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Updated: Dec 13, 2025

Identification of Transcription Factor Regulators using Medium-Throughput Screening of Arrayed Libraries and a Dual-Luciferase-Based Reporter
Published on: March 27, 2020
An overview of signaling pathways regulating YAP/TAZ activity
Boon Chin Heng1,2, Xuehui Zhang3,4, Dominique Aubel5
1Central Laboratory, Peking University School and Hospital of Stomatology, Beijing, 100081, People's Republic of China.
Abstract:
YAP and TAZ are ubiquitously expressed homologous proteins originally identified as penultimate effectors of the Hippo signaling pathway, which plays a key role in maintaining mammalian tissue/organ size. Presently, it is known that YAP/TAZ also interact with various non-Hippo signaling pathways, and have diverse roles in multiple biological processes, including cell proliferation, tissue regeneration, cell lineage fate determination, tumorigenesis, and mechanosensing. In this review, we first examine the various microenvironmental cues and signaling pathways that regulate YAP/TAZ activation, through the Hippo and non-Hippo signaling pathways. This is followed by a brief summary of the interactions of YAP/TAZ with TEAD1-4 and a diverse array of other non-TEAD transcription factors. Finally, we offer a critical perspective on how increasing knowledge of the regulatory mechanisms of YAP/TAZ signaling might open the door to novel therapeutic applications in the interrelated fields of biomaterials, tissue engineering, regenerative medicine and synthetic biology.
Insights
The Hippo pathway effectors, YAP and TAZ, regulate tissue size and have roles in cell proliferation and regeneration. Understanding their signaling pathways offers potential therapeutic applications in regenerative medicine and biomaterials.
Area of Science:
- Cell Biology
- Biochemistry
- Regenerative Medicine
Background:
- YAP (Yes-associated protein) and TAZ (Transcriptional co-activator with PDZ-binding motif) are homologous proteins.
- They are key effectors of the Hippo signaling pathway, crucial for maintaining mammalian tissue and organ size.
- YAP/TAZ also participate in non-Hippo pathways, influencing cell proliferation, regeneration, lineage determination, tumorigenesis, and mechanosensing.
Purpose of the Study:
- To review microenvironmental cues and signaling pathways regulating YAP/TAZ activation via Hippo and non-Hippo pathways.
- To summarize YAP/TAZ interactions with TEAD transcription factors and other non-TEAD factors.
- To provide a perspective on therapeutic applications of YAP/TAZ signaling knowledge.
Main Methods:
- Literature review of YAP/TAZ signaling pathways.
- Analysis of YAP/TAZ interactions with transcription factors.
- Critical perspective on therapeutic potential.
Main Results:
- YAP/TAZ activation is modulated by diverse microenvironmental cues and signaling networks.
- YAP/TAZ interact with TEAD1-4 and numerous other transcription factors.
- Knowledge of YAP/TAZ regulation is expanding.
Conclusions:
- Understanding YAP/TAZ regulation is crucial for various biological processes.
- Further insights into YAP/TAZ signaling can drive innovation in biomaterials and tissue engineering.
- Therapeutic strategies targeting YAP/TAZ hold promise for regenerative medicine and synthetic biology.
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