Identification of Quinolinols as Activators of TEAD-Dependent Transcription
Author(s) -
Ajaybabu V. Pobbati,
Tom Mejuch,
Sayan Chakraborty,
Hacer Karataş,
S.R. Bharath,
Stéphanie M. Guéret,
Pierre-Alexis Goy,
G. Hahne,
Axel Pahl,
Sonja Sievers,
Ernesto Guccione,
Haiwei Song,
Herbert Waldmann,
Wanjin Hong
Publication year - 2019
Publication title -
acs chemical biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.899
H-Index - 111
eISSN - 1554-8937
pISSN - 1554-8929
DOI - 10.1021/acschembio.9b00786
Subject(s) - identification (biology) , transcription (linguistics) , computational biology , transcription factor , biology , computer science , genetics , gene , ecology , philosophy , linguistics
The transcriptional co-regulators YAP (Yes-associated protein) and TAZ (transcriptional coactivator with PDZ-binding motif) are the vertebrate downstream effectors of the Hippo signaling pathway that controls various physiological and pathological processes. YAP and TAZ pair with the TEAD (TEA domain) family of transcription factors to initiate transcription. We previously identified a tractable pocket in TEADs, which has been physiologically shown to bind palmitate. Herein, a TEAD-palmitate interaction screen was developed to select small molecules occupying the palmitate-binding pocket (PBP) of TEADs. We show that quinolinols were TEAD-binding compounds that augment YAP/TAZ-TEAD activity, which was verified using TEAD reporter assay, RT-qPCR, and RNA-Seq analyses. Structure-activity relationship investigations uncovered the quinolinol substituents that are necessary for TEAD activation. We reveal a novel mechanism where quinolinols stabilize YAP/TAZ protein levels by occupying the PBP. The enhancement of YAP activity by quinolinols accelerates the in vivo wound closure in a mouse wound-healing model. Although small molecules that occupy the PBP have been shown to inhibit YAP/TAZ-TEAD activity, leveraging PBP to activate TEADs is a novel approach.
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