| Literature DB >> 33723431 |
Sophia Z Shalhout1,2,3, Peng-Yu Yang4,5, Edyta M Grzelak4, Kayla Nutsch4, Sida Shao4, Claudio Zambaldo4, Jonathan Iaconelli4, Lara Ibrahim4, Caroline Stanton4, Stormi R Chadwick4, Emily Chen5, Michael DeRan6, Sijia Li5, Mitchell Hull5, Xu Wu6, Arnab K Chatterjee5, Weijun Shen7, Fernando D Camargo8,9,10, Peter G Schultz11,12, Michael J Bollong13.
Abstract
The transcriptional coactivator Yes-associated protein 1 (YAP) orchestrates a proproliferative transcriptional program that controls the fate of somatic stem cells and the regenerative responses of certain tissues. As such, agents that activate YAP may hold therapeutic potential in disease states exacerbated by insufficient proliferative repair. Here we report the discovery of a small molecule, termed PY-60, which robustly activates YAP transcriptional activity in vitro and promotes YAP-dependent expansion of epidermal keratinocytes in mouse following topical drug administration. Chemical proteomics revealed the relevant target of PY-60 to be annexin A2 (ANXA2), a protein that directly associates with YAP at the cell membrane in response to increased cell density. PY-60 treatment liberates ANXA2 from the membrane, ultimately promoting a phosphatase-bound, nonphosphorylated and transcriptionally active form of YAP. This work reveals ANXA2 as a previously undescribed, druggable component of the Hippo pathway and suggests a mechanistic rationale to promote regenerative repair in disease.Entities:
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Year: 2021 PMID: 33723431 DOI: 10.1038/s41589-021-00755-0
Source DB: PubMed Journal: Nat Chem Biol ISSN: 1552-4450 Impact factor: 15.040