DNA binding partners of YAP/TAZ

BMB Rep. 2018 Mar;51(3):126-133. doi: 10.5483/bmbrep.2018.51.3.015.

Abstract

Hippo signaling plays critical roles in regulation of tissue homeostasis, organ size, and tumorigenesis by inhibiting YES-associated protein (YAP) and PDZ-binding protein TAZ through MST1/2 and LATS1/2 pathway. It is also engaged in cross-talk with various other signaling pathways, including WNT, BMPs, Notch, GPCRs, and Hedgehog to further modulate activities of YAP/TAZ. Because YAP and TAZ are transcriptional coactivators that lack DNA-binding activity, both proteins must interact with DNA-binding transcription factors to regulate target gene's expression. To activate target genes involved in cell proliferation, TEAD family members are major DNA-binding partners of YAP/TAZ. Accordingly, YAP/TAZ were originally classified as oncogenes. However, YAP might also play tumor-suppressing role. For example, YAP can bind to DNA-binding tumor suppressors including RUNXs and p73. Thus, YAP might act either as an oncogene or tumor suppressor depending on its binding partners. Here, we summarize roles of YAP depending on its DNA-binding partners and discuss context-dependent functions of YAP/TAZ. [BMB Reports 2018; 51(3): 126-133].

Publication types

  • Review

MeSH terms

  • Acyltransferases
  • Animals
  • Cell Cycle Proteins
  • Core Binding Factor alpha Subunits / metabolism
  • Hepatocyte Growth Factor / metabolism
  • Humans
  • Nuclear Proteins / metabolism
  • Protein Serine-Threonine Kinases / metabolism
  • Proto-Oncogene Proteins / metabolism
  • Serine-Threonine Kinase 3
  • Signal Transduction / physiology
  • Transcription Factors / metabolism*
  • Tumor Suppressor Proteins / metabolism

Substances

  • Cell Cycle Proteins
  • Core Binding Factor alpha Subunits
  • Nuclear Proteins
  • Proto-Oncogene Proteins
  • Transcription Factors
  • Tumor Suppressor Proteins
  • YY1AP1 protein, human
  • macrophage stimulating protein
  • Hepatocyte Growth Factor
  • Acyltransferases
  • TAFAZZIN protein, human
  • LATS1 protein, human
  • LATS2 protein, human
  • Protein Serine-Threonine Kinases
  • STK3 protein, human
  • Serine-Threonine Kinase 3