The DNA damage response ( DDR) generates transient repair compartments to concentrate repair proteins and activate signaling factors. The physicochemical properties of these spatially confined compartments and their function remain poorly understood. Here, we establish, based on live cell microscopy and CRISPR/Cas9‐mediated endogenous protein tagging, that 53 BP1‐marked repair compartments are dynamic, show droplet‐like behavior, and undergo frequent fusion and fission events. 53 BP1 assembly, but not the upstream accumulation of γH2 AX and MDC1, is highly sensitive to changes in osmotic pressure, temperature, salt concentration and to disruption of hydrophobic interactions. Phase separation of 53 BP1 is substantiated by optoDroplet experiments, which further allowed dissection of the 53 BP1 sequence elements that cooperate for light‐induced clustering. Moreover, we found the tumor suppressor protein p53 to be enriched within 53 BP1 optoDroplets, and conditions that disrupt 53 BP1 phase separation impair 53 BP1‐dependent induction of p53 and diminish p53 target gene expression. We thus suggest that 53 BP1 phase separation integrates localized DNA damage recognition and repair factor assembly with global p53‐dependent gene activation and cell fate decisions.