Evidence map›Paper›PMID 32203417›Full record

ArticleNature cell biology2020

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

Yi Lu, Tiantian Wu, Orit Gutman, Huasong Lu, Qiang Zhou, Yoav I Henis, Kunxin Luo

Open access · greenAbstract read
In one paragraph

Article in Nature cell biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 225 papers.

0numbers the graph read from it
0cells of the map it votes in
225citing papers in PubMed
22.7field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

225 citing papers in PubMed, 367 citations in OpenAlex.

  1. The CTNNB1-TRIM28 complex governs hormone-induced RNA polymerase II dynamics in kidney epithelial cells.Proceedings of the National Academy of Sciences of the United States of America · 2026
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  5. Homer condensates orchestrate YAP-Wnt signaling crosstalk downstream of the Crumbs polarity complex.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
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  15. Investigating Phase Separation in Genome Folding via Multiscale Computational Modeling.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Review
  16. Article
  17. Article
  18. Article
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165 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 3 institutions in 3 countries.

Yi Lu *Department of Molecular and Cell Biology, University of California, Berkeley, Berkeley, CA, USA.
Tiantian Wu *Department of Molecular and Cell Biology, University of California, Berkeley, Berkeley, CA, USA.
Orit GutmanDepartment of Neurobiology, George S. Wise Faculty of Life Sciences, Tel Aviv University, Tel Aviv, Israel.
Huasong LuDepartment of Molecular and Cell Biology, University of California, Berkeley, Berkeley, CA, USA.
Qiang ZhouDepartment of Molecular and Cell Biology, University of California, Berkeley, Berkeley, CA, USA.
Yoav I HenisDepartment of Neurobiology, George S. Wise Faculty of Life Sciences, Tel Aviv University, Tel Aviv, Israel.ORCID http://orcid.org/0000-0002-1408-3877
Kunxin LuoDepartment of Molecular and Cell Biology, University of California, Berkeley, Berkeley, CA, USA. kluo@berkeley.edu.ORCID http://orcid.org/0000-0003-3711-2017
University of California, Berkeley · USTel Aviv University · ILXiamen University · CN

Funding

REGULATION OF TRANSCRIPTIONAL ELONGATION BY HIV1 TATR01AI041757 · NIAID · UNIVERSITY OF CALIFORNIA BERKELEY · PI ZHOU, QIANG · 1997 to 2019
$6.6M
NIAID NIH HHS R01 AI041757
6 · The paper itself

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.

Indexed as

Transcriptional ActivationBromodomain Containing ProteinsCell CompartmentationCell Cycle ProteinsCell Line, TumorCell Transformation, NeoplasticCyclin-Dependent Kinase 9DNA-Binding ProteinsHEK293 CellsHeLa CellsHumansMediator Complex Subunit 1Muscle ProteinsPhosphorylationProtein DomainsProtein Serine-Threonine KinasesBRD4 protein, humanBromodomain Containing ProteinsCDK9 protein, humanCell Cycle ProteinsCyclin-Dependent Kinase 9DNA-Binding ProteinsLATS1 protein, humanMED1 protein, humanMediator Complex Subunit 1Muscle ProteinsProtein Serine-Threonine KinasesTEAD4 protein, humanTEA Domain Transcription FactorsTrans-ActivatorsTranscriptional Coactivator with PDZ-Binding Motif ProteinsTranscription FactorsWWTR1 protein, human

Identifiers

PMID32203417
PMCPMC11044910
OpenAlexW3012720150

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.