Snapshots of a hybrid transcription factor in the Hippo pathway

Research output: Contribution to journalReview article

10 Scopus citations

Abstract

The Hippo pathway plays key roles in animal development. It suppresses tumorigenesis by controlling the transcription of the target genes that are critical for cell proliferation and apoptosis. The transcriptional coactivator YAP is the major downstream effector of the Hippo signaling. Upon extracellular stimulation, a kinase cascade in the Hippo pathway phosphorylates YAP and promotes its cytoplasmic sequestration by 14-3-3 and ubiquitin-dependent degradation. When the Hippo pathway is turned off, YAP (which lacks a DNA-binding domain) is dephosphorylated and translocates to the nucleus, where it associates with the transcription factor TEAD to form a functional heterodimeric transcription factor and to promote the expression of the Hippo-responsive genes. Recently, structures of the YAP-binding domain of TEAD alone or in complex with YAP have revealed the atomic details of the TEAD-YAP interaction. Here, I review these exciting advances, propose a strategy for targeting the TEAD-YAP interaction using small molecules, and suggest potential mechanisms by which phosphorylation and 14-3-3 binding regulate the cytoplasmic retention of YAP.

Original languageEnglish (US)
Pages (from-to)811-819
Number of pages9
JournalProtein and Cell
Volume1
Issue number9
DOIs
StatePublished - Sep 2010

Keywords

  • Hippo
  • TEAD
  • YAP
  • cancer
  • phosphorylation
  • structure

ASJC Scopus subject areas

  • Biotechnology
  • Biochemistry
  • Drug Discovery
  • Cell Biology

Fingerprint Dive into the research topics of 'Snapshots of a hybrid transcription factor in the Hippo pathway'. Together they form a unique fingerprint.

  • Cite this