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Palmitoylation of TEAD Transcription Factors Is Required for Their Stability and Function in Hippo Pathway Signaling
- Source :
- Structure. 24(1):179-186
- Publication Year :
- 2016
- Publisher :
- Elsevier BV, 2016.
-
Abstract
- SummaryThe 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.
- Subjects :
- 0301 basic medicine
Protein Folding
Nuclear Envelope
Lipoylation
Cellular differentiation
Molecular Sequence Data
Protein Serine-Threonine Kinases
Biology
03 medical and health sciences
Palmitoylation
Transcription (biology)
Structural Biology
Humans
Hippo Signaling Pathway
Amino Acid Sequence
Cysteine
TEAD3
TEAD2
Gene
Transcription factor
Molecular Biology
Adaptor Proteins, Signal Transducing
Hippo signaling pathway
Protein Stability
TEA Domain Transcription Factors
YAP-Signaling Proteins
Phosphoproteins
Cell biology
DNA-Binding Proteins
030104 developmental biology
Protein Processing, Post-Translational
HeLa Cells
Protein Binding
Signal Transduction
Transcription Factors
Subjects
Details
- ISSN :
- 09692126
- Volume :
- 24
- Issue :
- 1
- Database :
- OpenAIRE
- Journal :
- Structure
- Accession number :
- edsair.doi.dedup.....89d9313f2c57a968a068717e592b2122
- Full Text :
- https://doi.org/10.1016/j.str.2015.11.005