Mechanistic dissection of GRHL2 and PR transcriptional co-regulation in breast cells

This dataset belongs to a study in which we functionally dissect the transcriptional co-regulation by grainyhead-like 2 (GRHL2) and progesterone receptor (PR, also referred to as PGR) in human breast cancer cells. As part of these efforts, we performed CUT&RUN in T47DS for endogenous GRHL2 and PR. Gene expression is controlled by complex transcriptional networks in which transcription factors and their cognate enhancer elements integrate developmental and environmental cues. The progesterone receptor (PR), a hormone-activated transcription factor, is essential for breast development and physiology, yet how it engages with the chromatin and lineage-specific cofactors remains unclear. Using an unbiased approach, we identify the epithelial transcription factor grainyhead-like 2 (GRHL2) as a key co-regulator of PR activity in hormone responsive breast cancer cells. We show that GRHL2 interacts with PR in a progesterone-independent manner. Upon progesterone stimulation, GRHL2 and PR are both recruited to distal enhancer elements. Furthermore, GRHL2- and PR-bound elements connect spatially through chromatin looping to regulate shared targets. These findings uncover a previously unrecognized mechanism by which GRHL2 and PR coordinate gene regulation through both chromatin binding and 3D genome architecture modification, positioning GRHL2 as a crucial modulator of steroid hormone receptor function. CUT&RUN for PR, GRHL2 and IgG in T47DS cells either non-treated or 1nM R5020 treated for 4 hours.