Affiliations 

  • 1 Central Laboratory, Peking University School and Hospital of Stomatology, Beijing, 100081, People's Republic of China
  • 2 Department of Dental Materials & Dental Medical Devices Testing Center, Peking University School and Hospital of Stomatology, Beijing, 100081, People's Republic of China
  • 3 IUTA, Departement Genie Biologique, Universite, Claude Bernard Lyon 1, Villeurbanne Cedex, France
  • 4 Department of Geriatric Dentistry, Peking University School and Hospital of Stomatology, Beijing, 100081, People's Republic of China
  • 5 Department of Biosystems Science and Engineering, ETH-Zurich, Mattenstrasse 26, Basel, 4058, Switzerland. martin.fussenegger@bsse.ethz.ch
  • 6 Department of Geriatric Dentistry, Peking University School and Hospital of Stomatology, Beijing, 100081, People's Republic of China. kqdengxuliang@bjmu.edu.cn
Cell Mol Life Sci, 2021 Jan;78(2):497-512.
PMID: 32748155 DOI: 10.1007/s00018-020-03579-8

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.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.