DNA Damage-Induced Nuclear STING Translocation Orchestrates Innate Immune Activation and Chromatin Remodeling [ChIP-Seq]

To investigate the function of nuclear STING and its regulatory mechanisms, we treated wild-type (WT) HeLa cells with BMN673 for 24 hours to promote nuclear STING translocation. ChIP-seq was performed using HeLa cells treated with BMN673 for 24 hours. Overall design: ChIP-seq analysis of WT HeLa cells after 24 hours of BMN673 treatment to promote nuclear STING translocation.