Palmitoylation of TEAD Transcription Factors Is Required for Their Stability and Function in Hippo Pathway Signaling

Structure. 2016 Jan 5;24(1):179-186. doi: 10.1016/j.str.2015.11.005. Epub 2015 Dec 24.

Abstract

The Hippo signaling pathway is responsible for regulating the function of TEAD family transcription factors in metazoans. TEADs, with their co-activators YAP/TAZ, are critical for controlling cell differentiation and organ size through their transcriptional activation of genes involved in cell growth and proliferation. Dysregulation of the Hippo pathway has been implicated in multiple forms of cancer. Here, we identify a novel form of regulation of TEAD family proteins. We show that human TEADs are palmitoylated at a universally conserved cysteine, and report the crystal structures of the human TEAD2 and TEAD3 YAP-binding domains in their palmitoylated forms. These structures show a palmitate bound within a highly conserved hydrophobic cavity at each protein's core. Our findings also demonstrate that this modification is required for proper TEAD folding and stability, indicating a potential new avenue for pharmacologically regulating the Hippo pathway through the modulation of TEAD palmitoylation.

MeSH terms

  • Adaptor Proteins, Signal Transducing / metabolism
  • Amino Acid Sequence
  • Cysteine / metabolism
  • DNA-Binding Proteins / chemistry*
  • DNA-Binding Proteins / metabolism
  • HeLa Cells
  • Hippo Signaling Pathway
  • Humans
  • Lipoylation
  • Molecular Sequence Data
  • Nuclear Envelope / metabolism
  • Phosphoproteins / metabolism
  • Protein Binding
  • Protein Folding
  • Protein Processing, Post-Translational*
  • Protein Serine-Threonine Kinases / metabolism*
  • Protein Stability
  • Signal Transduction*
  • TEA Domain Transcription Factors
  • Transcription Factors / chemistry*
  • Transcription Factors / metabolism
  • YAP-Signaling Proteins

Substances

  • Adaptor Proteins, Signal Transducing
  • DNA-Binding Proteins
  • Phosphoproteins
  • TEA Domain Transcription Factors
  • TEAD2 protein, human
  • TEAD3 protein, human
  • Transcription Factors
  • YAP-Signaling Proteins
  • YAP1 protein, human
  • Protein Serine-Threonine Kinases
  • Cysteine