The TEAD4-YAP/TAZ protein-protein interaction: expected similarities and unexpected differences

Chembiochem. 2013 Jul 8;14(10):1218-25. doi: 10.1002/cbic.201300163. Epub 2013 Jun 18.

Abstract

The Hippo pathway controls cell homeostasis, and its deregulation can lead to human diseases. In this pathway, the YAP and TAZ transcriptional cofactors play a key role in stimulating gene transcription through their interaction with the TEAD transcriptional factors. Our study of YAP and TAZ peptides in biochemical and biophysical assays shows that both proteins have essentially the same affinity for TEAD. Molecular modeling and structural biology data suggest that they also bind to the same site on TEAD. However, this apparent similarity hides differences in the ways in which the two proteins interact with TEAD. The secondary structure elements of their TEAD binding site do not contribute equally to the overall affinity, and critical interactions with TEAD are made through different residues. This convergent optimization of the YAP/TAZ TEAD binding site suggests that the similarity in the affinities of binding of YAP to TEAD and of TAZ to TEAD is important for Hippo pathway functionality.

Keywords: Hippo pathway; TAZ; TEAD; YAP; omega loops; peptides; protein-protein interactions.

MeSH terms

  • Acyltransferases
  • Amino Acid Sequence
  • Animals
  • DNA-Binding Proteins / chemistry
  • DNA-Binding Proteins / genetics
  • DNA-Binding Proteins / metabolism*
  • Hippo Signaling Pathway
  • Humans
  • Immunohistochemistry
  • Mice
  • Models, Molecular
  • Molecular Sequence Data
  • Muscle Proteins / chemistry
  • Muscle Proteins / genetics
  • Muscle Proteins / metabolism*
  • Mutagenesis, Site-Directed
  • Peptides / chemistry
  • Peptides / genetics
  • Peptides / metabolism
  • Protein Interaction Domains and Motifs
  • Protein Serine-Threonine Kinases / chemistry
  • Protein Serine-Threonine Kinases / genetics
  • Protein Serine-Threonine Kinases / metabolism*
  • Sequence Homology, Amino Acid
  • Signal Transduction
  • TEA Domain Transcription Factors
  • Transcription Factors / chemistry
  • Transcription Factors / genetics
  • Transcription Factors / metabolism*

Substances

  • DNA-Binding Proteins
  • Muscle Proteins
  • Peptides
  • TEA Domain Transcription Factors
  • TEAD4 protein, human
  • Transcription Factors
  • Acyltransferases
  • TAFAZZIN protein, human
  • Protein Serine-Threonine Kinases