Mechanics-dependent Global Nuclear Eviction and Site-Specific Recruitment of YAP Regulates DNA Damage Responses

Yes-associated protein (YAP), a transcriptional coactivator, plays key roles in cell growth, proliferation and apoptosis, and its levels are frequently dysregulated in cancers. YAP levels in the nucleus are highly sensitive to nuclear mechanical cues, and such cues are also parallelly emerging to be a key modulator of DNA Damage Responses (DDR). However, whether DNA- damage can induce mechanical changes that regulate downstream events such as YAP localization and that in turn feeds back onto DDR activation, remains unknown. In this study, we report that YAP translocates in a nuclear mechanics-dependent manner upon induction of Double Strand Breaks (DSBs). This translocation is not a mere epiphenomenon, and we find that: first, global nuclear eviction of YAP enhances DDR signaling; second, local enrichment of YAP at DNA damage sites promotes recruitment of DNA repair proteins previously identified as potential interactors of YAP or its partner TEAD1. Together, these findings indicate that YAP is not only a transcriptional coactivator, but also plays an under-appreciated role in regulating DDR.