Phase separation of TAZ compartmentalizes the transcription machinery to promote gene expression

Nat Cell Biol. 2020 Apr;22(4):453-464. doi: 10.1038/s41556-020-0485-0. Epub 2020 Mar 23.

Abstract

TAZ promotes growth, development and tumorigenesis by regulating the expression of target genes. However, the manner in which TAZ orchestrates the transcriptional responses is poorly defined. Here we demonstrate that TAZ forms nuclear condensates through liquid-liquid phase separation to compartmentalize its DNA-binding cofactor TEAD4, coactivators BRD4 and MED1, and the transcription elongation factor CDK9 for transcription. TAZ forms phase-separated droplets in vitro and liquid-like nuclear condensates in vivo, and this ability is negatively regulated by Hippo signalling through LATS-mediated phosphorylation and is mediated by the coiled-coil (CC) domain. Deletion of the TAZ CC domain or substitution with the YAP CC domain prevents the phase separation of TAZ and its ability to induce the expression of TAZ-specific target genes. Thus, we identify a mechanism of transcriptional activation by TAZ and demonstrate that pathway-specific transcription factors also engage the phase-separation mechanism for efficient and specific transcriptional activation.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Cell Compartmentation / genetics
  • Cell Cycle Proteins / genetics*
  • Cell Cycle Proteins / metabolism
  • Cell Line, Tumor
  • Cell Transformation, Neoplastic / genetics
  • Cell Transformation, Neoplastic / metabolism
  • Cyclin-Dependent Kinase 9 / genetics*
  • Cyclin-Dependent Kinase 9 / metabolism
  • DNA-Binding Proteins / genetics*
  • DNA-Binding Proteins / metabolism
  • HEK293 Cells
  • HeLa Cells
  • Humans
  • Mediator Complex Subunit 1 / genetics*
  • Mediator Complex Subunit 1 / metabolism
  • Muscle Proteins / genetics*
  • Muscle Proteins / metabolism
  • Phosphorylation
  • Protein Domains
  • Protein Serine-Threonine Kinases / genetics
  • Protein Serine-Threonine Kinases / metabolism
  • Signal Transduction
  • TEA Domain Transcription Factors
  • Trans-Activators / genetics*
  • Trans-Activators / metabolism
  • Transcription Factors / genetics*
  • Transcription Factors / metabolism
  • Transcriptional Activation*
  • Transcriptional Coactivator with PDZ-Binding Motif Proteins

Substances

  • BRD4 protein, human
  • Cell Cycle Proteins
  • DNA-Binding Proteins
  • MED1 protein, human
  • Mediator Complex Subunit 1
  • Muscle Proteins
  • TEA Domain Transcription Factors
  • TEAD4 protein, human
  • Trans-Activators
  • Transcription Factors
  • Transcriptional Coactivator with PDZ-Binding Motif Proteins
  • WWTR1 protein, human
  • LATS1 protein, human
  • Protein Serine-Threonine Kinases
  • CDK9 protein, human
  • Cyclin-Dependent Kinase 9