. To understand the role of 3D chromatin architecture in establishing tissue-specific expression of the <i>CFTR</i> gene, we mapped chromatin interactions and epigenomic regulation in Capan-1 pancreatic cells. Candidate CREs are validated by luciferase reporter assay and CRISPR knock-out. We identified active CREs not only around the <i>CFTR</i> gene but also outside the topologically associating domain (TAD). We demonstrate the involvement of multiple CREs upstream and downstream of the <i>CFTR</i> gene and reveal a cooperative effect of the -44 kb, -35 kb, +15.6 kb, and +37.7 kb regions, which share common predicted transcription factor (TF) motifs. We also extend our analysis to compare 3D chromatin conformation in intestinal and pancreatic cells, providing valuable insights into the tissue specificity of CREs in regulating <i>CFTR</i> gene expression.